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Research 241–270 of 1000+
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- 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
- Transcriptome Dynamics Reveal Stage-Specific and Melatonin-Triggered Gene Expression Patterns During The Cashmere Growth Cycle in Capra Hircus
- General Dermatology
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Editors' Picks
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Sjogren-Larsson syndrome
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- LAMELLAR ICHTHYOSIS: ONE CASE REPORT
- Epidemiological and investigative study of premature graying of hair in higher secondary and pre-university school children
- Delving into diversity: exploring different risk factors of premature greying of hair
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- Skin features in myotonic dystrophy type 1: An observational study
- Alopecia: Association with Resistance to Thyroid Hormones