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Research 421–450 of 1000+
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- 773 Generation of human hair follicle organoids in vitro and ex vivo by co-culture of primary human hair matrix keratinocytes and dermal papilla fibroblasts
- 837 From genotoxic stresses to skin damage: Distinct, novel mechanisms of skin and hair damage in chemo/radiation therapy
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS)
- Towards a molecular understanding of hair loss and its treatment
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- An Update of Congenital Adrenal Hyperplasia
- Principles of Hair Cycle Control
- Androgens and androgen receptor action in skin and hair follicles
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Diagnostic approach to low‐renin hypertension
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Development of Autoimmune Hair Loss Disease Alopecia Areata Is Associated with Cardiac Dysfunction in C3H/HeJ Mice
- Genetic basis of polycystic ovary syndrome
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Biotinidase deficiency characterized by skin and hair findings
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- Epigenetic regulations on skin wound healing: implications from current researches.
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Comprehensive transcriptome profiling between balding and non-balding scalp of female pattern hair loss in Asian
- Congenital Atrichia: A Case Report
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- An immune regulatory CCT repeat containing oligodeoxynucleotide capable of causing hair loss in male mice
- 9. Immunology and Genetics
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor