Type |
Details |
Score |
Publication |
First Author: |
Ward CJ |
Year: |
1996 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Polycystin, the polycystic kidney disease 1 protein, is expressed by epithelial cells in fetal, adult, and polycystic kidney. |
Volume: |
93 |
Issue: |
4 |
Pages: |
1524-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Mochizuki T |
Year: |
1996 |
Journal: |
Science |
Title: |
PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein. |
Volume: |
272 |
Issue: |
5266 |
Pages: |
1339-42 |
|
•
•
•
•
•
|
Publication |
First Author: |
Veldhuisen B |
Year: |
1997 |
Journal: |
Am J Hum Genet |
Title: |
A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2). |
Volume: |
61 |
Issue: |
3 |
Pages: |
547-55 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
The REJ (Receptor for Egg Jelly) domain is found in PKD1 and the sperm receptor for egg jelly []. The exact function of this domain is unknown. The domain is 600 amino acids long so is probably composed of multiple structural domains. There are six completely conserved cysteine residues that may form disulphide bridges. This region contains tandem PKD-like domains.Sequence similarity between a region of the autosomal dominant polycystic kidney disease (ADPKD) protein, polycystin-1 and a sea urchin sperm glycoprotein involved in fertilization, the receptor for egg jelly (suREJ) has been known for some time. The suREJ protein binds the glycoprotein coat of the egg (egg jelly), triggering the acrosomereaction, which transforms the sperm into a fusogenic cell. The sequence similarity and expression pattern suggests that the predicted human PKDREJ protein is a mammalian equivalent of the suREJ protein and therefore may have a central role in human fertilization []. |
|
•
•
•
•
•
|
Publication |
First Author: |
Hughes J |
Year: |
1995 |
Journal: |
Nat Genet |
Title: |
The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains. |
Volume: |
10 |
Issue: |
2 |
Pages: |
151-60 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sumara G |
Year: |
2009 |
Journal: |
Cell |
Title: |
Regulation of PKD by the MAPK p38delta in insulin secretion and glucose homeostasis. |
Volume: |
136 |
Issue: |
2 |
Pages: |
235-48 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kim S |
Year: |
2016 |
Journal: |
Nat Cell Biol |
Title: |
The polycystin complex mediates Wnt/Ca(2+) signalling. |
Volume: |
18 |
Issue: |
7 |
Pages: |
752-764 |
|
•
•
•
•
•
|
Publication |
First Author: |
Nagano J |
Year: |
2005 |
Journal: |
Biochem Biophys Res Commun |
Title: |
Fibrocystin interacts with CAML, a protein involved in Ca2+ signaling. |
Volume: |
338 |
Issue: |
2 |
Pages: |
880-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Pennekamp P |
Year: |
1998 |
Journal: |
Mamm Genome |
Title: |
Characterization of the murine polycystic kidney disease (Pkd2) gene. |
Volume: |
9 |
Issue: |
9 |
Pages: |
749-52 |
|
•
•
•
•
•
|
Publication |
First Author: |
Avriyanti E |
Year: |
2015 |
Journal: |
Neurosci Res |
Title: |
Functional redundancy of protein kinase D1 and protein kinase D2 in neuronal polarity. |
Volume: |
95 |
|
Pages: |
12-20 |
|
•
•
•
•
•
|
Publication |
First Author: |
Park JE |
Year: |
2009 |
Journal: |
J Immunol |
Title: |
Protein kinase D1 is essential for MyD88-dependent TLR signaling pathway. |
Volume: |
182 |
Issue: |
10 |
Pages: |
6316-27 |
|
•
•
•
•
•
|
Publication |
First Author: |
Li X |
Year: |
2008 |
Journal: |
Nat Med |
Title: |
A tumor necrosis factor-alpha-mediated pathway promoting autosomal dominant polycystic kidney disease. |
Volume: |
14 |
Issue: |
8 |
Pages: |
863-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Liou GY |
Year: |
2015 |
Journal: |
Nat Commun |
Title: |
Protein kinase D1 drives pancreatic acinar cell reprogramming and progression to intraepithelial neoplasia. |
Volume: |
6 |
|
Pages: |
6200 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ngok SP |
Year: |
2012 |
Journal: |
J Cell Biol |
Title: |
VEGF and Angiopoietin-1 exert opposing effects on cell junctions by regulating the Rho GEF Syx. |
Volume: |
199 |
Issue: |
7 |
Pages: |
1103-15 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lantinga-van Leeuwen IS |
Year: |
2006 |
Journal: |
Genesis |
Title: |
Transgenic mice expressing tamoxifen-inducible Cre for somatic gene modification in renal epithelial cells. |
Volume: |
44 |
Issue: |
5 |
Pages: |
225-32 |
|
•
•
•
•
•
|
Publication |
First Author: |
White DP |
Year: |
2007 |
Journal: |
J Cell Biol |
Title: |
alpha v beta3 and alpha5beta1 integrin recycling pathways dictate downstream Rho kinase signaling to regulate persistent cell migration. |
Volume: |
177 |
Issue: |
3 |
Pages: |
515-25 |
|
•
•
•
•
•
|
Publication |
First Author: |
Germino GG |
Year: |
1990 |
Journal: |
Am J Hum Genet |
Title: |
Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16. |
Volume: |
46 |
Issue: |
5 |
Pages: |
925-33 |
|
•
•
•
•
•
|
Publication |
First Author: |
Medeiros RB |
Year: |
2005 |
Journal: |
Immunity |
Title: |
Protein kinase D1 and the beta 1 integrin cytoplasmic domain control beta 1 integrin function via regulation of Rap1 activation. |
Volume: |
23 |
Issue: |
2 |
Pages: |
213-26 |
|
•
•
•
•
•
|
Publication |
First Author: |
Oster H |
Year: |
2006 |
Journal: |
Gene Expr Patterns |
Title: |
Expression of the protein kinase D (PKD) family during mouse embryogenesis. |
Volume: |
6 |
Issue: |
4 |
Pages: |
400-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Park JE |
Year: |
2008 |
Journal: |
J Immunol |
Title: |
Protein kinase D1: a new component in TLR9 signaling. |
Volume: |
181 |
Issue: |
3 |
Pages: |
2044-55 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lee EC |
Year: |
2019 |
Journal: |
Nat Commun |
Title: |
Discovery and preclinical evaluation of anti-miR-17 oligonucleotide RGLS4326 for the treatment of polycystic kidney disease. |
Volume: |
10 |
Issue: |
1 |
Pages: |
4148 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kraus A |
Year: |
2016 |
Journal: |
Purinergic Signal |
Title: |
P2Y2R is a direct target of HIF-1α and mediates secretion-dependent cyst growth of renal cyst-forming epithelial cells. |
Volume: |
12 |
Issue: |
4 |
Pages: |
687-695 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
966
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
760
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
265
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
108
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Xu M |
Year: |
2013 |
Journal: |
J Biophys |
Title: |
Analysis of the REJ Module of Polycystin-1 Using Molecular Modeling and Force-Spectroscopy Techniques. |
Volume: |
2013 |
|
Pages: |
525231 |
|
•
•
•
•
•
|
Publication |
First Author: |
Rykx A |
Year: |
2003 |
Journal: |
FEBS Lett |
Title: |
Protein kinase D: a family affair. |
Volume: |
546 |
Issue: |
1 |
Pages: |
81-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Cobbaut M |
Year: |
2017 |
Journal: |
Sci Rep |
Title: |
Differential regulation of PKD isoforms in oxidative stress conditions through phosphorylation of a conserved Tyr in the P+1 loop. |
Volume: |
7 |
Issue: |
1 |
Pages: |
887 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
The polycystic kidney disease (PKD) domain is an 80-90 amino acid module originally found in 16 copies in the extracellular segment of polycystin-1, a large cell surface glycoprotein. Polycystin-1 is encoded by the PKD1 gene, which is mutated in autosomal dominant polycystic kidney disease (ADPKD).Although its function is unknown, it may be involved in protein-protein and protein-carbohydrate interactions based on its predicted domain structure. One or more copies of the PKD domain are also found in several other extracellular proteins from higher organisms, eubacteria, and archaebacteria. Singles copies of the PKD domain are found in the melanocytes heavily glycosylated cell-surface proteins Pmel 17, MMP and Nmp. Some bacterial collagenases and proteases also contain a single PKD domain adjacent to their catalytic domains, whereas four copies are present in the heavily glycosylated surface layer protein of archaebacteria []. The PKD modules are often observed, within a same protein sequence, in association with FnIII domains [].The most conserved motif is the WDFGDGS sequence that is found in the central part of many PKD domains and could play a structural role [, ]. Determination of the solution structure of the first PKD domain from human polycystin-1 has shown that the module is built from two β-sheet, one of three strands and one of four strands, which are packed face-to-face []. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
Protein phosphorylation, which plays a key role in most cellular activities, is a reversible process mediated by protein kinases and phosphoprotein phosphatases. Protein kinases catalyse the transfer of the gamma phosphate from nucleotide triphosphates (often ATP) to one or more amino acid residues in a protein substrate side chain, resulting in a conformational change affecting protein function. Phosphoprotein phosphatases catalyse the reverse process. Protein kinases fall into three broad classes, characterised with respect to substrate specificity []:Serine/threonine-protein kinasesTyrosine-protein kinasesDual specificity protein kinases (e.g. MEK - phosphorylates both Thr and Tyr on target proteins)Protein kinase function is evolutionarily conserved from Escherichia coli to human []. Protein kinases play a role in a multitude of cellular processes, including division, proliferation, apoptosis, and differentiation []. Phosphorylation usually results in a functional change of the target protein by changing enzyme activity, cellular location, or association with other proteins. The catalytic subunits of protein kinases are highly conserved, and several structures have been solved [], leading to large screens to develop kinase-specific inhibitors for the treatments of a number of diseases [].The protein kinase D family of enzymes consists of three isoforms: PKD1 (PKCmu), PKD2, and PKD3 (PKCnu). They all share a similar architecture with regulatory sub-domains that play specific roles in the activation, translocation and function of the enzymes. The PKD enzymes have recently been implicated in very diverse cellular functions, including Golgi organisation and plasma membrane directed transport, metastasis, immune responses, apoptosis and cell proliferation []. Each isoform is differentially regulated through phosphorylation []. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
Polycystic kidney diseases (PKD) are disorders characterised by large numbers of cysts distributed throughout grossly-enlarged kidneys. Cystdevelopment is associated with impairment of kidney function, and ultimately kidney failure and death [, ]. Most cases of autosomal dominant PKD result from mutations in the PKD1 gene that cause premature protein termination. A second gene for autosomal dominant polycystic kidney disease has been identified by positional cloning []. The predicted 968-amino acid sequence of the PKD2 gene product (polycystin-2) contains 6 transmembrane domains, with intracellular N- and C-termini. Polycystin-2 shares some similarity with the family of voltage-activated calcium (and sodium) channels, and contains a potential calcium-binding domain [].Polycystin-2 is strongly expressed in ovary, foetal and adult kidney, testis, and small intestine. Polycystin-1 requires the presence of this protein for stable expression and is believed to interact with it via its C terminus. All mutations between exons 1 and 11 result in a truncated polycystin-2 that lacks a calcium-binding EF-hand domain and the cytoplasmic domains required for the interaction of polycystin-2 with polycystin-1 []. PKD2, although clinically milder than PKD1, has a deleterious impact on life expectancy. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Homologous_superfamily |
Description: |
The polycystic kidney disease (PKD) domain is an 80-90 amino acid module originally found in 16 copies in the extracellular segment of polycystin-1, a large cell surface glycoprotein. Polycystin-1 is encoded by the PKD1 gene, which is mutated in autosomal dominant polycystic kidney disease (ADPKD).Although its function is unknown, it may be involved in protein-protein and protein-carbohydrate interactions based on its predicted domain structure. One or more copies of the PKD domain are also found in several other extracellular proteins from higher organisms, eubacteria, and archaebacteria. Singles copies of the PKD domain are found in the melanocytes heavily glycosylated cell-surface proteins Pmel 17, MMP and Nmp. Some bacterial collagenases and proteases also contain a single PKD domain adjacent to their catalytic domains, whereas four copies are present in the heavily glycosylated surface layer protein of archaebacteria []. The PKD modules are often observed, within a same protein sequence, in association with FnIII domains [].The most conserved motif is the WDFGDGS sequence that is found in the central part of many PKD domains and could play a structural role [, ]. Determination of the solution structure of the first PKD domain from human polycystin-1 has shown that the module is built from two β-sheet, one of three strands and one of four strands, which are packed face-to-face []. |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
349
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Callebaut I |
Year: |
2000 |
Journal: |
Protein Sci |
Title: |
HYR, an extracellular module involved in cellular adhesion and related to the immunoglobulin-like fold. |
Volume: |
9 |
Issue: |
7 |
Pages: |
1382-90 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
2126
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
2126
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Taglieri DM |
Year: |
2014 |
Journal: |
J Mol Cell Cardiol |
Title: |
The C-terminus of the long AKAP13 isoform (AKAP-Lbc) is critical for development of compensatory cardiac hypertrophy. |
Volume: |
66 |
|
Pages: |
27-40 |
|
•
•
•
•
•
|
Publication |
First Author: |
Gallagher AR |
Year: |
2000 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
The polycystic kidney disease protein PKD2 interacts with Hax-1, a protein associated with the actin cytoskeleton. |
Volume: |
97 |
Issue: |
8 |
Pages: |
4017-22 |
|
•
•
•
•
•
|
Publication |
First Author: |
Matthews SA |
Year: |
2010 |
Journal: |
Biochem J |
Title: |
Unique functions for protein kinase D1 and protein kinase D2 in mammalian cells. |
Volume: |
432 |
Issue: |
1 |
Pages: |
153-63 |
|
•
•
•
•
•
|
Publication |
First Author: |
Jensen ED |
Year: |
2009 |
Journal: |
J Biol Chem |
Title: |
Bone morphogenic protein 2 activates protein kinase D to regulate histone deacetylase 7 localization and repression of Runx2. |
Volume: |
284 |
Issue: |
4 |
Pages: |
2225-34 |
|
•
•
•
•
•
|
Publication |
First Author: |
Gallagher AR |
Year: |
2008 |
Journal: |
Am J Pathol |
Title: |
Biliary and pancreatic dysgenesis in mice harboring a mutation in Pkhd1. |
Volume: |
172 |
Issue: |
2 |
Pages: |
417-29 |
|
•
•
•
•
•
|
Publication |
First Author: |
Li A |
Year: |
2003 |
Journal: |
Genomics |
Title: |
Identification of two novel polycystic kidney disease-1-like genes in human and mouse genomes. |
Volume: |
81 |
Issue: |
6 |
Pages: |
596-608 |
|
•
•
•
•
•
|
Publication |
First Author: |
DeCaen PG |
Year: |
2013 |
Journal: |
Nature |
Title: |
Direct recording and molecular identification of the calcium channel of primary cilia. |
Volume: |
504 |
Issue: |
7479 |
Pages: |
315-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yuasa T |
Year: |
2002 |
Journal: |
Genomics |
Title: |
The sequence, expression, and chromosomal localization of a novel polycystic kidney disease 1-like gene, PKD1L1, in human. |
Volume: |
79 |
Issue: |
3 |
Pages: |
376-86 |
|
•
•
•
•
•
|
Publication |
First Author: |
Abdurrachim D |
Year: |
2017 |
Journal: |
Cardiovasc Res |
Title: |
Diabetic db/db mice do not develop heart failure upon pressure overload: a longitudinal in vivo PET, MRI, and MRS study on cardiac metabolic, structural, and functional adaptations. |
Volume: |
113 |
Issue: |
10 |
Pages: |
1148-1160 |
|
•
•
•
•
•
|
Publication |
First Author: |
Xiao Z |
Year: |
2014 |
Journal: |
PLoS One |
Title: |
Osteoblast-specific deletion of Pkd2 leads to low-turnover osteopenia and reduced bone marrow adiposity. |
Volume: |
9 |
Issue: |
12 |
Pages: |
e114198 |
|
•
•
•
•
•
|
Publication |
First Author: |
Prasad S |
Year: |
2009 |
Journal: |
Am J Pathol |
Title: |
Pkd2 dosage influences cellular repair responses following ischemia-reperfusion injury. |
Volume: |
175 |
Issue: |
4 |
Pages: |
1493-503 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ay M |
Year: |
2017 |
Journal: |
J Neurochem |
Title: |
Molecular mechanisms underlying protective effects of quercetin against mitochondrial dysfunction and progressive dopaminergic neurodegeneration in cell culture and MitoPark transgenic mouse models of Parkinson's Disease. |
Volume: |
141 |
Issue: |
5 |
Pages: |
766-782 |
|
•
•
•
•
•
|
Publication |
First Author: |
Zhou J |
Year: |
2009 |
Journal: |
Hum Mol Genet |
Title: |
Loss of Tsc1, but not Pten, in renal tubular cells causes polycystic kidney disease by activating mTORC1. |
Volume: |
18 |
Issue: |
22 |
Pages: |
4428-41 |
|
•
•
•
•
•
|
Publication |
First Author: |
Nomura H |
Year: |
1998 |
Journal: |
J Biol Chem |
Title: |
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects. |
Volume: |
273 |
Issue: |
40 |
Pages: |
25967-73 |
|
•
•
•
•
•
|
Publication |
First Author: |
Barone S |
Year: |
2021 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Kidney intercalated cells and the transcription factor FOXi1 drive cystogenesis in tuberous sclerosis complex. |
Volume: |
118 |
Issue: |
6 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Bhavanasi D |
Year: |
2011 |
Journal: |
Biochem Pharmacol |
Title: |
Protein kinase Cδ mediates the activation of protein kinase D2 in platelets. |
Volume: |
82 |
Issue: |
7 |
Pages: |
720-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Xiang SY |
Year: |
2013 |
Journal: |
Sci Signal |
Title: |
PLCε, PKD1, and SSH1L transduce RhoA signaling to protect mitochondria from oxidative stress in the heart. |
Volume: |
6 |
Issue: |
306 |
Pages: |
ra108 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kim MS |
Year: |
2008 |
Journal: |
Mol Cell Biol |
Title: |
Protein kinase D1 stimulates MEF2 activity in skeletal muscle and enhances muscle performance. |
Volume: |
28 |
Issue: |
11 |
Pages: |
3600-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ferdaoussi M |
Year: |
2012 |
Journal: |
Diabetologia |
Title: |
G protein-coupled receptor (GPR)40-dependent potentiation of insulin secretion in mouse islets is mediated by protein kinase D1. |
Volume: |
55 |
Issue: |
10 |
Pages: |
2682-2692 |
|
•
•
•
•
•
|
Publication |
First Author: |
Murphy TR |
Year: |
2007 |
Journal: |
J Immunol |
Title: |
Activation of protein kinase D1 in mast cells in response to innate, adaptive, and growth factor signals. |
Volume: |
179 |
Issue: |
11 |
Pages: |
7876-82 |
|
•
•
•
•
•
|
Publication |
First Author: |
Upadhyay K |
Year: |
2017 |
Journal: |
J Immunol |
Title: |
Group B Streptococci Induce Proinflammatory Responses via a Protein Kinase D1-Dependent Pathway. |
Volume: |
198 |
Issue: |
11 |
Pages: |
4448-4457 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kim YI |
Year: |
2010 |
Journal: |
J Immunol |
Title: |
Protein kinase D1 is essential for the proinflammatory response induced by hypersensitivity pneumonitis-causing thermophilic actinomycetes Saccharopolyspora rectivirgula. |
Volume: |
184 |
Issue: |
6 |
Pages: |
3145-56 |
|
•
•
•
•
•
|
Publication |
First Author: |
Fang X |
Year: |
2015 |
Journal: |
Prostate |
Title: |
Novel In Vivo model for combinatorial fluorescence labeling in mouse prostate. |
Volume: |
75 |
Issue: |
9 |
Pages: |
988-1000 |
|
•
•
•
•
•
|
Publication |
First Author: |
Li G |
Year: |
2021 |
Journal: |
Exp Cell Res |
Title: |
Adipose-specific knockout of Protein Kinase D1 suppresses de novo lipogenesis in mice via SREBP1c-dependent signaling. |
Volume: |
401 |
