Search
for
Sort by
Research 661–690 of 1000+
- The Yin–Yang of Stress and Senescence: Integrated Stress Response and SASP Crosstalk in Stem Cell Fate, Regeneration, and Disease
- 0867 The role of schwann cell - macrophage interactions in keloid pathogenesis
- 0952 Spatial transcriptomics reveal compartmentalized dysregulation of lipid metabolism in acne vulgaris
- 685 Modelling intrinsic and extrinsic cellular senescence in vitro with complex bioengineered human skin constructs
- 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
- 1250 Development of an ex vivo human skin explant model to examine candidate gene functions in the hair follicle and epidermis
- 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
- 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
- Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
- COVID-19 and endocrine and metabolic diseases. An updated statement from the European Society of Endocrinology
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- The Frequency of Metabolic Syndrome is Higher Among PCOS Brazilian Women With Menstrual Irregularity Plus Hyperandrogenism
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation
- Inherited Hair Disorders
- Clinical features and presentation of polycystic ovary syndrome
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Basal cell carcinomas in mice arise from hair follicle stem cells and multiple epithelial progenitor populations
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Electrophoretic variability in human hair: Comparative sodium dodecyl sulfate‐polyacrylamide gel electrophoresis of body and head hair proteins