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Research 91–120 of 1000+
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- The Impact of Vitamin D Receptor Gene Polymorphisms (FokI, ApaI, TaqI) in Correlation with Oxidative Stress and Hormonal and Dermatologic Manifestations in Polycystic Ovary Syndrome
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors
- Diagnostic approach to low‐renin hypertension
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- The Genetics of Human Skin Disease
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- CRISPR–Cas9: A History of Its Discovery and Ethical Considerations of Its Use in Genome Editing
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Adams–Oliver syndrome: new evidence in variable expressivity?
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Topical minoxidil and tretinoin combined with an oral vitamin D analog as a treatment for woolly hair
- Woolly Hair in Two Siblings
- Androgenetic alopecia: pathogenesis and potential for therapy