| scholarly article | Q13442814 |
| P50 | author | Olga Ermakova | Q56815097 |
| Dominika Farley | Q57442510 | ||
| Tiago Ferreira | Q58203887 | ||
| Claus Nerlov | Q87969398 | ||
| Lukasz Piszczek | Q91018330 | ||
| Richard Moriggl | Q38327183 | ||
| Rosa Chiara Paolicelli | Q42865567 | ||
| P2093 | author name string | Luisa Luciani | |
| Stefania Rizzo | |||
| Nicholas M Luscombe | |||
| Cornelius Gross | |||
| Florence M G Cavalli | |||
| Mumna Al-Banchaabouchi | |||
| P2860 | cites work | Bioconductor: open software development for computational biology and bioinformatics | Q21194861 |
| The knockout mouse project | Q22122054 | ||
| Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease | Q22251069 | ||
| Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease | Q24306416 | ||
| Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice | Q24602261 | ||
| The European dimension for the mouse genome mutagenesis program | Q24644441 | ||
| Efficient gene-driven germ-line point mutagenesis of C57BL/6J mice | Q25255702 | ||
| Parallel phenotypic analysis of sporulation and postgermination growth in Saccharomyces cerevisiae | Q27931084 | ||
| STAT3 mutations in the hyper-IgE syndrome | Q28249785 | ||
| Stat5 activation is uniquely associated with cytokine signaling in peripheral T cells | Q28511057 | ||
| TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome | Q28512803 | ||
| The Min (multiple intestinal neoplasia) mutation: its effect on gut epithelial cell differentiation and interaction with a modifier system | Q28513603 | ||
| A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy | Q28590547 | ||
| The HapMap and genome-wide association studies in diagnosis and therapy | Q28752130 | ||
| affy--analysis of Affymetrix GeneChip data at the probe level | Q29547353 | ||
| Systematic screen for human disease genes in yeast | Q29617873 | ||
| Differential involvement of the central amygdala in appetitive versus aversive learning | Q30500479 | ||
| Mutagenic insertion and chromosome engineering resource (MICER). | Q33204468 | ||
| Gene expression signature of cerebellar hypoplasia in a mouse model of Down syndrome during postnatal development | Q33424071 | ||
| A comparison of wild-caught wood mice and bank voles in the Intellicage: assessing exploration, daily activity patterns and place learning paradigms | Q33448717 | ||
| Structural variation in the human genome and its role in disease | Q33522758 | ||
| Clarifying the role of Stat5 in lymphoid development and Abelson-induced transformation | Q33874580 | ||
| Functional annotation of mammalian genomic DNA sequence by chemical mutagenesis: a fine-structure genetic mutation map of a 1- to 2-cM segment of mouse chromosome 7 corresponding to human chromosome 11p14-p15. | Q33894561 | ||
| Developmental exposure to methylmercury alters learning and induces depression-like behavior in male mice | Q48318644 | ||
| Segmental copy number variation shapes tissue transcriptomes | Q48712677 | ||
| Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. 1979. | Q49012176 | ||
| Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes. | Q50313568 | ||
| Inversion-induced disruption of the Hoxd cluster leads to the partition of regulatory landscapes. | Q52565016 | ||
| Severe growth hormone insensitivity resulting from total absence of signal transducer and activator of transcription 5b. | Q53623601 | ||
| EMPReSS: standardized phenotype screens for functional annotation of the mouse genome. | Q55041356 | ||
| Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome | Q57812915 | ||
| Engineering chromosomes in mice through targeted meiotic recombination (TAMERE) | Q59986797 | ||
| Allelic phasing of a mouse chromosome 11 deficiency influences p53 tumorigenicity | Q73425426 | ||
| A new candidate site for a tumor suppressor gene involved in mouse thymic lymphomagenesis is located on the distal part of chromosome 4 | Q77436448 | ||
| Growth hormone insensitivity associated with a STAT5b mutation | Q78758749 | ||
| STAT5 activity in pancreatic beta-cells influences the severity of diabetes in animal models of type 1 and 2 diabetes | Q79143532 | ||
| Multiple trait measurements in 43 inbred mouse strains capture the phenotypic diversity characteristic of human populations | Q79819519 | ||
| Cutting edge: An in vivo requirement for STAT3 signaling in TH17 development and TH17-dependent autoimmunity | Q81317182 | ||
| Genetic variants in STAT3 are associated with nonalcoholic fatty liver disease | Q81961747 | ||
| Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease). | Q33910305 | ||
