Search
for
Sort by
Research 241–270 of 1000+
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- No improvement in male-pattern hair loss using laser hair-comb therapy: a 6-month, half-head, assessor-blinded investigation in two men
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Abstracts
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Association Between Insulin Resistance and Hyperandrogenism in Women with PCOS. A Cross-Sectional Clinical Study
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- 5-Alpha-Reductase Inhibitors and Combination Therapy
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- 316 Specialized ribosomes in human dermal fibroblast senescence
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- SLE and Serum Complement: Causative, Concomitant or Coincidental?
- Evidence of a Causal Relationship Between Body Mass Index and Immune-Mediated and Inflammatory Skin Diseases and Biomarkers: A Mendelian Randomization Study
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- Keratin disorders: from gene to therapy
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- Congenital adrenal hyperplasia
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Congenital hair loss disorders: Rare, but not too rare
- Diagnostic approach to low‐renin hypertension
- Genetic basis of polycystic ovary syndrome
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient