Global Gene Expression Analysis of Murine Limb Development
暂无分享,去创建一个
[1] G. Wagner,et al. Transcriptomic analysis of avian digits reveals conserved and derived digit identities in birds , 2011, Nature.
[2] Ben Xu,et al. Axial Hox9 activity establishes the posterior field in the developing forelimb , 2011, Proceedings of the National Academy of Sciences.
[3] A. Yoshiki,et al. Suppression of cell-cycle progression by Jun dimerization protein-2 (JDP2) involves downregulation of cyclin-A2 , 2010, Oncogene.
[4] J. Drouin,et al. Divergent transcriptional activities determine limb identity , 2010, Nature communications.
[5] D. Keene,et al. In Vivo Studies of Mutant Fibrillin-1 Microfibrils* , 2010, The Journal of Biological Chemistry.
[6] Miao Wang,et al. Targeted Mutation of the Mouse Grp94 Gene Disrupts Development and Perturbs Endoplasmic Reticulum Stress Signaling , 2010, PloS one.
[7] Jarema Malicki,et al. The Apical Complex Couples Cell Fate and Cell Survival to Cerebral Cortical Development , 2010, Neuron.
[8] Y. Ishikawa,et al. Prolyl 3-Hydroxylase 1 Null Mice Display Abnormalities in Fibrillar Collagen-rich Tissues Such as Tendons, Skin, and Bones* , 2010, The Journal of Biological Chemistry.
[9] T. Blanpied,et al. Cortactin is implicated in murine zygotic development. , 2010, Experimental cell research.
[10] S. Phadke,et al. Polydactyly and genes , 2010, Indian journal of pediatrics.
[11] Á. Valverde,et al. Normal Proliferation and Tumorigenesis but Impaired Pancreatic Function in Mice Lacking the Cell Cycle Regulator Sei1 , 2010, PloS one.
[12] C. Sotelo,et al. Progressive Purkinje Cell Degeneration in tambaleante Mutant Mice Is a Consequence of a Missense Mutation in HERC1 E3 Ubiquitin Ligase , 2009, PLoS genetics.
[13] Takeshi Kimura,et al. Fibulin-4 conducts proper elastogenesis via interaction with cross-linking enzyme lysyl oxidase , 2009, Proceedings of the National Academy of Sciences of the United States of America.
[14] J. Nathans,et al. Norrin, Frizzled-4, and Lrp5 Signaling in Endothelial Cells Controls a Genetic Program for Retinal Vascularization , 2009, Cell.
[15] E. Li,et al. KDM1B is a histone H3K4 demethylase required to establish maternal genomic imprints , 2009, Nature.
[16] S. Alper,et al. Deletion of the Chloride Transporter Slc26a7 Causes Distal Renal Tubular Acidosis and Impairs Gastric Acid Secretion* , 2009, The Journal of Biological Chemistry.
[17] J. Brüning,et al. Riboflavin kinase couples TNF receptor 1 to NADPH oxidase , 2009, Nature.
[18] K. Molne,et al. Spontaneous adrenocortical lipid depletion in mice. Relationship to general growth, degeneration of adrenal X zone, and maturation of seminiferous eptthelium. , 2009, Acta pathologica et microbiologica Scandinavica.
[19] A. Malmström,et al. Dermatan Sulfate Epimerase 1-Deficient Mice Have Reduced Content and Changed Distribution of Iduronic Acids in Dermatan Sulfate and an Altered Collagen Structure in Skin , 2009, Molecular and Cellular Biology.
[20] H. Westphal,et al. LIM homeobox transcription factors integrate signaling events that control three-dimensional limb patterning and growth , 2009, Development.
[21] B. Peterlin,et al. Cyclin T2 Is Essential for Mouse Embryogenesis , 2009, Molecular and Cellular Biology.
[22] Yi Zhang,et al. Role of Jhdm2a in regulating metabolic gene expression and obesity resistance , 2009, Nature.
[23] Randy L. Johnson,et al. Lmx1b‐expressing cells in the mouse limb bud define a dorsal mesenchymal lineage compartment , 2009, Genesis.
[24] J. Milbrandt,et al. AMP-activated protein kinase phosphorylates retinoblastoma protein to control mammalian brain development. , 2009, Developmental cell.
[25] Yu-Qiang Ding,et al. Manifold functions of the Nail‐Patella Syndrome gene Lmx1b in vertebrate development , 2009, Development, growth & differentiation.
[26] P. Chambon,et al. Induction of thymic stromal lymphopoietin expression in keratinocytes is necessary for generating an atopic dermatitis upon application of the active vitamin D3 analogue MC903 on mouse skin. , 2009, The Journal of investigative dermatology.
[27] G. Sumara,et al. Regulation of PKD by the MAPK p38δ in Insulin Secretion and Glucose Homeostasis , 2009, Cell.
[28] Matthew Towers,et al. Growing models of vertebrate limb development , 2009, Development.
[29] Ananda L Roy,et al. Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development , 2009, Proceedings of the National Academy of Sciences.
[30] J. Crish,et al. Mast Cells Contribute to Autoimmune Inflammatory Arthritis via Their Tryptase/Heparin Complexes1 , 2009, The Journal of Immunology.
[31] H. Kiyonari,et al. Short limbs, cleft palate, and delayed formation of flat proliferative chondrocytes in mice with targeted disruption of a putative protein kinase gene, Pkdcc (AW548124) , 2009, Developmental dynamics : an official publication of the American Association of Anatomists.
[32] Audrey Kauffmann,et al. Bioinformatics Applications Note Arrayqualitymetrics—a Bioconductor Package for Quality Assessment of Microarray Data , 2022 .
[33] Yuan-Tsong Chen,et al. Mutations in the SLC2A10 gene cause arterial abnormalities in mice. , 2008, Cardiovascular research.
[34] S. Bartling,et al. A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions. , 2008, Human molecular genetics.
[35] R. Finn,et al. Defining the in Vivo Role for Cytochrome b5 in Cytochrome P450 Function through the Conditional Hepatic Deletion of Microsomal Cytochrome b5*S⃞ , 2008, Journal of Biological Chemistry.
[36] P. Leder,et al. A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints. , 2008, Developmental cell.
[37] D. Ferguson,et al. Mre11 Nuclease Activity Has Essential Roles in DNA Repair and Genomic Stability Distinct from ATM Activation , 2008, Cell.
[38] R. Pope,et al. Role of H2-calponin in Regulating Macrophage Motility and Phagocytosis* , 2008, Journal of Biological Chemistry.
[39] T. Mak,et al. Beyond tumor necrosis factor receptor: TRADD signaling in toll-like receptors , 2008, Proceedings of the National Academy of Sciences.
[40] E. Willems,et al. An optimized procedure for whole-mount in situ hybridization on mouse embryos and embryoid bodies , 2008, Nature Protocols.
[41] K. Takeda,et al. Regulation of adult erythropoiesis by prolyl hydroxylase domain proteins. , 2008, Blood.
[42] Bon-Kyoung Koo,et al. Crif1 is a novel transcriptional coactivator of STAT3 , 2008, The EMBO journal.
[43] Kenji Nakamura,et al. Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta , 2008, Nature Genetics.
[44] F. Murakami,et al. The role of Slit-Robo signaling in the generation, migration and morphological differentiation of cortical interneurons. , 2008, Developmental biology.
[45] W. Griffiths,et al. Deletion of a xenobiotic metabolizing gene in mice affects folate metabolism , 2007, Biochemical and biophysical research communications.
[46] A. Hirao,et al. Neural-specific ablation of the scaffold protein JSAP1 in mice causes neonatal death , 2007, Neuroscience Letters.
[47] Richard T. Lee,et al. Targeted Deletion of Thioredoxin-Interacting Protein Regulates Cardiac Dysfunction in Response to Pressure Overload , 2007, Circulation research.
[48] C. Blagden,et al. Synaptic differentiation is defective in mice lacking acetylcholine receptor β-subunit tyrosine phosphorylation , 2007, Development.
[49] M. Capecchi,et al. Hoxc10 and Hoxd10 regulate mouse columnar, divisional and motor pool identity of lumbar motoneurons , 2007, Development.
[50] B. Malissen,et al. Deletion of the LIME adaptor protein minimally affects T and B cell development and function , 2007, European journal of immunology.
[51] L. Birnbaumer,et al. Attenuation of store-operated Ca2+ current impairs salivary gland fluid secretion in TRPC1(−/−) mice , 2007, Proceedings of the National Academy of Sciences.
[52] Eric Verdin,et al. Mammalian Sir2 Homolog SIRT3 Regulates Global Mitochondrial Lysine Acetylation , 2007, Molecular and Cellular Biology.
[53] T. Seki,et al. Evolutionarily Conserved Mammalian Adenine Nucleotide Translocase 4 Is Essential for Spermatogenesis* , 2007, Journal of Biological Chemistry.
[54] J. Favor,et al. Genetic, biochemical, and molecular characterization of nine glyceraldehyde-3-phosphate dehydrogenase mutants with reduced enzyme activity in Mus musculus , 2007, Mammalian Genome.
[55] D. Heinegård,et al. Reduced cell proliferation and increased apoptosis are significant pathological mechanisms in a murine model of mild pseudoachondroplasia resulting from a mutation in the C-terminal domain of COMP. , 2007, Human molecular genetics.
[56] M. McKee,et al. Endocrine Regulation of Energy Metabolism by the Skeleton , 2007, Cell.
[57] M. Bang,et al. Structural and regulatory roles of muscle ankyrin repeat protein family in skeletal muscle. , 2007, American journal of physiology. Cell physiology.
[58] H. Okuno,et al. Regulation of Dendritogenesis via a Lipid-Raft-Associated Ca2+/Calmodulin-Dependent Protein Kinase CLICK-III/CaMKIγ , 2007, Neuron.
[59] Hidde L Ploegh,et al. The mouse polyubiquitin gene UbC is essential for fetal liver development, cell‐cycle progression and stress tolerance , 2007, The EMBO journal.
[60] M. Pagano,et al. The After-Hours Mutant Reveals a Role for Fbxl3 in Determining Mammalian Circadian Period , 2007, Science.
[61] Baoxue Yang,et al. Reduced urea flux across the blood-testis barrier and early maturation in the male reproductive system in UT-B-null mice. , 2007, American journal of physiology. Cell physiology.
[62] Xinhua Lin,et al. Pygo1 and Pygo2 roles in Wnt signaling in mammalian kidney development , 2007, BMC Biology.
[63] R. Bank,et al. Tissue-specific Changes in the Hydroxylysine Content and Cross-links of Collagens and Alterations in Fibril Morphology in Lysyl Hydroxylase 1 Knock-out Mice* , 2007, Journal of Biological Chemistry.
[64] P. Bagnoli,et al. Changes in neuronal response to ischemia in retinas with genetic alterations of somatostatin receptor expression , 2007, The European journal of neuroscience.
[65] D. Carson,et al. Global growth deficiencies in mice lacking the ribosomal protein HIP/RPL29 , 2007, Developmental dynamics : an official publication of the American Association of Anatomists.
[66] Linda Yang,et al. Cdc42 GTPase-activating protein deficiency promotes genomic instability and premature aging-like phenotypes , 2007, Proceedings of the National Academy of Sciences.
[67] V. Papaioannou,et al. Tbx4 is not required for hindlimb identity or post-bud hindlimb outgrowth , 2007, Development.
[68] K. An,et al. TGFbeta inducible early gene-1 knockout mice display defects in bone strength and microarchitecture. , 2006, Bone.
[69] Marc Tessier-Lavigne,et al. Boc is a receptor for sonic hedgehog in the guidance of commissural axons , 2006, Nature.
[70] M. Hediger,et al. Marked Disturbance of Calcium Homeostasis in Mice With Targeted Disruption of the Trpv6 Calcium Channel Gene , 2006, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[71] Nan Tang,et al. Essential role of RGS-PX1/sorting nexin 13 in mouse development and regulation of endocytosis dynamics , 2006, Proceedings of the National Academy of Sciences.
[72] G. Martin,et al. Cochlear developmental defect and background-dependent hearing thresholds in the Jackson circler (jc) mutant mouse , 2006, Hearing Research.
[73] Barbara Cannon,et al. Ablation of PGC-1β Results in Defective Mitochondrial Activity, Thermogenesis, Hepatic Function, and Cardiac Performance , 2006, PLoS biology.
[74] J. Partanen,et al. Targeted Deletion of the Muscular Dystrophy Gene myotilin Does Not Perturb Muscle Structure or Function in Mice , 2006, Molecular and Cellular Biology.
[75] Yali Dou,et al. Coactivator as a target gene specificity determinant for histone H3 lysine 4 methyltransferases , 2006, Proceedings of the National Academy of Sciences.
[76] P. Hawkins,et al. PtdIns3P binding to the PX domain of p40phox is a physiological signal in NADPH oxidase activation , 2006, The EMBO journal.
[77] M. Cheeseman,et al. Sexually dimorphic expression of secreted frizzled‐related (SFRP) genes in the developing mouse Müllerian duct , 2006, Molecular reproduction and development.
[78] P. Carmeliet,et al. Selective regulation of arterial branching morphogenesis by synectin. , 2006, Developmental cell.
[79] K. Mikoshiba,et al. Decreased basal mucus secretion by Slp2‐a‐deficient gastric surface mucous cells , 2006, Genes to cells : devoted to molecular & cellular mechanisms.
[80] Charles J Malemud,et al. Matrix metalloproteinases (MMPs) in health and disease: an overview. , 2006, Frontiers in bioscience : a journal and virtual library.
[81] N. Ropert,et al. Mice Lacking Brain/Kidney Phosphate-Activated Glutaminase Have Impaired Glutamatergic Synaptic Transmission, Altered Breathing, Disorganized Goal-Directed Behavior and Die Shortly after Birth , 2006, The Journal of Neuroscience.
[82] R. Coleman,et al. Agpat6—a novel lipid biosynthetic gene required for triacylglycerol production in mammary epithelium Published, JLR Papers in Press, January 31, 2006. , 2006, Journal of Lipid Research.
[83] T. Jacques,et al. Essential role for hematopoietic prostaglandin D2 synthase in the control of delayed type hypersensitivity. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[84] D. Duboule,et al. A mouse model for human short-stature syndromes identifies Shox2 as an upstream regulator of Runx2 during long-bone development. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[85] Kimberly C. Smith,et al. Dynamic Anchoring of PKA Is Essential during Oocyte Maturation , 2006, Current Biology.
[86] Marc Flajolet,et al. Alterations in 5-HT1B Receptor Function by p11 in Depression-Like States , 2006, Science.
[87] Rudolf Grosschedl,et al. EBF2 regulates osteoblast-dependent differentiation of osteoclasts. , 2005, Developmental cell.
[88] Abdul Waheed,et al. Carbonic anhydrase IV and XIV knockout mice: roles of the respective carbonic anhydrases in buffering the extracellular space in brain. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[89] R. Mcinnes,et al. The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development. , 2005, Developmental biology.
[90] Crispin J. Miller,et al. Simpleaffy: a BioConductor package for Affymetrix Quality Control and data analysis , 2005, Bioinform..
[91] J. R. Holt,et al. Fast Adaptation in Vestibular Hair Cells Requires Myosin-1c Activity , 2005, Neuron.
[92] N. Joyce,et al. The FASEB Journal • Research Communication Targeted disruption of Col8a1 and Col8a2 genes in mice leads to anterior segment abnormalities in the eye , 2022 .
[93] J. Decaprio,et al. Dimerization of CUL7 and PARC Is Not Required for All CUL7 Functions and Mouse Development , 2005, Molecular and Cellular Biology.
[94] Takashi Tanaka,et al. SLIM is a nuclear ubiquitin E3 ligase that negatively regulates STAT signaling. , 2005, Immunity.
[95] F. Rieke,et al. Recoverin Improves Rod-Mediated Vision by Enhancing Signal Transmission in the Mouse Retina , 2005, Neuron.
[96] K. Irie,et al. Roles of cell-adhesion molecules nectin 1 and nectin 3 in ciliary body development , 2005, Development.
[97] M. Barbacid,et al. Protein farnesyltransferase in embryogenesis, adult homeostasis, and tumor development. , 2005, Cancer cell.
[98] V. Sheffield,et al. Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[99] M. Capecchi,et al. Pax 3 : Fkhr interferes with embryonic Pax 3 and Pax 7 function : implications for alveolar rhabdomyosarcoma cell of origin , 2004 .
[100] Jean YH Yang,et al. Bioconductor: open software development for computational biology and bioinformatics , 2004, Genome Biology.
[101] M. Lu,et al. Advanced Cardiac Morphogenesis Does Not Require Heart Tube Fusion , 2004, Science.
[102] T. Anthony,et al. Preservation of Liver Protein Synthesis during Dietary Leucine Deprivation Occurs at the Expense of Skeletal Muscle Mass in Mice Deleted for eIF2 Kinase GCN2* , 2004, Journal of Biological Chemistry.
[103] M. Tsai,et al. RabGEF1 is a negative regulator of mast cell activation and skin inflammation , 2004, Nature Immunology.
[104] Chengyu Liu,et al. Cyclic nucleotide phosphodiesterase 3A-deficient mice as a model of female infertility. , 2004, The Journal of clinical investigation.
