Mouse models of human disease. Part I: techniques and resources for genetic analysis in mice

An allelic series of mutations in the kit ligand gene of mice. I. Identification of point mutations in seven ethylnitrosourea-induced Kitl(Steel) alleles.

Genetics·2002

An allelic series of mutations in the Kit ligand gene of mice. II. Effects of ethylnitrosourea-induced Kitl point mutations on survival and peripheral blood cells of Kitl(Steel) mice.

Genetics·2002

Molecular cloning and biological characterization of a novel murine lymphoid growth factor.

The Journal of experimental medicine·2000

Genomic organization, chromosomal localization, tissue distribution, and biophysical characterization of a novel mammalian Shaker-related voltage-gated potassium channel, Kv1.7.

The Journal of biological chemistry·1998

cDNA cloning, expression, subcellular localization, and chromosomal assignment of mammalian aurora homologues, aurora-related kinase (ARK) 1 and 2.

Biochemical and biophysical research communications·1998

Cloning and characterization of a novel class II phosphoinositide 3-kinase containing C2 domain.

Biochemical and biophysical research communications·1998

MCM10 and RECQL4 have cooperative and redundant roles in activating the CMG helicase during the replication initiation.

Genes & development·2026

Decoding anterior-posterior patterning cues into embryo-wide binary fate decisions through recruitment-mediated targeting.

Genes & development·2026

Architectural logic of the 3D genome: mechanisms of dysregulation and emerging cancer therapeutics.

Genes & development·2026

MEIOSIN retains a STRA8-independent activity that contributes to meiotic gene activation across vertebrates.

Genes & development·2026

Maternal small RNAs as gatekeepers of hybrid compatibility in plants and animals.

Genes & development·2026

Chromosomal requirements for formation of multivalent human nucleoli.

Genes & development·2026

Genetic variant profile in a cohort of inherited bone marrow failure patients from North india.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion·2026

Appreciating diversity: a review of the Iranian genomic landscape.

European journal of human genetics : EJHG·2026

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Medicine·2026

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

Stem cell research·2026

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

CNS neuroscience & therapeutics·2026

Related Experiment Videos

Mouse models of human disease. Part I: techniques and resources for genetic analysis in mice

Related Concept Videos

An allelic series of mutations in the kit ligand gene of mice. I. Identification of point mutations in seven ethylnitrosourea-induced Kitl(Steel) alleles.

An allelic series of mutations in the Kit ligand gene of mice. II. Effects of ethylnitrosourea-induced Kitl point mutations on survival and peripheral blood cells of Kitl(Steel) mice.

Molecular cloning and biological characterization of a novel murine lymphoid growth factor.

Genomic organization, chromosomal localization, tissue distribution, and biophysical characterization of a novel mammalian Shaker-related voltage-gated potassium channel, Kv1.7.

cDNA cloning, expression, subcellular localization, and chromosomal assignment of mammalian aurora homologues, aurora-related kinase (ARK) 1 and 2.

Cloning and characterization of a novel class II phosphoinositide 3-kinase containing C2 domain.

MCM10 and RECQL4 have cooperative and redundant roles in activating the CMG helicase during the replication initiation.

Decoding anterior-posterior patterning cues into embryo-wide binary fate decisions through recruitment-mediated targeting.

Architectural logic of the 3D genome: mechanisms of dysregulation and emerging cancer therapeutics.

MEIOSIN retains a STRA8-independent activity that contributes to meiotic gene activation across vertebrates.

Maternal small RNAs as gatekeepers of hybrid compatibility in plants and animals.

Chromosomal requirements for formation of multivalent human nucleoli.

Genetic variant profile in a cohort of inherited bone marrow failure patients from North india.

Appreciating diversity: a review of the Iranian genomic landscape.

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

Related Experiment Videos

Mouse models of human disease. Part I: techniques and resources for genetic analysis in mice

Related Concept Videos

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