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Search results 3001 to 3100 out of 3442 for Hprt

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Type Details Score
Publication
26238780 | J:225885
First Author: Adams GN
Year: 2015
Journal: Cancer Res
Title: Colon Cancer Growth and Dissemination Relies upon Thrombin, Stromal PAR-1, and Fibrinogen.
Volume: 75
Issue: 19
Pages: 4235-43
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Publication
16877357 | J:310622
First Author: Adhami F
Year: 2006
Journal: Am J Pathol
Title: Cerebral ischemia-hypoxia induces intravascular coagulation and autophagy.
Volume: 169
Issue: 2
Pages: 566-83
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Publication
19036705 | J:145550
First Author: Reheman A
Year: 2009
Journal: Blood
Title: Plasma fibronectin depletion enhances platelet aggregation and thrombus formation in mice lacking fibrinogen and von Willebrand factor.
Volume: 113
Issue: 8
Pages: 1809-17
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Publication
14644995 | J:88569
First Author: Jirousková M
Year: 2004
Journal: Blood
Title: Antibody blockade or mutation of the fibrinogen gamma-chain C-terminus is more effective in inhibiting murine arterial thrombus formation than complete absence of fibrinogen.
Volume: 103
Issue: 6
Pages: 1995-2002
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Publication
17166882 | J:122123
First Author: Shertzer HG
Year: 2007
Journal: Carcinogenesis
Title: 7H-dibenzo[c,g]carbazole metabolism by the mouse and human CYP1 family of enzymes.
Volume: 28
Issue: 6
Pages: 1371-8
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Publication
19592578 | J:152846
First Author: Szabo R
Year: 2009
Journal: Development
Title: Regulation of cell surface protease matriptase by HAI2 is essential for placental development, neural tube closure and embryonic survival in mice.
Volume: 136
Issue: 15
Pages: 2653-63
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Publication
16397868 | J:105289
First Author: Wu MY
Year: 2006
Journal: Genesis
Title: Mouse imprinting defect mutations that model Angelman syndrome.
Volume: 44
Issue: 1
Pages: 12-22
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Publication
23974197 | J:203440
First Author: Gautier EL
Year: 2013
Journal: Blood
Title: Local apoptosis mediates clearance of macrophages from resolving inflammation in mice.
Volume: 122
Issue: 15
Pages: 2714-22
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Publication
18221731 | J:341304
First Author: Lawrence NJ
Year: 2008
Journal: DNA Repair (Amst)
Title: A neurological phenotype in mice with DNA repair gene Ercc1 deficiency.
Volume: 7
Issue: 2
Pages: 281-91
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Publication
23299312 | J:194757
First Author: Flick MJ
Year: 2013
Journal: Blood
Title: Genetic elimination of the binding motif on fibrinogen for the S. aureus virulence factor ClfA improves host survival in septicemia.
Volume: 121
Issue: 10
Pages: 1783-94
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Publication
25078604 | J:221394
First Author: Szabo R
Year: 2014
Journal: PLoS Genet
Title: Regulation of feto-maternal barrier by matriptase- and PAR-2-mediated signaling is required for placental morphogenesis and mouse embryonic survival.
Volume: 10
Issue: 7
Pages: e1004470
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Publication
21047530 | J:167359
First Author: Duchon A
Year: 2011
Journal: Behav Brain Res
Title: The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome.
Volume: 217
Issue: 2
Pages: 271-81
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Publication
20049703 | J:182796
First Author: Li HH
Year: 2009
Journal: EMBO Mol Med
Title: Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.
Volume: 1
Issue: 1
Pages: 50-65
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Strain
MGI:6241504 | B6.Cg-Abcc6<tm1c(EUCOMM)Wtsi> Speer6-ps1<Tg(Alb-cre)21Mgn> Tg(Cdx1-cre)23Kem
Attribute String: congenic, mutant strain, targeted mutation, transgenic
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Publication
37595802 | J:340545
First Author: Bradić I
Year: 2023
Journal: J Lipid Res
Title: Metabolic changes and propensity for inflammation, fibrosis, and cancer in livers of mice lacking lysosomal acid lipase.
Volume: 64
Issue: 9
Pages: 100427
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Publication
27782803 | J:239418
First Author: Corso-Díaz X
Year: 2016
Journal: BMC Genomics
Title: Co-activator candidate interactions for orphan nuclear receptor NR2E1.
Volume: 17
Issue: 1
Pages: 832
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Publication
17591625 | J:167506
First Author: Besson V
Year: 2007
Journal: Hum Mol Genet
Title: Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responses.
Volume: 16
Issue: 17
Pages: 2040-52
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Publication
22215611 | J:320775
First Author: Bode B
Year: 2011
Journal: J Biol Rhythms
Title: Genetic interaction of Per1 and Dec1/2 in the regulation of circadian locomotor activity.
Volume: 26
Issue: 6
Pages: 530-40
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Publication
26884601 | J:260274
First Author: Viel S
Year: 2016
Journal: Sci Signal
Title: TGF-β inhibits the activation and functions of NK cells by repressing the mTOR pathway.
Volume: 9
Issue: 415
Pages: ra19
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Publication
22251704 | J:184496
First Author: Anson M
Year: 2012
Journal: J Clin Invest
Title: Oncogenic β-catenin triggers an inflammatory response that determines the aggressiveness of hepatocellular carcinoma in mice.
Volume: 122
Issue: 2
Pages: 586-99
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Publication
22855808 | J:186626
First Author: Trivedi D
Year: 2012
Journal: J Neurosci
Title: Live-cell imaging evidence for the ciliary transport of rod photoreceptor opsin by heterotrimeric kinesin-2.
Volume: 32
Issue: 31
Pages: 10587-93
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Publication
12782655 | J:83740
First Author: Oster H
Year: 2003
Journal: Genes Dev
Title: Loss of circadian rhythmicity in aging mPer1-/-mCry2-/- mutant mice.
Volume: 17
Issue: 11
Pages: 1366-79
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Publication
20824053 | J:165024
 
First Author: Jud C
Year: 2010
Journal: PLoS One
Title: High amplitude phase resetting in rev-erbalpha/per1 double mutant mice.
Volume: 5
Issue: 9
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Publication
26561650 | J:281411
First Author: Alnasser HA
Year: 2016
Journal: Am J Physiol Renal Physiol
Title: Requirement of clusterin expression for prosurvival autophagy in hypoxic kidney tubular epithelial cells.
Volume: 310
Issue: 2
Pages: F160-73
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Publication
28701379 | J:244424
First Author: Wojtas AM
Year: 2017
Journal: Proc Natl Acad Sci U S A
Title: Loss of clusterin shifts amyloid deposition to the cerebrovasculature via disruption of perivascular drainage pathways.
Volume: 114
Issue: 33
Pages: E6962-E6971
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Publication
25660546 | J:247640
First Author: Shi SQ
Year: 2015
Journal: Curr Biol
Title: Ube3a imprinting impairs circadian robustness in Angelman syndrome models.
Volume: 25
Issue: 5
Pages: 537-45
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Publication
15643613 | J:96716
First Author: Jiang Z
Year: 2005
Journal: Hum Mutat
Title: Toward the evaluation of function in genetic variability: characterizing human SNP frequencies and establishing BAC-transgenic mice carrying the human CYP1A1_CYP1A2 locus.
Volume: 25
Issue: 2
Pages: 196-206
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Publication
22935098 | J:225088
First Author: Curran CP
Year: 2012
Journal: Neurotoxicology
Title: Ahrd Cyp1a2(-/-) mice show increased susceptibility to PCB-induced developmental neurotoxicity.
