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Research 391–420 of 1000+
- Congenital adrenal hyperplasia
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Ether: Fiction or Reality? A Review
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Symposium Proceedings of the 4th Intercontinental Meeting of Hair Research Societies: “The World of Hair 2004”
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Biology of Human Hair: Know Your Hair to Control It
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Role of skin enzymes in metabolism of topical drugs
- Induction of dermal fibroblasts into dermal papilla cell-like cells in hydrogel microcapsules for enhanced hair follicle regeneration
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Hashimoto Thyroiditis - A Comprehensive Review
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Equine adipose tissue derived stem cells and their multilineage differentiation
- British Society for Dermatopathology
- Identification of Familial Infections Using Multilocus Microsatellite Typing in Tinea Corporis due to <i>Microsporum canis</i>
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Keratin disorders: from gene to therapy
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene