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Research 301–330 of 1000+
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Hypotrichosis with juvenile macular dystrophy
- Papular atrichia
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- Primary and Secondary Disturbances in Trace Element Metabolism Connected with Genetic Metabolic Disorders
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Trichothiodystrophy -A Case Report-
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- The <i>IRE</i> gene encodes a protein kinase homologue and modulates root hair growth in <i>Arabidopsis</i>
- Perspectives of Kennedy's disease
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Werner′s syndrome
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- An unusual presentation of X-linked adrenoleukodystrophy
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia