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Research 961–990 of 1000+
- 308 Epidermal keratinocytes regulate bacterial immune responses and host defense through EGFR
- Characterization of an autoimmune condition associated with AEC syndrome
- A single type of progenitor cell maintains normal epidermis
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Enhanced ectodysplasin-A receptor (EDAR) signaling alters multiple fiber characteristics to produce the East Asian hair form
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- A Pharmacogenetic Survey of Androgen Receptor (CAG)N and (GGN)N Polymorphisms in Patients Experiencing Long Term Side Effects after Finasteride Discontinuation
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Phenotypic, transcriptomic, and genomic analyses reveal the spatiotemporal patterns and associated genes of coarse hair density in goats
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- Generation of a Novel Inducible and Dermal Papilla‐Specific <i>Wif1‐CreER</i> Knock‐In Mouse Line for Hair Follicle Research
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- 1301 STIM1, but not STIM2, is the calcium sensor critical for sweat secretion
- The role of functional variants in the aetiology of polycystic ovary syndrome
- Review of the Literature
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases