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Research 61–90 of 1000+
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Alopezien und Hypotrichosen im Kindesalter
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Alopecia totalis in an infant
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- Congenital hair loss disorders: Rare, but not too rare
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Office Diagnosis of Hair Shaft Defects
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Keratin disorders: from gene to therapy
- Regulation of a hair follicle keratin intermediate filament gene promoter
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Research Snippets
- Current Genetics in Hair Diseases
- Early Dengue Virus Infection in Human Skin: A Cycle of Inflammation and Infectivity