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- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Current Genetics in Hair Diseases
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Biology and Genetics of Hair
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Inherited Disorders of the Hair
- Genetics of Structural Hair Disorders
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Biotin
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Analogs of human genetic skin disease in domesticated animals
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hair loss disorders: Rare, but not too rare
- Molecular Genetics of Alopecias
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Keratins: the hair shaft's backbone revealed
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease