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Research 61–90 of 1000+
- Mapping cell dynamics in human ex vivo hair follicles suggests pulling mechanism of hair growth
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Clinical-Exome Sequencing Unveils the Genetic Landscape of Polycystic Ovarian Syndrome (PCOS) Focusing on Lean and Obese Phenotypes: Implications for Cost-Effective Diagnosis and Personalized Treatment
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- Biology and Genetics of Hair
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- The hair shaft: normality, abnormality, and genetics
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Anti-androgenic potential of the fruit extracts of certain Egyptian <i>Sabal</i> species and their genetic variability studies: a metabolomic-molecular modeling approach
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Male-pattern baldness susceptibility locus at 20p11
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Inherited Epidermolysis Bullosa: A Clinical Case
- Multiscale spatial mapping of cell populations across anatomical sites in healthy human skin and basal cell carcinoma
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- An Overview of Alopecias
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Genetic Control/Involvement in Hair Fiber Traits
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Genetic Basis of Alopecia Areata
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Emerging concepts about prenatal genesis, aberrant metabolism and treatment paradigms in polycystic ovary syndrome
- Distinct stem cells contribute to mammary gland development and maintenance
- The Rotterdam Study: 2016 objectives and design update