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Research 61–90 of 1000+
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- 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?”
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Bloom's syndrome–‐a first report from India
- Potential Role of the Epidermal Differentiation Complex in the Pathogenesis of Psoriasis
- 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
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Disease causing homozygous variants in the human hairless gene
- 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
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Frontal Fibrosing Alopecia
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Congenital Atrichia: A Case Report
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- BRITISH ASSOCIATION OF DERMATOLOGY.
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- Homologous recombination induced by doxazosin mesylate and saw palmetto in the <i>Drosophila</i> wing‐spot test