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Research 511–540 of 1000+
- Matriptase-2, A Novel Suppressor of Hepcidin.
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Pinkie, the First Viable Germline Hypomorph Allele of Retinoid X Receptor Alpha, Reveals an Important Role for RXRa in Th2 Development.
- Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice
- Brief study of hypertrichosis
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- 547 CDK9 Kinase Activation in Association with AFF1-SEC Initiate Epidermal Progenitor differentiation
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Research Snippets
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- Cleave but not leave: Astrotactin proteins in development and disease
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- IL-17 axis is a significant driver of skin inflammation in Card14 mutant pityriasis rubra pilaris model mice
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Therapeutics for COVID-19 and post COVID-19 complications: An update
- Zinc metabolism in lethal-milk mice
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Exome analysis for Cronkhite-Canada syndrome: A case report
- 545 Skin Organoids derived from NCSTN mutated patient-induced pluripotent stem cells recapitulate Hidradenitis Suppurativa pathogenic hallmarks
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Clinical Snippets
- Genetic characterization of congenital defects in dogs : caudal dysplasia, ectodermal dysplasia and mucopolysaccharidosis VII
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players