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Research 301–330 of 1000+
- Genetic Control/Involvement in Hair Fiber Traits
- Genetic and biochemical aspects of the synthesis of keratin by hair follicles
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Progeroide Syndrome
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Association between androgenetic alopecia and cardiovascular diseases: a genetic correlation and Mendelian randomization study
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Genetics
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Molecular Genetics of Human Hair Diseases
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- Alopecia in Epidermolysis Bullosa
- Gene Variant in Amish a Clue to Better Aging
- Role of insulin resistance and diet in acne
- The endocrinology of baldness
- METABOLIC DISOEDEKS AND HAIE GEOWTH
- Anti-Müllerian hormone gene polymorphism is associated with androgen levels in Chinese polycystic ovary syndrome patients with insulin resistance
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Seborrheic Dermatitis as a Potential Trigger of Central Centrifugal Cicatricial Alopecia: A Review of Literature
- Boundary Conditions Cause Different Generic Bifurcation Structures in Turing Systems
- Genome‐wide association study identifies variants associated with hair length in Brangus cattle
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Keratosis follicularis spinulosa decalvans in a female
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Assessment of androgenic hormones and other risk factors in Egyptian males with early onset androgenetic alopecia: a case control study