Issue: |
2 |
Pages: |
112548 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bossuyt J |
Year: |
2022 |
Journal: |
J Am Heart Assoc |
Title: |
Protein Kinase D1 Regulates Cardiac Hypertrophy, Potassium Channel Remodeling, and Arrhythmias in Heart Failure. |
Volume: |
11 |
Issue: |
19 |
Pages: |
e027573 |
|
•
•
•
•
•
|
Publication |
First Author: |
Rashel M |
Year: |
2014 |
Journal: |
J Invest Dermatol |
Title: |
Protein kinase D1 has a key role in wound healing and skin carcinogenesis. |
Volume: |
134 |
Issue: |
4 |
Pages: |
902-909 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hajarnis SS |
Year: |
2015 |
Journal: |
J Biol Chem |
Title: |
Transcription Factor Hepatocyte Nuclear Factor-1β (HNF-1β) Regulates MicroRNA-200 Expression through a Long Noncoding RNA. |
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290 |
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41 |
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24793-805 |
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First Author: |
Belyea BC |
Year: |
2023 |
Journal: |
Clin Sci (Lond) |
Title: |
Overexpression of notch signaling in renin cells leads to a polycystic kidney phenotype. |
Volume: |
137 |
Issue: |
1 |
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First Author: |
Löffler MC |
Year: |
2018 |
Journal: |
EMBO J |
Title: |
Protein kinase D1 deletion in adipocytes enhances energy dissipation and protects against adiposity. |
Volume: |
37 |
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22 |
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Publication |
First Author: |
Bergeron V |
Year: |
2018 |
Journal: |
Diabetes |
Title: |
Deletion of Protein Kinase D1 in Pancreatic β-Cells Impairs Insulin Secretion in High-Fat Diet-Fed Mice. |
Volume: |
67 |
Issue: |
1 |
Pages: |
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First Author: |
Yoon TW |
Year: |
2019 |
Journal: |
PLoS One |
Title: |
Ameliorating effects of Gö6976, a pharmacological agent that inhibits protein kinase D, on collagen-induced arthritis. |
Volume: |
14 |
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First Author: |
Ford JJ |
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2013 |
Journal: |
Endocrinology |
Title: |
Protein kinase D1 is essential for bone acquisition during pubertal growth. |
Volume: |
154 |
Issue: |
11 |
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Atik N |
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2014 |
Journal: |
Cell Struct Funct |
Title: |
The role of PKD in cell polarity, biosynthetic pathways, and organelle/F-actin distribution. |
Volume: |
39 |
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First Author: |
Butscheid Y |
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2006 |
Journal: |
Mol Reprod Dev |
Title: |
Polycystic kidney disease and receptor for egg jelly is a plasma membrane protein of mouse sperm head. |
Volume: |
73 |
Issue: |
3 |
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First Author: |
Molland KL |
Year: |
2010 |
Journal: |
Biochem J |
Title: |
Identification of the structural motif responsible for trimeric assembly of the C-terminal regulatory domains of polycystin channels PKD2L1 and PKD2. |
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Islam MR |
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2008 |
Journal: |
Am J Physiol Renal Physiol |
Title: |
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295 |
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2003 |
Journal: |
Am J Pathol |
Title: |
Polycystic kidney disease as a result of loss of the tuberous sclerosis 2 tumor suppressor gene during development. |
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2006 |
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Mol Cell Biol |
Title: |
Regulation of cardiac stress signaling by protein kinase d1. |
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26 |
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10 |
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First Author: |
