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Research 151–180 of 1000+
- Congenital atrichia with papular lesions
- Genetics of Alopecia
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Unexpected Autocrine Role of Vascular Endothelial Growth Factor in Squamous Cell Carcinoma
- KRT16 wt Allele
- SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene on Fibre Traits in Inner Mongolia Cashmere Goats
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- The organization of the keratin I and II gene clusters in placental mammals and marsupials show a striking similarity
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- Seasonal Gene Expression Profile Responsible for Hair Follicle Development in Angora Goats