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Research 361–390 of 1000+
- Assessment of prognostic markers of alopecia areata in pediatric patients
- Dermatologic care of patients with differences of sex development
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Allergic Dermatitis in Pêga Breed Donkeys (Equus asinus) Caused by Culicoides Bites in the Amazon Biome, Pará, Brazil
- Understanding the Secular Decline in Testosterone: Mechanisms, Consequences, and Clinical Perspectives
- Free Testosterone Levels in Patients with Covid-19 and its Association with Disease Severity
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Molecular basis of androgen insensitivity
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Terrestrial vertebrates have two keratin gene clusters; striking differences in teleost fish
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Transcriptome Profiling of Human Follicle Dermal Papilla Cells in response to Porphyra-334 Treatment by RNA-Seq