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Research 361–390 of 1000+
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Treatment of alopecia areata: “What is new on the horizon?”
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Bloom's syndrome–‐a first report from India
- Potential Role of the Epidermal Differentiation Complex in the Pathogenesis of Psoriasis
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Atrichia with papular lesions
- Disease causing homozygous variants in the human hairless gene
- Pigmentary mosaicism: An update
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Combinatorial expression of cell cycle regulators is more suitable for immortalization than oncogenic methods in dermal papilla cells
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Congenital atrichia with papular lesions
- Marie-unna hereditary hypotrichosis
- Monilethrix
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Case Report: Disorder of Sexual Development in a Chinese Crested Dog With XX/XY Leukocyte Chimerism and Mixed Cell Testicular Tumors