Volume: 33
Issue: 6
Pages: 1436-42
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Publication
28759001 | J:259143
First Author: Gao Y
Year: 2017
Journal: Nat Immunol
Title: Tumor immunoevasion by the conversion of effector NK cells into type 1 innate lymphoid cells.
Volume: 18
Issue: 9
Pages: 1004-1015
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Publication
31402618 | J:355139
First Author: Deguise MO
Year: 2019
Journal: Ann Clin Transl Neurol
Title: Abnormal fatty acid metabolism is a core component of spinal muscular atrophy.
Volume: 6
Issue: 8
Pages: 1519-1532
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Publication
29614705 | J:278710
First Author: Setter DO
Year: 2018
Journal: Restor Neurol Neurosci
Title: Identification of a resilient mouse facial motoneuron population following target disconnection by injury or disease.
Volume: 36
Issue: 3
Pages: 417-422
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Publication
23736297 | J:201095
First Author: Ravenscroft G
Year: 2013
Journal: Hum Mol Genet
Title: Cardiac α-actin over-expression therapy in dominant ACTA1 disease.
Volume: 22
Issue: 19
Pages: 3987-97
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Publication
28229533 | J:241523
First Author: Flores RR
Year: 2017
Journal: Aging Cell
Title: Expansion of myeloid-derived suppressor cells with aging in the bone marrow of mice through a NF-κB-dependent mechanism.
Volume: 16
Issue: 3
Pages: 480-487
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Publication
31060774 | J:291747
First Author: Custer SK
Year: 2019
Journal: Biochem Biophys Res Commun
Title: Interaction between alpha-COP and SMN ameliorates disease phenotype in a mouse model of spinal muscular atrophy.
Volume: 514
Issue: 2
Pages: 530-537
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Publication
26506088 | J:355106
First Author: Somers E
Year: 2016
Journal: Ann Neurol
Title: Vascular Defects and Spinal Cord Hypoxia in Spinal Muscular Atrophy.
Volume: 79
Issue: 2
Pages: 217-30
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Publication
24405637 | J:355161
 
First Author: Hadwen J
Year: 2014
Journal: Orphanet J Rare Dis
Title: VPAC2 receptor agonist BAY 55-9837 increases SMN protein levels and moderates disease phenotype in severe spinal muscular atrophy mouse models.
Volume: 9
Pages: 4
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Publication
36291733 | J:348133
 
First Author: Franco-Espin J
Year: 2022
Journal: Biomolecules
Title: SMN Is Physiologically Downregulated at Wild-Type Motor Nerve Terminals but Aggregates Together with Neurofilaments in SMA Mouse Models.
Volume: 12
Issue: 10
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Publication
31777926 | J:285124
First Author: Pagliarini V
Year: 2020
Journal: Nucleic Acids Res
Title: Sam68 binds Alu-rich introns in SMN and promotes pre-mRNA circularization.
Volume: 48
Issue: 2
Pages: 633-645
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Publication
27488123 | J:237935
First Author: Miller N
Year: 2016
Journal: Hum Mol Genet
Title: Motor neuron mitochondrial dysfunction in spinal muscular atrophy.
Volume: 25
Issue: 16
Pages: 3395-3406
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Publication
37976261 | J:355053
First Author: Miller N
Year: 2023
Journal: Proc Natl Acad Sci U S A
Title: Mitigating aberrant Cdk5 activation alleviates mitochondrial defects and motor neuron disease symptoms in spinal muscular atrophy.
Volume: 120
Issue: 47
Pages: e2300308120
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Publication
10655541 | J:60592
First Author: Monani UR
Year: 2000
Journal: Hum Mol Genet
Title: The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy.
Volume: 9
Issue: 3
Pages: 333-9
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Publication
23736298 | J:201094
First Author: Gogliotti RG
Year: 2013
Journal: Hum Mol Genet
Title: The DcpS inhibitor RG3039 improves survival, function and motor unit pathologies in two SMA mouse models.
Volume: 22
Issue: 20
Pages: 4084-101
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Publication
17020410 | J:116054
First Author: Andressoo JO
Year: 2006
Journal: PLoS Biol
Title: Rescue of progeria in trichothiodystrophy by homozygous lethal Xpd alleles.
Volume: 4
Issue: 10
Pages: e322
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Publication
29961886 | J:355100
First Author: Janzen E
Year: 2018
Journal: Brain
Title: CHP1 reduction ameliorates spinal muscular atrophy pathology by restoring calcineurin activity and endocytosis.
Volume: 141
Issue: 8
Pages: 2343-2361
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Publication
35902978 | J:327146
First Author: Meijboom KE
Year: 2022
Journal: Skelet Muscle
Title: Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy mice.
Volume: 12
Issue: 1
Pages: 18
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Publication
35041705 | J:322483
First Author: Negrón O
Year: 2022
Journal: PLoS Pathog
Title: Fibrin(ogen) engagement of S. aureus promotes the host antimicrobial response and suppression of microbe dissemination following peritoneal infection.
Volume: 18
Issue: 1
Pages: e1010227
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Publication
18821589 | J:148747
First Author: Bartholin L
Year: 2008
Journal: Genesis
Title: Generation of mice with conditionally activated transforming growth factor beta signaling through the TbetaRI/ALK5 receptor.
Volume: 46
Issue: 12
Pages: 724-31
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Publication
25523394 | J:218835
First Author: Lane J
Year: 2015
Journal: Dev Biol
Title: Tak1, Smad4 and Trim33 redundantly mediate TGF-β3 signaling during palate development.
Volume: 398
Issue: 2
Pages: 231-41
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Publication
17623673 | J:125022
First Author: Madsen DH
Year: 2007
Journal: J Biol Chem
Title: Extracellular collagenases and the endocytic receptor, urokinase plasminogen activator receptor-associated protein/Endo180, cooperate in fibroblast-mediated collagen degradation.
Volume: 282
Issue: 37
Pages: 27037-45
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8075633 | J:23827
First Author: Green LL
Year: 1994
Journal: Nat Genet
Title: Antigen-specific human monoclonal antibodies from mice engineered with human Ig heavy and light chain YACs.
Volume: 7
Issue: 1
Pages: 13-21
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Publication
19458618 | J:150286
First Author: Baek KH
Year: 2009
Journal: Nature
Title: Down's syndrome suppression of tumour growth and the role of the calcineurin inhibitor DSCR1.
Volume: 459
Issue: 7250
Pages: 1126-30
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Publication
17517686 | J:125089
First Author: Bi W
Year: 2007
Journal: Hum Mol Genet
Title: Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.
Volume: 16
Issue: 15
Pages: 1802-13
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Publication
17218265 | J:117887
First Author: Wallace HA
Year: 2007
Journal: Cell
Title: Manipulating the mouse genome to engineer precise functional syntenic replacements with human sequence.
Volume: 128
Issue: 1
Pages: 197-209
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10517636 | J:57757
First Author: Lindsay EA
Year: 1999
Journal: Nature
Title: Congenital heart disease in mice deficient for the DiGeorge syndrome region.
Volume: 401
Issue: 6751
Pages: 379-83
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22219321 | J:180742
First Author: Alcaide P
Year: 2012
Journal: J Immunol
Title: Difference in Th1 and Th17 lymphocyte adhesion to endothelium.
Volume: 188
Issue: 3
Pages: 1421-30
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Publication
19709627 | J:154937
First Author: Jackson WS
Year: 2009
Journal: Neuron
Title: Spontaneous generation of prion infectivity in fatal familial insomnia knockin mice.
Volume: 63
Issue: 4
Pages: 438-50
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Publication
22586121 | J:184755
First Author: Durand A
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Functional intestinal stem cells after Paneth cell ablation induced by the loss of transcription factor Math1 (Atoh1).
