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Research 451–480 of 1000+
- Autotaxin-LPA signaling contributes to obesity-induced insulin resistance in muscle and impairs mitochondrial metabolism
- Identification of hair shaft progenitors that create a niche for hair pigmentation
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Skin inflammation activates intestinal stromal fibroblasts and promotes colitis
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Sarcoidosis: Are there differences in your skin of color patients?
- Effects of lifelong testosterone exposure on health and disease using Mendelian randomization
- Normal Pubertal Development in Daughters of Women With PCOS: A Controlled Study
- Predicting hair cortisol levels with hair pigmentation genes: a possible hair pigmentation bias
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Sebaceous immunobiology - skin homeostasis, pathophysiology, coordination of innate immunity and inflammatory response and disease associations
- Multiomics-empowered Deep Phenotyping of Ulcerative Colitis Identifies Biomarker Signatures Reporting Functional Remission States
- Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer
- Research Relevant Conditions and Pathology in Nonhuman Primates
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Direct cellular reprogramming enables development of viral T antigen–driven Merkel cell carcinoma in mice
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- Exploring the overlap between alopecia areata and major depressive disorder: Epidemiological and genetic perspectives
- Pica for Uncooked Basmati Rice in Two Women with Iron Deficiency and a Review of Ryzophagia
- CD44 signaling in skin wound healing and regeneration
- Lgr6+ stem cells and their progeny in mouse epidermis under regimens of exogenous skin carcinogenesis, and their absence in ensuing skin tumors
- Phosphatase Regulator NIPP1 Restrains Chemokine-Driven Skin Inflammation
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Sphingolipid metabolism orchestrates establishment of the hair follicle stem cell compartment