Search
for
Sort by
Research 211–240 of 1000+
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Hair regrowth in a male patient with extensive androgenetic alopecia on estrogen therapy
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Abstracts
- 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
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- 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
- 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
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Genetic basis of polycystic ovary syndrome
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Oral Presentations
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- Genetic prediction of male pattern baldness
- Nuclear Topology, Epigenetics, and Keratinocyte Differentiation
- Diagnostic approach to low‐renin hypertension
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- 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