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Research 30
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Biology and Genetics of Hair
- Molecular Genetics of Alopecias
- Keratin disorders: from gene to therapy
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Congenital hair loss disorders: Rare, but not too rare
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Current Genetics in Hair Diseases
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Effect of Oral Minoxidil on Monilethrix
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Inherited Disorders of the Hair
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- The human keratins: biology and pathology
- The molecular basis of human keratin disorders
- Neuroendocrine Controls of Keratin Expression in Human Skin