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Research 91–120 of 1000+
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Potential Role of the Epidermal Differentiation Complex in the Pathogenesis of Psoriasis
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- The hair shaft: normality, abnormality, and genetics
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Atrichia with papular lesions
- Disease causing homozygous variants in the human hairless gene
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- Expression of novel keratin associated protein 5 genes in the cuticle layer of human hair follicles
- Combinatorial expression of cell cycle regulators is more suitable for immortalization than oncogenic methods in dermal papilla cells
- Marie-unna hereditary hypotrichosis
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Familial congenital generalized hypertrichosis
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Monilethrix: Beaded hair and hypotrichosis in a child
- Congenital Atrichia: A Case Report
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Papular atrichia
- A review of genetic researches of and rogenic alopecia
- ANDROGENIC ALOPECIA: PATHOGENETIC MECHANISMS AND THERAPEUTIC APPROACHES
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Molecular genetics of androgen insensitivity
- Alopecia areata and Down syndrome: A true association and the importance of dermoscopic diagnosis
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse