Search
for
Sort by
Research 211–240 of 1000+
- Pharmacogenetic analysis of human steroid 5α reductase type II: comparison of finasteride and dutasteride
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- What does acne genetics teach us about disease pathogenesis?
- Genetic basis of polycystic ovary syndrome
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- New Horizons in the Genetics of Polycystic Ovary Syndrome: From Predisposition to Precision Medicine.
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- 236 Wnt/planar cell polarity impairment and the genetics of yellow nail syndrome
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Fetal Programming of Polycystic Ovary Syndrome by Androgen Excess: Evidence from Experimental, Clinical, and Genetic Association Studies
- Enanthem in Patients With COVID-19 and Skin Rash
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- Recently Identified Forms of Epidermolysis Bullosa
- Common variants in the sex hormone-binding globulin gene (SHBG) and polycystic ovary syndrome (PCOS) in Mediterranean women
- Genetic association of <i>HLA‐DQB1</i> and <i>HLA‐DRB1</i> polymorphisms with alopecia areata in the Italian population
- Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Panfolliculoma: Report of the Youngest Case and Literature Review of Its Histopathologic Variants
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis