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Research 931–960 of 1000+
- Epigenetics of Colorectal Cancer
- Dermal papilla cell number specifies hair size, shape and cycling and its reduction causes follicular decline
- Role of insulin, insulin‐like growth factor‐1, hyperglycaemic food and milk consumption in the pathogenesis of acne vulgaris
- FGF5 is a crucial regulator of hair length in humans
- Genetically Altered Expression of Spermidine/Spermine N1-Acetyltransferase Affects Fat Metabolism in Mice via Acetyl-CoA
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Frizzled Receptors in Development and Disease
- The structure and organization of lanceolate mechanosensory complexes at mouse hair follicles
- Epidermal Vascular Endothelial Growth Factor Production Is Required for Permeability Barrier Homeostasis, Dermal Angiogenesis, and the Development of Epidermal Hyperplasia
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Molecular mechanisms of asymmetric divisions in mammary stem cells
- Role of the Notch Ligand Delta1 in Embryonic and Adult Mouse Epidermis
- SHISA6 Confers Resistance to Differentiation-Promoting Wnt/β-Catenin Signaling in Mouse Spermatogenic Stem Cells
- Vitiligo and alopecia areata: apples and oranges?
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- New clinico‐genetic classification of trichothiodystrophy
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration
- Extra-Intestinal Manifestation of Celiac Disease in Children
- Methotrexate for induction of remission in ulcerative colitis
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Characteristics of Androgenetic Alopecia in Asian
- Vitamin D Receptor, UVR, and Skin Cancer: A Potential Protective Mechanism
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA