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Search results 1601 to 1700 out of 1964 for Hprt

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Categories

Category: Publication
Type Details Score
Publication  
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication  
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
Publication  
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication  
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication  
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
Publication
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
Publication
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
Publication  
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication  
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
Publication
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
Publication  
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
Publication  
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication
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
Publication  
First Author: Sigler AL
Year: 2024
Journal: Front Immunol
Title: FMNL1 and mDia1 promote efficient T cell migration through complex environments via distinct mechanisms.
Volume: 15
Pages: 1467415
Publication
First Author: Jain S
Year: 2008
Journal: Am J Physiol Regul Integr Comp Physiol
Title: A haplotype of human angiotensinogen gene containing -217A increases blood pressure in transgenic mice compared with -217G.
Volume: 295
Issue: 6
Pages: R1849-57
Publication
First Author: Kumar V
Year: 2016
Journal: J Allergy Clin Immunol
Title: Keratin-dependent thymic stromal lymphopoietin expression suggests a link between skin blistering and atopic disease.
Volume: 138
Issue: 5
Pages: 1461-1464.e6
Publication
First Author: Jackson WS
Year: 2013
Journal: Proc Natl Acad Sci U S A
Title: Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases.
Volume: 110
Issue: 36
Pages: 14759-64
Publication
First Author: Horev G
Year: 2011
Journal: Proc Natl Acad Sci U S A
Title: Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.
Volume: 108
Issue: 41
Pages: 17076-81
Publication
First Author: Tai DJC
Year: 2022
Journal: Am J Hum Genet
Title: Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models.
Volume: 109
Issue: 10
Pages: 1789-1813
Publication      
First Author: Yin X
Year: 2021
Journal: Nat Neurosci
Title: Delayed motor learning in a 16p11.2 deletion mouse model of autism is rescued by locus coeruleus activation.
Publication
First Author: Migliavacca E
Year: 2015
Journal: Am J Hum Genet
Title: A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology.
Volume: 96
Issue: 5
Pages: 784-96
Publication
First Author: Blumenthal I
Year: 2014
Journal: Am J Hum Genet
Title: Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.
Volume: 94
Issue: 6
Pages: 870-83
Publication
First Author: Goossens D
Year: 2010
Journal: Br J Haematol
Title: Generation and characterisation of Rhd and Rhag null mice.
Volume: 148
Issue: 1
Pages: 161-72
Publication
First Author: Lanza DG
Year: 2024
Journal: Genesis
Title: An oocyte-specific Cas9-expressing mouse for germline CRISPR/Cas9-mediated genome editing.
Volume: 62
Issue: 2
Pages: e23589
Publication
First Author: Bronson SK
Year: 1996
Journal: Proc Natl Acad Sci U S A
Title: Single-copy transgenic mice with chosen-site integration.
Volume: 93
Issue: 17
Pages: 9067-72
Publication
First Author: Yang H
Year: 2009
Journal: Blood
Title: Fibrinogen is required for maintenance of platelet intracellular and cell-surface P-selectin expression.
Volume: 114
Issue: 2
Pages: 425-36
Publication
First Author: Luo D
Year: 2013
Journal: J Immunol
Title: Fibrin facilitates both innate and T cell-mediated defense against Yersinia pestis.
Volume: 190
Issue: 8
Pages: 4149-61
Publication
First Author: Dong H
Year: 2013
Journal: Biochem Biophys Res Commun
Title: Mitochondrial targeting of mouse NQO1 and CYP1B1 proteins.
Volume: 435
Issue: 4
Pages: 727-32
Publication
First Author: Shibuya H
Year: 2014
Journal: Nat Cell Biol
Title: The TRF1-binding protein TERB1 promotes chromosome movement and telomere rigidity in meiosis.
Volume: 16
Issue: 2
Pages: 145-56
Publication
First Author: Ishibashi F
Year: 2018
Journal: Stem Cell Reports
Title: Contribution of ATOH1+ Cells to the Homeostasis, Repair, and Tumorigenesis of the Colonic Epithelium.
Volume: 10
Issue: 1
Pages: 27-42
Publication
First Author: Cheung AF
Year: 2010
Journal: Oncogene
Title: Complete deletion of Apc results in severe polyposis in mice.
Volume: 29
Issue: 12
Pages: 1857-64
Publication
First Author: Burr AR
Year: 2014
Journal: Mol Cell Biol
Title: Na+ dysregulation coupled with Ca2+ entry through NCX1 promotes muscular dystrophy in mice.
Volume: 34
Issue: 11
Pages: 1991-2002
Publication
First Author: Kuang S
Year: 2007
Journal: Cell
Title: Asymmetric self-renewal and commitment of satellite stem cells in muscle.
Volume: 129
Issue: 5
Pages: 999-1010
Publication
First Author: Sankaran JS
Year: 2016
Journal: Mamm Genome
Title: Modulation of unloading-induced bone loss in mice with altered ERK signaling.
Volume: 27
Issue: 1-2
Pages: 47-61
Publication
First Author: Loscher CJ
Year: 2008
Journal: Exp Eye Res
Title: A common microRNA signature in mouse models of retinal degeneration.
Volume: 87
Issue: 6
Pages: 529-34
Publication
First Author: Szabo R
Year: 2012
Journal: PLoS Genet
Title: Reduced prostasin (CAP1/PRSS8) activity eliminates HAI-1 and HAI-2 deficiency-associated developmental defects by preventing matriptase activation.
Volume: 8
Issue: 8
Pages: e1002937
Publication
First Author: Gras S
Year: 2016
Journal: Immunity
Title: Reversed T Cell Receptor Docking on a Major Histocompatibility Class I Complex Limits Involvement in the Immune Response.
Volume: 45
Issue: 4
Pages: 749-760
Publication
First Author: Linehan JL
Year: 2018
Journal: Cell
Title: Non-classical Immunity Controls Microbiota Impact on Skin Immunity and Tissue Repair.
Volume: 172
Issue: 4
Pages: 784-796.e18
Publication
First Author: Mendrysa SM
Year: 2003
Journal: Mol Cell Biol
Title: mdm2 Is critical for inhibition of p53 during lymphopoiesis and the response to ionizing irradiation.
Volume: 23
Issue: 2
Pages: 462-72
Publication
First Author: Grobe JL
Year: 2010
Journal: Hypertension
Title: Cardiovascular consequences of genetic variation at -6/235 in human angiotensinogen using "humanized" gene-targeted mice.
Volume: 56
Issue: 5
Pages: 981-7