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Research 31–60 of 1000+
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis
- Combinatorial expression of cell cycle regulators is more suitable for immortalization than oncogenic methods in dermal papilla cells
- BIPHENOTYPIC LEUKAEMIA
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Androgen receptors and their biology
- Depression from a physical symptom.
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Molecular basis of androgen insensitivity
- Male fertility and skin diseases
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- This Month in the Journal
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Clinical relevance of hair microscopy in alopecia
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles