Frequencies of human keratin 10 alleles

[Sporotrichosis as the cause of a leg ulcer].

Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete·2003

Identification of human epidermal differentiation complex (EDC)-encoded genes by subtractive hybridization of entire YACs to a gridded keratinocyte cDNA library.

Genome research·2001

Complex RNA processing of TDRKH, a novel gene encoding the putative RNA-binding tudor and KH domains.

Gene·2000

Isolation and characterization of human and mouse ZIRTL, a member of the IRT1 family of transporters, mapping within the epidermal differentiation complex.

Genomics·1999

Genomic organization and mapping of the human and mouse neuronal beta2-nicotinic acetylcholine receptor genes.

Mammalian genome : official journal of the International Mammalian Genome Society·1999

Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy.

American journal of medical genetics·1999

Prevalence and mechanistic origins of genome-wide ploidy abnormalities in ICSI derived human preimplantation embryos.

Human molecular genetics·2026

Myofibrillar myopathy-associated KY protein promotes muscle fibre size rescue independent of its predicted catalytic triad.

Human molecular genetics·2026

In vivo dissection of human NRXN1 isoforms reveals gain-of-function pathogenicity of schizophrenia-associated 3' deletions.

Human molecular genetics·2026

A mouse model of autosomal dominant spastic ataxia and myopathy caused by a mutation in Tuba4a.

Human molecular genetics·2026

BIN1 overexpression rescues cardiac but not skeletal muscle defects in a mouse model of caveolinopathy.

Human molecular genetics·2026

Unlocking the epigenetic code: future Frontiers in predictive biomarkers for intellectual disability in fragile X syndrome.

Human molecular genetics·2026

Association of miR-499, miR-27a, and miR-34a Gene Polymorphisms With Susceptibility to Type 2 Diabetes Mellitus in an Iranian Population: A Case-Control Study.

BioMed research international·2026

Atherosclerotic plaque fibroblasts derive from adventitial and medial Pdgfra-lineage-positive cells and predominantly maintain fibroblast identity.

Cardiovascular research·2026

Revealing Causal Proteomic Signatures of Hypertension: Systematic Insights From Proteome-Wide Mendelian Randomization.

Hypertension (Dallas, Tex. : 1979)·2026

Inheritance entropy: A model-independent method to probe the hereditary structure of cell lineage trees.

PRX life·2026

Early life high-fat diet exposure modulates adult metabolic phenotypes in Drosophila.

iScience·2026

Decoding the Link: Exploring FMO3 Gene Variations as a Key to Understanding Type Two Diabetes Through Bioinformatics and Case-Control Analyses.

Indian journal of clinical biochemistry : IJCB·2026

Related Experiment Videos

Frequencies of human keratin 10 alleles

Related Concept Videos

[Sporotrichosis as the cause of a leg ulcer].

Identification of human epidermal differentiation complex (EDC)-encoded genes by subtractive hybridization of entire YACs to a gridded keratinocyte cDNA library.

Complex RNA processing of TDRKH, a novel gene encoding the putative RNA-binding tudor and KH domains.

Isolation and characterization of human and mouse ZIRTL, a member of the IRT1 family of transporters, mapping within the epidermal differentiation complex.

Genomic organization and mapping of the human and mouse neuronal beta2-nicotinic acetylcholine receptor genes.

Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy.

Prevalence and mechanistic origins of genome-wide ploidy abnormalities in ICSI derived human preimplantation embryos.

Myofibrillar myopathy-associated KY protein promotes muscle fibre size rescue independent of its predicted catalytic triad.

In vivo dissection of human NRXN1 isoforms reveals gain-of-function pathogenicity of schizophrenia-associated 3' deletions.

A mouse model of autosomal dominant spastic ataxia and myopathy caused by a mutation in Tuba4a.

BIN1 overexpression rescues cardiac but not skeletal muscle defects in a mouse model of caveolinopathy.

Unlocking the epigenetic code: future Frontiers in predictive biomarkers for intellectual disability in fragile X syndrome.

Association of miR-499, miR-27a, and miR-34a Gene Polymorphisms With Susceptibility to Type 2 Diabetes Mellitus in an Iranian Population: A Case-Control Study.

Atherosclerotic plaque fibroblasts derive from adventitial and medial Pdgfra-lineage-positive cells and predominantly maintain fibroblast identity.

Revealing Causal Proteomic Signatures of Hypertension: Systematic Insights From Proteome-Wide Mendelian Randomization.

Inheritance entropy: A model-independent method to probe the hereditary structure of cell lineage trees.

Early life high-fat diet exposure modulates adult metabolic phenotypes in Drosophila.

Decoding the Link: Exploring FMO3 Gene Variations as a Key to Understanding Type Two Diabetes Through Bioinformatics and Case-Control Analyses.

Related Experiment Videos

Frequencies of human keratin 10 alleles

Related Concept Videos

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