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Research 61–90 of 1000+
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Diagnostic approach to low‐renin hypertension
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Molecular genetics of androgen insensitivity
- Idiopathic Hirsutism*
- The Changing Landscape of Alopecia Areata: The Translational Landscape
- TMPRSS2: A Key Host Factor in SARS-CoV-2 Infection and Potential Therapeutic Target
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- THE PATHOGENESIS OF ALOPECIA AREATA
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- ANDROGENIC ALOPECIA: PATHOGENETIC MECHANISMS AND THERAPEUTIC APPROACHES
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Pilot study: genetic distribution of AR, FGF5, SULT1A1 and CYP3A5 polymorphisms in male Mexican population with androgenetic alopecia.