Wilson SJ |
Year: |
2006 |
Journal: |
Biochim Biophys Acta |
Title: |
Inhibition of HER-2(neu/ErbB2) restores normal function and structure to polycystic kidney disease (PKD) epithelia. |
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1762 |
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7 |
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647-55 |
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Ellwanger K |
Year: |
2008 |
Journal: |
BMC Dev Biol |
Title: |
Expression patterns of protein kinase D 3 during mouse development. |
Volume: |
8 |
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Pages: |
47 |
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First Author: |
Yin DM |
Year: |
2008 |
Journal: |
J Neurosci |
Title: |
Both the establishment and maintenance of neuronal polarity require the activity of protein kinase D in the Golgi apparatus. |
Volume: |
28 |
Issue: |
35 |
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8832-43 |
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Publication |
First Author: |
Chen LA |
Year: |
2009 |
Journal: |
J Biol Chem |
Title: |
PKD3 is the predominant protein kinase D isoform in mouse exocrine pancreas and promotes hormone-induced amylase secretion. |
Volume: |
284 |
Issue: |
4 |
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2459-71 |
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First Author: |
Tsiokas L |
Year: |
2009 |
Journal: |
Am J Physiol Renal Physiol |
Title: |
Function and regulation of TRPP2 at the plasma membrane. |
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297 |
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1 |
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First Author: |
Wang Y |
Year: |
2019 |
Journal: |
J Biol Chem |
Title: |
Protein kinase D up-regulates transcription of VEGF receptor-2 in endothelial cells by suppressing nuclear localization of the transcription factor AP2β. |
Volume: |
294 |
Issue: |
43 |
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15759-15767 |
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First Author: |
Vijayakumar S |
Year: |
2014 |
Journal: |
Am J Physiol Renal Physiol |
Title: |
Aberrant expression of laminin-332 promotes cell proliferation and cyst growth in ARPKD. |
Volume: |
306 |
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6 |
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F640-54 |
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Publication |
First Author: |
Aicart-Ramos C |
Year: |
2014 |
Journal: |
J Cell Sci |
Title: |
Protein kinase D activity controls endothelial nitric oxide synthesis. |
Volume: |
127 |
Issue: |
Pt 15 |
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3360-72 |
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First Author: |
Jin X |
Year: |
2014 |
Journal: |
Biochim Biophys Acta |
Title: |
L-type calcium channel modulates cystic kidney phenotype. |
Volume: |
1842 |
Issue: |
9 |
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1518-26 |
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Publication |
First Author: |
Ryvkin V |
Year: |
2015 |
Journal: |
J Biol Chem |
Title: |
Opposing growth regulatory roles of protein kinase D isoforms in human keratinocytes. |
Volume: |
290 |
Issue: |
17 |
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11199-208 |
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Publication |
First Author: |
Müller M |
Year: |
2015 |
Journal: |
Sci Rep |
Title: |
A time frame permissive for Protein Kinase D2 activity to direct angiogenesis in mouse embryonic stem cells. |
Volume: |
5 |
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Pages: |
11742 |
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Publication |
First Author: |
Mazzeo C |
Year: |
2016 |
Journal: |
Cell Death Differ |
Title: |
Protein kinase D1/2 is involved in the maturation of multivesicular bodies and secretion of exosomes in T and B lymphocytes. |
Volume: |
23 |
Issue: |
1 |
Pages: |
99-109 |
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Publication |
First Author: |
Zhang B |
Year: |
2018 |
Journal: |
Development |
Title: |
Polycystin 1 loss of function is directly linked to an imbalance in G-protein signaling in the kidney. |
Volume: |
145 |
Issue: |
6 |
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Publication |
First Author: |
Lin CC |
Year: |
2018 |
Journal: |
Sci Rep |
Title: |
A cleavage product of Polycystin-1 is a mitochondrial matrix protein that affects mitochondria morphology and function when heterologously expressed. |
Volume: |
8 |
Issue: |
1 |
Pages: |
2743 |
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First Author: |
Merrick D |
Year: |
2019 |
Journal: |
Hum Mol Genet |
Title: |
Polycystin-1 regulates bone development through an interaction with the transcriptional coactivator TAZ. |
Volume: |
28 |
Issue: |
1 |
Pages: |
16-30 |
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Publication |
First Author: |
Czöndör K |
Year: |
2009 |
Journal: |
Mol Biol Cell |
Title: |
Protein kinase D controls the integrity of Golgi apparatus and the maintenance of dendritic arborization in hippocampal neurons. |
Volume: |
20 |
Issue: |
7 |
Pages: |
2108-20 |
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Publication |
First Author: |
Liliom H |
Year: |
2017 |
Journal: |
J Neurochem |
Title: |
Protein kinase D exerts neuroprotective functions during oxidative stress via nuclear factor kappa B-independent signaling pathways. |
Volume: |
142 |
Issue: |
6 |
Pages: |
948-961 |
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Publication |
First Author: |
Wang Z |
Year: |
2019 |
Journal: |
EMBO Rep |
Title: |
The ion channel function of polycystin-1 in the polycystin-1/polycystin-2 complex. |
Volume: |
20 |
Issue: |
11 |
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e48336 |
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Publication |
First Author: |
Kashyap P |
Year: |
2019 |
Journal: |
Biochem Biophys Res Commun |
Title: |
A PKD1L3 splice variant in taste buds is not cleaved at the G protein-coupled receptor proteolytic site. |
Volume: |
512 |
Issue: |
4 |
Pages: |
812-818 |
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Publication |
First Author: |
Suto JI |
Year: |
2019 |
Journal: |
J Genet |
Title: |
Genetic analysis of the mandible morphology in DDD.Cg-Ay/Sgn and C57BL/6J inbred mice. |
Volume: |
98 |
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First Author: |
Ding H |
Year: |
2021 |
Journal: |
Nat Commun |
Title: |
Extracellular vesicles and exosomes generated from cystic renal epithelial cells promote cyst growth in autosomal dominant polycystic kidney disease. |
Volume: |
12 |
Issue: |
1 |
Pages: |
4548 |
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Publication |
First Author: |
Sinnett-Smith J |
Year: |
2014 |
Journal: |
Am J Physiol Cell Physiol |
Title: |
Protein kinase D1 mediates class IIa histone deacetylase phosphorylation and nuclear extrusion in intestinal epithelial cells: role in mitogenic signaling. |
Volume: |
306 |
Issue: |
10 |
Pages: |
C961-71 |
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Publication |
First Author: |
Choudhary V |
Year: |
2014 |
Journal: |
J Dermatol Sci |
Title: |
Protein kinase D1 deficiency promotes differentiation in epidermal keratinocytes. |
Volume: |
76 |
Issue: |
3 |
Pages: |
186-95 |
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Publication |
First Author: |
de Stephanis L |
Year: |
2017 |
Journal: |
Clin Exp Nephrol |
Title: |
Double inhibition of cAMP and mTOR signalling may potentiate the reduction of cell growth in ADPKD cells. |
Volume: |
21 |
Issue: |
2 |
Pages: |
203-211 |
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Publication |
First Author: |
Dirkx E |
Year: |
2014 |
Journal: |
J Mol Cell Cardiol |
Title: |
Protein kinase-D1 overexpression prevents lipid-induced cardiac insulin resistance. |
Volume: |
76 |
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Pages: |
208-17 |
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