| Reduced number of hypocretin neurons in human narcolepsy | Q33923479 | ||
| Essential role of STAT3 in the control of the acute-phase response as revealed by inducible gene inactivation [correction of activation] in the liver | Q33967216 | ||
| Segmental aneuploidy and the genetic gross structure of the Drosophila genome | Q33988128 | ||
| Diet-induced atherosclerosis in mice heterozygous and homozygous for apolipoprotein E gene disruption | Q34181941 | ||
| Transgenic mice expressing high levels of human apolipoprotein B develop severe atherosclerotic lesions in response to a high-fat diet. | Q34218397 | ||
| Stat5a/b are essential for normal lymphoid development and differentiation | Q34253065 | ||
| Chromosome engineering in mice | Q34290413 | ||
| Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse | Q34344768 | ||
| Embryonic lethality and tumorigenesis caused by segmental aneuploidy on mouse chromosome 11. | Q34605754 | ||
| Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability | Q34652997 | ||
| EUCOMM--the European conditional mouse mutagenesis program. | Q34707596 | ||
| Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome | Q34777768 | ||
| CD4 T cells: fates, functions, and faults | Q34813153 | ||
| Mouse models of genomic syndromes as tools for understanding the basis of complex traits: an example with the smith-magenis and the potocki-lupski syndromes | Q35015379 | ||
| Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome | Q35574036 | ||
| A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse | Q35729853 | ||
| Cytokine signaling modules in inflammatory responses | Q37133450 | ||
| Population analysis of large copy number variants and hotspots of human genetic disease | Q37156109 | ||
| The transcription factors Stat5a/b are not required for islet development but modulate pancreatic beta-cell physiology upon aging | Q37225633 | ||
| NIH experiment in centralized mouse phenotyping: the Vanderbilt experience and recommendations for evaluating glucose homeostasis in the mouse | Q37391778 | ||
| Genetics and the general physician: insights, applications and future challenges | Q37396981 | ||
| CNVs and genetic medicine (excitement and consequences of a rediscovery). | Q37415133 | ||
| A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome | Q37423613 | ||
| Inactivation of Stat5 in mouse mammary epithelium during pregnancy reveals distinct functions in cell proliferation, survival, and differentiation | Q37493064 | ||
| Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome | Q40098119 | ||
| Inhibition of early atherogenesis in transgenic mice by human apolipoprotein AI. | Q41164669 | ||
| Evidence for a cluster of genes on chromosome 17q11-q21 controlling susceptibility to tuberculosis and leprosy in Brazilians | Q42617770 | ||
| Antigen-specific T cell sensitization is impaired in IL-17-deficient mice, causing suppression of allergic cellular and humoral responses | Q44158655 | ||
| Effect of diets on lipoprotein concentrations in heterozygous apolipoprotein E-deficient mice. | Q45180000 | ||
| CD8+ T cells are effector cells of contact dermatitis to common skin allergens in mice. | Q46926239 | ||
| Toward simpler and faster genome-wide mutagenesis in mice | Q48078788 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| limma | Q112236343 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 50-66 | |
| P577 | publication date | 2011-01-01 | |
| P1433 | published in | EMBO Molecular Medicine | Q15817279 |
| P1476 | title | Sensitized phenotypic screening identifies gene dosage sensitive region on chromosome 11 that predisposes to disease in mice | |
| P478 | volume | 3 |
| Q39294873 | Construction and phenotypic analysis of mice carrying a duplication of the major histocompatibility class I (MHC-I) locus. |
| Q42245090 | Copy number variation and susceptibility to complex traits |
| Q34606927 | Enhanced T cell lymphoma in NOD.Stat5b transgenic mice is caused by hyperactivation of Stat5b in CD8+ thymocytes |
| Q92253988 | High activation of STAT5A drives peripheral T-cell lymphoma and leukemia |
| Q55363878 | Mouse models of aneuploidy. |
| Q47375997 | STAT5BN642H is a driver mutation for T cell neoplasia |
| Q42600535 | Serotonin 1A auto-receptors are not sufficient to modulate anxiety in mice |
| Q58455445 | Stat5 gene dosage in T cells modulates CD8+T-cell homeostasis and attenuates contact hypersensitivity response in mice |
| Q47758492 | Wnt/β-Catenin Signaling Induces Integrin α4β1 in T Cells and Promotes a Progressive Neuroinflammatory Disease in Mice. |
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