[105] C. Sardet,et al. The E4F Protein Is Required for Mitotic Progression during Embryonic Cell Cycles , 2004, Molecular and Cellular Biology.
[106] J. Hiltunen,et al. A mouse model for alpha-methylacyl-CoA racemase deficiency: adjustment of bile acid synthesis and intolerance to dietary methyl-branched lipids. , 2004, Human molecular genetics.
[107] Dean Y. Li,et al. Ccm1 is required for arterial morphogenesis: implications for the etiology of human cavernous malformations , 2004, Development.
[108] Hong Lei,et al. Histone H3-K9 Methyltransferase ESET Is Essential for Early Development , 2004, Molecular and Cellular Biology.
[109] T. Rabbitts,et al. Null Mutation of the Lmo4 Gene or a Combined Null Mutation of the Lmo1/Lmo3 Genes Causes Perinatal Lethality, and Lmo4 Controls Neural Tube Development in Mice , 2004, Molecular and Cellular Biology.
[110] R. Bronson,et al. Loss of NFAT5 results in renal atrophy and lack of tonicity-responsive gene expression. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[111] E. Morii,et al. Identification of a Cytokine-induced Antiapoptotic Molecule Anamorsin Essential for Definitive Hematopoiesis , 2004, The Journal of experimental medicine.
[112] Gordon K Smyth,et al. Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments , 2004, Statistical applications in genetics and molecular biology.
[113] Benjamin M. Bolstad,et al. affy - analysis of Affymetrix GeneChip data at the probe level , 2004, Bioinform..
[114] S. Linn,et al. DDB2 gene disruption leads to skin tumors and resistance to apoptosis after exposure to ultraviolet light but not a chemical carcinogen , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[115] D. Dix,et al. Genomic Instability and Enhanced Radiosensitivity in Hsp70.1- and Hsp70.3-Deficient Mice , 2004, Molecular and Cellular Biology.
[116] D. Lohnes,et al. Retinoic acid regulates a subset of Cdx1 function in vivo , 2003, Development.
[117] C. Rogler,et al. Reduced hepatocyte proliferation is the basis of retarded liver tumor progression and liver regeneration in mice lacking N-acetylglucosaminyltransferase III. , 2003, Cancer research.
[118] B. Bruneau,et al. The Iroquois Homeobox Gene Irx2 Is Not Essential for Normal Development of the Heart and Midbrain-Hindbrain Boundary in Mice , 2003, Molecular and Cellular Biology.
[119] P. Roughley,et al. Genetic Rescue of Chondrodysplasia and the Perinatal Lethal Effect of Cartilage Link Protein Deficiency* , 2003, Journal of Biological Chemistry.
[120] X. Deng,et al. Disruption of the COP9 Signalosome Csn2 Subunit in Mice Causes Deficient Cell Proliferation, Accumulation of p53 and Cyclin E, and Early Embryonic Death , 2003, Molecular and Cellular Biology.
[121] Raul Urrutia,et al. KRAB-containing zinc-finger repressor proteins , 2003, Genome Biology.
[122] Franz Vauti,et al. A large-scale, gene-driven mutagenesis approach for the functional analysis of the mouse genome , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[123] M. Åbrink,et al. Targeted Disruption of a Murine Glucuronyl C5-epimerase Gene Results in Heparan Sulfate Lacking l-Iduronic Acid and in Neonatal Lethality* , 2003, Journal of Biological Chemistry.
[124] T. Magnuson,et al. H1 Linker Histones Are Essential for Mouse Development and Affect Nucleosome Spacing In Vivo , 2003, Molecular and Cellular Biology.
[125] J. Hoeijmakers,et al. A novel regulation mechanism of DNA repair by damage-induced and RAD23-dependent stabilization of xeroderma pigmentosum group C protein. , 2003, Genes & development.
[126] M. Glogauer,et al. Rac1 Deletion in Mouse Neutrophils Has Selective Effects on Neutrophil Functions1 , 2003, The Journal of Immunology.
[127] G. Martin,et al. Deciphering skeletal patterning: clues from the limb , 2003, Nature.
[128] C. McKerlie,et al. Targeted Disruption of the ATP2A1 Gene Encoding the Sarco(endo)plasmic Reticulum Ca2+ ATPase Isoform 1 (SERCA1) Impairs Diaphragm Function and Is Lethal in Neonatal Mice* , 2003, The Journal of Biological Chemistry.
[129] Yuqiong Liang,et al. The zinc-finger protein CNBP is required for forebrain formation in the mouse , 2003, Development.
[130] S. Akira,et al. TAB2 Is Essential for Prevention of Apoptosis in Fetal Liver but Not for Interleukin-1 Signaling , 2003, Molecular and Cellular Biology.
[131] Terence P. Speed,et al. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias , 2003, Bioinform..
[132] S. Krauss,et al. Targeted disruption of mouse Dach1 results in postnatal lethality , 2003, Developmental dynamics : an official publication of the American Association of Anatomists.
[133] S. Akira,et al. Negative Regulation of Platelet Clearance and of the Macrophage Phagocytic Response by the Transmembrane Glycoprotein SHPS-1* , 2002, The Journal of Biological Chemistry.
[134] Arthur M Buchberg,et al. A novel transgenic line of mice exhibiting autosomal recessive male-specific lethality and non-alcoholic fatty liver disease. , 2002, Human molecular genetics.
[135] B. de Strooper,et al. The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts. , 2002, Human molecular genetics.
[136] B. S. Baker,et al. Gene Expression During the Life Cycle of Drosophila melanogaster , 2002, Science.
[137] I. Kola,et al. Mice Lacking Glutathione Peroxidase-1 Activity Show Increased Tunel Staining and an Accelerated Inflammatory Response in Brain Following a Cold-Induced Injury , 2002, Experimental Neurology.
[138] M. Burmeister,et al. Mutation of a novel gene results in abnormal development of spermatid flagella, loss of intermale aggression and reduced body fat in mice. , 2002, Genetics.
[139] J. Piatigorsky,et al. Transketolase Haploinsufficiency Reduces Adipose Tissue and Female Fertility in Mice , 2002, Molecular and Cellular Biology.
[140] S. Nishikawa,et al. Elbow knee synostosis (Eks): a new mutation on mouse Chromosome 14 , 2002, Mammalian Genome.
[141] N. Copeland,et al. Mitf and Tfe3, two members of the Mitf-Tfe family of bHLH-Zip transcription factors, have important but functionally redundant roles in osteoclast development , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[142] Wei Li,et al. Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene , 2002, Nature Genetics.
[143] J. Hartwig,et al. WIP deficiency reveals a differential role for WIP and the actin cytoskeleton in T and B cell activation. , 2002, Immunity.
[144] D. Rifkin,et al. Bone abnormalities in latent TGF-β binding protein (Ltbp)-3–null mice indicate a role for Ltbp-3 in modulating TGF-β bioavailability , 2002, The Journal of cell biology.
[145] D. A. O’Brien,et al. Germ Cell Survival Through Carbohydrate-Mediated Interaction with Sertoli Cells , 2002, Science.
[146] D. Prockop,et al. Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: Comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED) , 2001, Developmental dynamics : an official publication of the American Association of Anatomists.
[147] B. Spiegelman,et al. Adipose tissue reduction in mice lacking the translational inhibitor 4E-BP1 , 2001, Nature Medicine.
[148] G. Martin,et al. Making a vertebrate limb: new players enter from the wings. , 2001, BioEssays : news and reviews in molecular, cellular and developmental biology.
[149] E. H. Margulies,et al. A comparative molecular analysis of developing mouse forelimbs and hindlimbs using serial analysis of gene expression (SAGE). , 2001, Genome research.
[150] R. Chadwick,et al. Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein-methyltransferase superfamily. , 2001, Genes & development.
[151] Paul Scherz,et al. Functional analysis of secreted and transmembrane proteins critical to mouse development , 2001, Nature Genetics.
[152] J. Dennis,et al. Late mitotic failure in mice lacking Sak, a polo-like kinase , 2001, Current Biology.
[153] A. Chishti,et al. Disruption of the Mouse μ-Calpain Gene Reveals an Essential Role in Platelet Function , 2001, Molecular and Cellular Biology.
[154] Kenji Nakamura,et al. Sez4 gene encoding an elongation subunit of DNA polymerase ζ is required for normal embryogenesis , 2001, Genes to cells : devoted to molecular & cellular mechanisms.
[155] R. Harland,et al. Mutation and Analysis of Dan, the Founding Member of the Dan Family of Transforming Growth Factor β Antagonists , 2001, Molecular and Cellular Biology.
[156] J. P. Hobson,et al. Edg-1, the G protein-coupled receptor for sphingosine-1-phosphate, is essential for vascular maturation. , 2000, The Journal of clinical investigation.
[157] Jason G. Cyster,et al. A chemokine-driven positive feedback loop organizes lymphoid follicles , 2000, Nature.
[158] M. Roussel,et al. Disruption of the ARF transcriptional activator DMP1 facilitates cell immortalization, Ras transformation, and tumorigenesis. , 2000, Genes & development.
[159] Margaret A. Johns,et al. Mice deficient in the candidate tumor suppressor gene Hic1 exhibit developmental defects of structures affected in the Miller-Dieker syndrome. , 2000, Human molecular genetics.
[160] G. Kay,et al. Mice lacking the vascular endothelial growth factor-B gene (Vegfb) have smaller hearts, dysfunctional coronary vasculature, and impaired recovery from cardiac ischemia. , 2000, Circulation research.
[161] J. Naggert,et al. Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene. , 2000, Human molecular genetics.
[162] Scott A. Rifkin,et al. Microarray analysis of Drosophila development during metamorphosis. , 1999, Science.
[163] M. Rice,et al. Disruption of muREC2/RAD51L1 in Mice Results in Early Embryonic Lethality Which Can Be Partially Rescued in a p53−/− Background , 1999, Molecular and Cellular Biology.
[164] M. Evans,et al. A retroviral gene trap insertion into the histone 3.3A gene causes partial neonatal lethality, stunted growth, neuromuscular deficits and male sub-fertility in transgenic mice. , 1999, Human molecular genetics.
[165] A. Bradley,et al. Congenital heart disease in mice deficient for the DiGeorge syndrome region , 1999, Nature.
[166] G. Oliver,et al. Prox1 Function Is Required for the Development of the Murine Lymphatic System , 1999, Cell.
[167] Concepción Rodríguez-Esteban,et al. The T-box genes Tbx4 and Tbx5 regulate limb outgrowth and identity , 1999, Nature.
[168] F. Lemonnier,et al. Single H2Kb, H2Db and double H2KbDb knockout mice: peripheral CD8+ T cell repertoire and antilymphocytic choriomeningitis virus cytolytic responses , 1999, European journal of immunology.
[169] C. Tabin,et al. Role of Pitx1 upstream of Tbx4 in specification of hindlimb identity. , 1999, Science.
[170] J. Conboy,et al. Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities. , 1999, The Journal of clinical investigation.
[171] E. Fuchs,et al. FGF-7 modulates ureteric bud growth and nephron number in the developing kidney. , 1999, Development.
[172] A. Satoskar,et al. Targeted Disruption of Migration Inhibitory Factor Gene Reveals Its Critical Role in Sepsis , 1999, The Journal of experimental medicine.
[173] P. Braghetta,et al. Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy. , 1998, Human molecular genetics.
[174] M. Azim Surani,et al. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest , 1998, Nature Genetics.
[175] D. Wagner,et al. Expression of a gene trap reporter construct in a subset of cells in embryonic sites of hematopoiesis: evidence for alternative rRNA production in hematopoietic cells. , 1998, Biochemical and biophysical research communications.
[176] D. Witte,et al. Targeted disruption of the mouse lysosomal acid lipase gene: long-term survival with massive cholesteryl ester and triglyceride storage. , 1998, Human molecular genetics.
[177] C. Tabin,et al. Differential regulation of T-box and homeobox transcription factors suggests roles in controlling chick limb-type identity. , 1998, Development.
[178] D. Roopenian,et al. Maternal IL-11Ralpha function is required for normal decidua and fetoplacental development in mice. , 1998, Genes & development.
[179] L. Silver,et al. Involvement of T-box genes Tbx2-Tbx5 in vertebrate limb specification and development. , 1998, Development.
[180] A. Kasarskis,et al. A phenotype-based screen for embryonic lethal mutations in the mouse. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[181] Pier Paolo Pandolfi,et al. Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies , 1998, Nature Genetics.
[182] R. Schreiber,et al. Disruption of the Jak1 Gene Demonstrates Obligatory and Nonredundant Roles of the Jaks in Cytokine-Induced Biologic Responses , 1998, Cell.
[183] A. Baldini,et al. Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome , 1998, Nature Genetics.
[184] Susan D. Spencer,et al. The Orphan Receptor CRF2-4 Is an Essential Subunit of the Interleukin 10 Receptor , 1998, The Journal of experimental medicine.
[185] H. Lassmann,et al. Targeted inactivation of plectin reveals essential function in maintaining the integrity of skin, muscle, and heart cytoarchitecture. , 1997, Genes & development.
[186] Ueli Schibler,et al. The DBP gene is expressed according to a circadian rhythm in the suprachiasmatic nucleus and influences circadian behavior , 1997, The EMBO journal.
[187] R. Hammer,et al. Elevated levels of SREBP-2 and cholesterol synthesis in livers of mice homozygous for a targeted disruption of the SREBP-1 gene. , 1997, The Journal of clinical investigation.
[188] C. Tabin,et al. Molecular Models for Vertebrate Limb Development , 1997, Cell.
[189] P. Swiatek,et al. IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa , 1997, Mammalian Genome.
[190] S. Narumiya,et al. Failure of parturition in mice lacking the prostaglandin F receptor. , 1997, Science.
[191] J. Sanes,et al. Failure of postsynaptic specialization to develop at neuromuscular junctions of rapsyn-deficient mice , 1995, Nature.
[192] R. Kucherlapati,et al. Mice develop normally without the H1(0) linker histone. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[193] E. Ginns,et al. Metaxin, a gene contiguous to both thrombospondin 3 and glucocerebrosidase, is required for embryonic development in the mouse: implications for Gaucher disease. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[194] E. Olson,et al. Myogenin is required for late but not early aspects of myogenesis during mouse development , 1995, The Journal of cell biology.
[195] R. Hammer,et al. Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons , 1994, Cell.
[196] H. Ozawa,et al. A novel hypothyroid 'growth-retarded' mouse derived from Snell's dwarf mouse. , 1994, The Journal of endocrinology.
[197] S. Suzuki,et al. Enhanced expression of fibronectin by cmd/cmd chondrocytes and its modulation by exogenously added proteoglycan. , 1991, Journal of cell science.
[198] G. Bolelli,et al. The ultradian pulsatile release of gonadotropins in normal female subjects. , 1979, Acta Europaea fertilitatis.
[199] M. Waters,et al. In vivo targeting of the growth hormone receptor (GHR) Box1 sequence demonstrates that the GHR does not signal exclusively through JAK2. , 2010, Molecular endocrinology.
[200] J. Guénet,et al. Gtl2lacZ, an insertional mutation on mouse Chromosome 12 with parental origin-dependent phenotype , 2009, Mammalian Genome.
[201] 木下 将樹. The novel protein kinase Vlk is essential for stromal function of mesenchymal cells , 2009 .
[202] C. S. Raymond,et al. PDGF signaling specificity is mediated through multiple immediate early genes , 2007, Nature Genetics.
[203] S. Shinton,et al. Ablation of ribosomal protein L22 selectively impairs alphabeta T cell development by activation of a p53-dependent checkpoint. , 2007, Immunity.
[204] S. Dimauro,et al. Caveolin-1(-/-)- and caveolin-2(-/-)-deficient mice both display numerous skeletal muscle abnormalities, with tubular aggregate formation. , 2007, The American journal of pathology.
[205] A. Gow,et al. Loss of alpha-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemia. , 2004, The Journal of clinical investigation.
[206] R. Flavell,et al. A crucial role of caspase-3 in osteogenic differentiation of bone marrow stromal stem cells. , 2004, The Journal of clinical investigation.
[207] K. Nasmyth,et al. Loss of the anaphase-promoting complex in quiescent cells causes unscheduled hepatocyte proliferation. , 2004, Genes & development.
[208] D. Russell,et al. Unexpected virilization in male mice lacking steroid 5 alpha-reductase enzymes. , 2001, Endocrinology.
[209] K. Choo,et al. Uterine dysfunction and genetic modifiers in centromere protein B-deficient mice. , 2000, Genome research.
[210] B. Daneholt,et al. The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility. , 2000, Molecular cell.
[211] Y. Barde,et al. The zinc finger protein NRIF interacts with the neurotrophin receptor p75(NTR) and participates in programmed cell death. , 1999, The EMBO journal.
[212] R. Gross,et al. Genetic alteration of phospholipase C beta3 expression modulates behavioral and cellular responses to mu opioids. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[213] T. Hewett,et al. Molecular and physiological effects of alpha-tropomyosin ablation in the mouse. , 1998, Circulation research.
[214] R. Pedersen,et al. Integrin alpha8beta1 is critically important for epithelial-mesenchymal interactions during kidney morphogenesis. , 1997, Cell.
[215] Y. Benjamini,et al. Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .
[216] S. Bryant,et al. A staging system for mouse limb development. , 1989, The Journal of experimental zoology.