Volume: 109
Issue: 23
Pages: 8965-70
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Publication
24466234 | J:206207
First Author: Shin M
Year: 2014
Journal: PLoS One
Title: Matrix metalloproteinase-20 over-expression is detrimental to enamel development: a Mus musculus model.
Volume: 9
Issue: 1
Pages: e86774
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Publication
22243238 | J:268514
 
First Author: Smith CE
Year: 2011
Journal: Eur J Oral Sci
Title: Relationships between protein and mineral during enamel development in normal and genetically altered mice.
Volume: 119 Suppl 1
Pages: 125-35
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Publication
26432904 | J:293071
First Author: Lazelle RA
Year: 2016
Journal: J Am Soc Nephrol
Title: Renal Deletion of 12 kDa FK506-Binding Protein Attenuates Tacrolimus-Induced Hypertension.
Volume: 27
Issue: 5
Pages: 1456-64
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Publication
22139080 | J:187869
First Author: Kosa P
Year: 2012
Journal: Oncogene
Title: Suppression of Tumorigenicity-14, encoding matriptase, is a critical suppressor of colitis and colitis-associated colon carcinogenesis.
Volume: 31
Issue: 32
Pages: 3679-95
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Publication
22370638 | J:193376
First Author: van der Weyden L
Year: 2013
Journal: Oncogene
Title: Jdp2 downregulates Trp53 transcription to promote leukaemogenesis in the context of Trp53 heterozygosity.
Volume: 32
Issue: 3
Pages: 397-402
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Publication
26286849 | J:230254
First Author: Arumugam PI
Year: 2015
Journal: Blood
Title: Genetic diminution of circulating prothrombin ameliorates multiorgan pathologies in sickle cell disease mice.
Volume: 126
Issue: 15
Pages: 1844-55
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Publication
31624228 | J:294529
First Author: Oron O
Year: 2019
Journal: Transl Psychiatry
Title: Gene network analysis reveals a role for striatal glutamatergic receptors in dysregulated risk-assessment behavior of autism mouse models.
Volume: 9
Issue: 1
Pages: 257
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Publication
26273832 | J:242778
First Author: Brunner D
Year: 2015
Journal: PLoS One
Title: Comprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder.
Volume: 10
Issue: 8
Pages: e0134572
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Publication
32853769 | J:331666
First Author: Nuzzo T
Year: 2020
Journal: Biochim Biophys Acta Proteins Proteom
Title: Dysfunctional d-aspartate metabolism in BTBR mouse model of idiopathic autism.
Volume: 1868
Issue: 12
Pages: 140531
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Publication
36127322 | J:331677
First Author: Carey C
Year: 2022
Journal: Transl Psychiatry
Title: From bench to bedside: The mGluR5 system in people with and without Autism Spectrum Disorder and animal model systems.
Volume: 12
Issue: 1
Pages: 395
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Publication
30282698 | J:266417
 
First Author: Horder J
Year: 2018
Journal: Sci Transl Med
Title: GABAA receptor availability is not altered in adults with autism spectrum disorder or in mouse models.
Volume: 10
Issue: 461
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Publication
27385010 | J:235722
First Author: Szabo R
Year: 2016
Journal: Development
Title: Delineation of proteolytic and non-proteolytic functions of the membrane-anchored serine protease prostasin.
Volume: 143
Issue: 15
Pages: 2818-28
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Publication
28397107 | J:279639
First Author: Rubio ME
Year: 2017
Journal: Brain Struct Funct
Title: The number and distribution of AMPA receptor channels containing fast kinetic GluA3 and GluA4 subunits at auditory nerve synapses depend on the target cells.
Volume: 222
Issue: 8
Pages: 3375-3393
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Publication
38067144 | J:343417
 
First Author: Fang X
Year: 2023
Journal: Cells
Title: Sertoli Cell-Specific Activation of Transforming Growth Factor Beta Receptor 1 Leads to Testicular Granulosa Cell Tumor Formation.
Volume: 12
Issue: 23
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Publication
26304725 | J:227530
First Author: Parisi A
Year: 2015
Journal: J Cell Biol
Title: APC is required for muscle stem cell proliferation and skeletal muscle tissue repair.
Volume: 210
Issue: 5
Pages: 717-26
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Publication
25347473 | J:219414
First Author: Funato Y
Year: 2014
Journal: J Clin Invest
Title: Membrane protein CNNM4-dependent Mg2+ efflux suppresses tumor progression.
Volume: 124
Issue: 12
Pages: 5398-410
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Publication
29439001 | J:263054
First Author: Balbinot C
Year: 2018
Journal: J Exp Med
Title: The Cdx2 homeobox gene suppresses intestinal tumorigenesis through non-cell-autonomous mechanisms.
Volume: 215
Issue: 3
Pages: 911-926
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Publication
36639541 | J:333939
First Author: Säisä-Borreill S
Year: 2023
Journal: Cell Death Differ
Title: General transcription factor TAF4 antagonizes epigenetic silencing by Polycomb to maintain intestine stem cell functions.
Volume: 30
Issue: 3
Pages: 839-853
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Publication
36545778 | J:341371
First Author: Prieto S
Year: 2023
Journal: EMBO Rep
Title: CDK8 and CDK19 act redundantly to control the CFTR pathway in the intestinal epithelium.
Volume: 24
Issue: 2
Pages: e54261
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Publication
32213541 | J:288817
First Author: Bruschi M
Year: 2020
Journal: Cancer Res
Title: Loss of Apc Rapidly Impairs DNA Methylation Programs and Cell Fate Decisions in Lgr5+ Intestinal Stem Cells.
Volume: 80
Issue: 11
Pages: 2101-2113
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Publication
30888356 | J:331986
First Author: Jin L
Year: 2019
Journal: Metallomics
Title: Mice overexpressing hepcidin suggest ferroportin does not play a major role in Mn homeostasis.
Volume: 11
Issue: 5
Pages: 959-967
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Publication
28462381 | J:332142
First Author: Frazer DM
Year: 2017
Journal: Cell Mol Gastroenterol Hepatol
Title: Ferroportin Is Essential for Iron Absorption During Suckling, But Is Hyporesponsive to the Regulatory Hormone Hepcidin.
Volume: 3
Issue: 3
Pages: 410-421
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Publication
24952462 | J:219389
First Author: Whissell G
Year: 2014
Journal: Nat Cell Biol
Title: The transcription factor GATA6 enables self-renewal of colon adenoma stem cells by repressing BMP gene expression.
Volume: 16
Issue: 7
Pages: 695-707
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Publication
19549529 | J:172956
First Author: Zagani R
Year: 2009
Journal: Gastroenterology
Title: Cyclooxygenase-2 inhibitors down-regulate osteopontin and Nr4A2-new therapeutic targets for colorectal cancers.
Volume: 137
Issue: 4
Pages: 1358-66.e1-3
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Publication
16488993 | J:106660
First Author: Andreu P
Year: 2006
Journal: Cancer Res
Title: Identification of the IFITM family as a new molecular marker in human colorectal tumors.
Volume: 66
Issue: 4
Pages: 1949-55
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Publication
29930175 | J:308958
 
First Author: Hiratsuka S
Year: 2018
Journal: EMBO Mol Med
Title: Hepato-entrained B220+CD11c+NK1.1+ cells regulate pre-metastatic niche formation in the lung.
Volume: 10
Issue: 7
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Publication
34292972 | J:308480
First Author: Wu Y
Year: 2021
Journal: PLoS One
Title: The effects of Cstb duplication on APP/amyloid-β pathology and cathepsin B activity in a mouse model.
Volume: 16
Issue: 7
Pages: e0242236
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Publication
24244869 | J:227962
 
First Author: Nusayr E
Year: 2013
Journal: Physiol Rep
Title: FGF2 modulates cardiac remodeling in an isoform- and sex-specific manner.
Volume: 1
Issue: 4
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Publication
24244870 | J:227961
 
First Author: Nusayr E
Year: 2013
Journal: Physiol Rep
Title: Cardiac development and physiology are modulated by FGF2 in an isoform- and sex-specific manner.
Volume: 1
Issue: 4
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Publication
21124890 | J:170239
First Author: Ricard G
Year: 2010
Journal: PLoS Biol
Title: Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models.
Volume: 8
Issue: 11
Pages: e1000543
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Publication
17273973 | J:125240
First Author: Yan J
Year: 2007
Journal: Am J Hum Genet
Title: Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike.
Volume: 80
Issue: 3
Pages: 518-25
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Publication
22654670 | J:185193
First Author: Lacaria M
Year: 2012
Journal: PLoS Genet
Title: A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men.
Volume: 8
Issue: 5
Pages: e1002713
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Publication
30550590 | J:269755
First Author: Ni N
Year: 2018
Journal: PLoS One
Title: Glandular defects in the mouse uterus with sustained activation of TGF-beta signaling is associated with altered differentiation of endometrial stromal cells and formation of stromal compartment.
Volume: 13
Issue: 12
Pages: e0209417
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Publication
37149866 | J:335872
First Author: Béland-Millar A
Year: 2023
Journal: Cell Rep
Title: 16p11.2 haploinsufficiency reduces mitochondrial biogenesis in brain endothelial cells and alters brain metabolism in adult mice.
Volume: 42
Issue: 5
Pages: 112485
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17202262 | J:119071
First Author: Prosser HM
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Prokineticin receptor 2 (Prokr2) is essential for the regulation of circadian behavior by the suprachiasmatic nuclei.
Volume: 104
Issue: 2
Pages: 648-53
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Publication
39628570 | J:359305
First Author: Choi A
Year: 2024
Journal: iScience
Title: Circuit mechanism underlying fragmented sleep and memory deficits in 16p11.2 deletion mouse model of autism.
Volume: 27
Issue: 12
Pages: 111285
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29465786 | J:262032
First Author: Akiyoshi S
Year: 2018
Journal: Eur J Neurosci
Title: Subpopulations of vomeronasal sensory neurons with coordinated coexpression of type 2 vomeronasal receptor genes are differentially dependent on Vmn2r1.
Volume: 47
Issue: 7
Pages: 887-900
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28916757 | J:243630
First Author: Bosnakovski D
Year: 2017
Journal: Nat Commun
Title: Muscle pathology from stochastic low level DUX4 expression in an FSHD mouse model.
Volume: 8
Issue: 1
Pages: 550
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Strain
MGI:5690043 | B6.129S7-Del(16Dyrk1a-Kcnj6)14Yey/Dp(16Lipi-Zbtb21)1Yey
Attribute String: chromosome aberration, congenic, deletion, duplication, mutant strain
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Strain
MGI:5690036 | B6.129S7-Del(16Kcnj15-Mx2)13Yey/Dp(16Lipi-Zbtb21)1Yey
Attribute String: mutant strain, duplication, deletion, congenic, chromosome aberration
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Strain
MGI:5690030 | B6.129S7-Del(16Setd4-Kcnj6)12Yey/Dp(16Lipi-Zbtb21)1Yey
Attribute String: chromosome aberration, congenic, deletion, duplication, mutant strain
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Strain
MGI:5689553 | B6.129S7-Del(16Dyrk1a-Kcnj6)14Yey/Dp(16Lipi-Zbtb21)1Yey/J
Attribute String: deletion, congenic, mutant strain, targeted mutation
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Strain
MGI:5689540 | B6;129S7-Del(16Setd4-Kcnj6)12Yey/Dp(16Lipi-Zbtb21)1Yey/J
Attribute String: duplication, targeted mutation, deletion, mutant stock
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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