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Research 541–570 of 1000+
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Extracellular vesicles in age-related diseases: disease pathogenesis, intervention, and biomarker
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia
- Inborn Errors of Biotin Metabolism
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Whole blood transcriptome profiling identifies candidate genes associated with alopecia in male giant pandas (Ailuropoda melanoleuca)
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- 130 Expression of nidogen1 in basal cell carcinoma
- Cyberspace Chat
- FOXN1 deficient nude severe combined immunodeficiency
- Premature aging and cancer development in transgenic mice lacking functional CYLD
- Predicting Human Appearance from DNA for Forensic Investigations
- Pharmacologic interventions in aging hair
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Functional Interpretation of Genome-Wide Association Study Evidence in Alopecia Areata
- The Role of Extracellular Vesicles in Cutaneous Remodeling and Hair Follicle Dynamics
- Genotyping of the rs1800440 Polymorphism in CYP1B1 Gene and the rs9258883 Polymorphism in HLA-B Gene in a Spanish Cohort of 223 Patients with Frontal Fibrosing Alopecia
- JAK-centric explainable few-shot gene-expression diagnosis framework for alopecia via MultiPLIER priors and relation-style set-to-set comparison
- Pathophysiology of Androgenetic Alopecia and Implications for Treatment: An Overview of Current Literature
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek