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Research 31–60 of 495
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- How to diagnose a lipodystrophy syndrome
- Female Hirsutism: Pathophysiological Considerations and Therapeutic Implications*
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- Redefining hormone resistance in prostate cancer
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Immune cell regulation of the hair cycle
- Genome-wide association study of skin complex diseases
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Endocrinology and auxology of sibships with non-classical congenital adrenal hyperplasia.
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Darier Sign: A Historical Note
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Inherited Disorders of the Hair
- Acne
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women