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Research 751–780 of 1000+
- Do Changes in Chromosomes Cause Aging?
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Optimal Management of Hair Loss (Alopecia) in Children
- Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
- Association between the D19S884 marker at the insulin receptor gene locus and polycystic ovary syndrome
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Inherited ichthyosis: Syndromic forms
- Hair follicle and interfollicular epidermal stem cells make varying contributions to wound regeneration
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- The biology of hair diversity
- Module-based complexity formation: periodic patterning in feathers and hairs
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Defects in Androgen Biosynthesis Causing 46,XY Disorders of Sexual Development
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Poliosis circumscripta: Overview and underlying causes
- Cicatricial (Scarring) Alopecias
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Drug repositioning: current approaches and their implications in the precision medicine era
- Identification of the Ovine Keratin-Associated Protein 22-1 (KAP22-1) Gene and Its Effect on Wool Traits
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Congenital hair loss disorders: Rare, but not too rare
- Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis
- <i>NUDT15</i>,<i>FTO</i>, and<i>RUNX1</i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases
- Pubertal Development