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Research 301–330 of 1000+
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Chi-miR-130b-3p regulates Inner Mongolia cashmere goat skin hair follicles in fetuses by targeting<i>Wnt family member 10A</i>
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Genetic analysis of a novel antioxidant multi-target iron chelator, M30 protecting against chemotherapy-induced alopecia in mice
- Examination of epigenetic inhibitor zebularine in treatment of skin wounds in healthy and diabetic mice
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Mechanism of Apoptotic Regulation of Follicular Regression
- Current Genetics in Hair Diseases
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- George Ernest Rogers 1927–2021
- Comparative transcriptome profiling of hair follicles from forest musk deer (Moschus berezovskii) at different stages
- Parental uveitis causes elevated hair loss in offspring of C57BL/6J mice
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- The population dynamics of cancer: a Darwinian perspective
- MicroRNAs in skin tissue engineering
- The Aromatase Inhibitor Fadrozole and the 5-Reductase Inhibitor Finasteride Affect Gonadal Differentiation and Gene Expression in the Frog <i>Silurana tropicalis</i>
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Dermal niche signaling and epidermal stem cells
- Editors' Picks
- Single-Cell Transcriptomic Identification of a Proliferative Intermediate State During Early Anagen Hair Follicle Regeneration
- miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- Transcriptome Reveals Long Non-coding RNAs and mRNAs Involved in Primary Wool Follicle Induction in Carpet Sheep Fetal Skin