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Research 271–300 of 1000+
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- BJD Editor's Choice
- 14. Wound Healing; Cutaneous Therapy; Hair
- Registrars’ Symposium: Summaries of Papers
- Pilot study: genetic distribution of AR, FGF5, SULT1A1 and CYP3A5 polymorphisms in male Mexican population with androgenetic alopecia.
- Study on genetic polymorphisms of androgen receptor gene and 5α-reductase genes of Han men with androgenetic alopecia in the Eastern China
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- Intermittent nitrate transdermal therapy
- MicroRNA control of signal transduction
- <i>Hoxc13</i> mutant mice lack external hair
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan
- Oncogenes and morphogens: intricacies of targeted therapy in cutaneous basal cell carcinoma
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Association of Rs231775 Genetic Variant of Cytotoxic T-lymphocyte Associated Protein 4 with Alopecia Areata Disease in Males: A Case–Control Study
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Standardizing the Nomenclature of Grafts
- Management of a Refractory EIF3E-RSPO2 Fusion Positive Pilomatrical Cancer Patient with Encyclopedic Tumor Analysis Guided Treatment
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Alopecia areata: An update
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Nonclassic adrenal hyperplasia
- Nonclassic Congenital Adrenal Hyperplasia
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Androgen receptor gene polymorphism and polycystic ovary syndrome