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Research 871–900 of 1000+
- LB1672 Senescent melanocytes in nevus skin stimulate hair growth
- Expression and tissue distribution analysis of vimentin and transthyretin proteins associated with coat colors in sheep (Ovis aries)
- A Bio‐Functional Wnt3a Gradient Microarray for Cell Niche Studies
- 1349 Inducing fate changes at the hair follicle stem cell nice
- 305 Overlaps between inflammatory dermatoses and ichthyoses: need for novel therapeutic approaches
- 581 Spontaneous, Intrinsic Aging in Organ-Cultured Human Skin as Novel Ex Vivo Assay to Test Candidate Anti-Aging Actives
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- Rancangan televisyen: Menyangga atau menyanggah bahasa dan budaya?
- Cellular Senescence: Ageing and Androgenetic Alopecia
- Major Improvement in Wound Healing Through Pharmacologic Mobilization of Stem Cells in Severely Diabetic Rats
- 1250 Development of an ex vivo human skin explant model to examine candidate gene functions in the hair follicle and epidermis
- Pathology of Mouse Models of Accelerated Aging
- Homozygous K5Cre transgenic mice have wavy hair and accelerated malignant progression in a murine model of skin carcinogenesis
- Polycystic Ovary Syndrome
- Basal cell carcinomas in mice arise from hair follicle stem cells and multiple epithelial progenitor populations
- COVID-19 and endocrine and metabolic diseases. An updated statement from the European Society of Endocrinology
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Observation of phenotypic variation among Indian women with polycystic ovary syndrome (PCOS) from Delhi and Srinagar
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Mendelian Randomization Identifies CD25+ CD4+ Tregs and Plasma Proteins in Androgenetic Alopecia Pathogenesis
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- POLİKİSTİK OVER SENDROMU FENOTİPLERİ VE METABOLİK DİSFONKSİYON İLİŞKİSİ
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Activity evaluation of epidermo-melanin unit and dermal damage in melasma
- Electrophoretic variability in human hair: Comparative sodium dodecyl sulfate‐polyacrylamide gel electrophoresis of body and head hair proteins
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Influence of Immune Cells and Circulating Inflammatory Cytokines on Pathological Scars: A Mendelian Randomization Study