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Research 511–540 of 1000+
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Pathways to inflammation: acne pathophysiology
- Inherited Disorders of the Hair
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Congenital atrichia and hypotrichosis
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Polycystic ovary syndrome
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Diagnostic approach to low‐renin hypertension
- Nonclassic adrenal hyperplasia
- Animal Models and the Developmental Origins of Polycystic Ovary Syndrome: Increasing Evidence for the Role of Androgens in Programming Reproductive and Metabolic Dysfunction
- Elucidating the roles of three β-glucuronosyltransferases (GLCATs) acting on arabinogalactan-proteins using a CRISPR-Cas9 multiplexing approach in Arabidopsis
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Association between genetically predicted rheumatoid arthritis and alopecia areata: a two-sample Mendelian randomization study
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- Woolly Antics between the Sheaths
- Hair loss in children.
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Androgen receptor gene polymorphism and biological age markers in men
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- 1379 Cell of origin contributes to the melanoma diversity
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Hair and nail involvement in lupus erythematosus
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis