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Search results 1001 to 1100 out of 1146 for Pkd1

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Type Details Score
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
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: 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: 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: 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: 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: 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: 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: 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: 71-77
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: 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: 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: 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.
Volume: 290
Issue: 41
Pages: 24793-805
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: 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: Löffler MC
Year: 2018
Journal: EMBO J
Title: Protein kinase D1 deletion in adipocytes enhances energy dissipation and protects against adiposity.
Volume: 37
Issue: 22
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: 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
Pages: 35-45
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: 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
Issue: 12
Pages: e0226145
Publication
First Author: Atik N
Year: 2014
Journal: Cell Struct Funct
Title: The role of PKD in cell polarity, biosynthetic pathways, and organelle/F-actin distribution.
Volume: 39
Issue: 1
Pages: 61-77
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: 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: Ford JJ
Year: 2013
Journal: Endocrinology
Title: Protein kinase D1 is essential for bone acquisition during pubertal growth.
Volume: 154
Issue: 11
Pages: 4182-91
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: 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: 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.
Volume: 429
Issue: 1
Pages: 171-83
Publication
First Author: Islam MR
Year: 2008
Journal: Am J Physiol Renal Physiol
Title: Retinoic acid-dependent activation of the polycystic kidney disease-1 (PKD1) promoter.
Volume: 295
Issue: 6
Pages: F1845-54
Publication
First Author: Butscheid Y
Year: 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
Pages: 350-60
Publication
First Author: Cai S
Year: 2003
Journal: Am J Pathol
Title: Polycystic kidney disease as a result of loss of the tuberous sclerosis 2 tumor suppressor gene during development.
Volume: 162
Issue: 2
Pages: 457-68
Publication
First Author: Harrison BC
Year: 2006
Journal: Mol Cell Biol
Title: Regulation of cardiac stress signaling by protein kinase d1.
Volume: 26
Issue: 10
Pages: 3875-88
Publication
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.
Volume: 1762
Issue: 7
Pages: 647-55
Publication  
First Author: Ellwanger K
Year: 2008
Journal: BMC Dev Biol
Title: Expression patterns of protein kinase D 3 during mouse development.
Volume: 8
Pages: 47
Publication
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
Pages: 8832-43
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
Pages: 2459-71
Publication
First Author: Tsiokas L
Year: 2009
Journal: Am J Physiol Renal Physiol
Title: Function and regulation of TRPP2 at the plasma membrane.
Volume: 297
Issue: 1
Pages: F1-9
Publication
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
Pages: 15759-15767
Publication
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
Issue: 6
Pages: F640-54
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
Pages: 3360-72
Publication
First Author: Jin X
Year: 2014
Journal: Biochim Biophys Acta
Title: L-type calcium channel modulates cystic kidney phenotype.
Volume: 1842
Issue: 9
Pages: 1518-26
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
Pages: 11199-208
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
Pages: 11742
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
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
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
Publication
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
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
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
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
Pages: e48336
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
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
Publication
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
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
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
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
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
Pages: 208-17
Publication
First Author: Yao Q
Year: 2021
Journal: FASEB J
Title: Polycystin-1 dependent regulation of polycystin-2 via GRP94, a member of HSP90 family that resides in the endoplasmic reticulum.
Volume: 35
Issue: 10
Pages: e21865
Publication  
First Author: Chou LF
Year: 2018
Journal: Nutrients
Title: Effect of Trehalose Supplementation on Autophagy and Cystogenesis in a Mouse Model of Polycystic Kidney Disease.
Volume: 11
Issue: 1
Publication
First Author: Dong K
Year: 2021
Journal: Nat Genet
Title: Renal plasticity revealed through reversal of polycystic kidney disease in mice.
Volume: 53
Issue: 12
Pages: 1649-1663
Protein
Organism: Mus musculus/domesticus
Length: 2126  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 2126  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 2201  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 217  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 2151  
Fragment?: false
Publication
First Author: Vogel P
Year: 2010
Journal: Vet Pathol
Title: Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice.
Volume: 47
Issue: 1
Pages: 120-31
Publication  
First Author: Mira Hernandez J
Year: 2023
Journal: J Mol Cell Cardiol
Title: Cardiac Protein Kinase D1 ablation alters the myocytes β-adrenergic response.
Volume: 180
Pages: 33-43
Publication
First Author: Yuan J
Year: 2008
Journal: Am J Physiol Gastrointest Liver Physiol
Title: Protein kinase D1 mediates NF-kappaB activation induced by cholecystokinin and cholinergic signaling in pancreatic acinar cells.
Volume: 295
Issue: 6
Pages: G1190-201
Publication
First Author: Alcalay NI
Year: 2008
Journal: Am J Physiol Renal Physiol
Title: Acceleration of polycystic kidney disease progression in cpk mice carrying a deletion in the homeodomain protein Cux1.
Volume: 295
Issue: 6
Pages: F1725-34
Publication
First Author: Sinnett-Smith J
Year: 2011
Journal: J Biol Chem
Title: Protein kinase D1 mediates stimulation of DNA synthesis and proliferation in intestinal epithelial IEC-18 cells and in mouse intestinal crypts.
Volume: 286
Issue: 1
Pages: 511-20
Publication
First Author: Chiou YS
Year: 2013
Journal: Carcinogenesis
Title: Peracetylated (-)-epigallocatechin-3-gallate (AcEGCG) potently prevents skin carcinogenesis by suppressing the PKD1-dependent signaling pathway in CD34+ skin stem cells and skin tumors.
Volume: 34
Issue: 6
Pages: 1315-22
Publication
First Author: Eckberg K
Year: 2022
Journal: Am J Physiol Renal Physiol
Title: Small hairpin inhibitory RNA delivery in the metanephric organ culture identifies long noncoding RNA Pvt1 as a modulator of cyst growth.
Volume: 323
Issue: 3
Pages: F335-F348
Protein
Organism: Mus musculus/domesticus
Length: 574  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 1048  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 1081  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 626  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 419  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 838  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 574  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 626  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 526  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 574  
Fragment?: false