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Research 391–420 of 1000+
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Genetic Basis of Male Pattern Baldness
- Keratin gene mutations in disorders of human skin and its appendages
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Analogs of human genetic skin disease in domesticated animals
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Genetic Hair Disorders: A Review
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Time-course RNA-seq analysis reveals stage-specific and melatonin-triggered gene expression patterns during the hair follicle growth cycle in Capra hircus
- Genetic Control/Involvement in Hair Fiber Traits
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1