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Research 181–210 of 1000+
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Is polycystic ovary syndrome a sexual conflict? A review
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Identification of the key proteins associated with different hair types in sheep and goats
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- The Genetics of Human Skin Disease
- A bibliometric study of scientific literature in Scopus on botanicals for treatment of androgenetic alopecia
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Developmental Mechanisms Controlling Cell Fate, Evolution of
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Hair Coloration by Gene Regulation: Fact or Fiction?
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- Both low circulating insulin-like growth factor-1 and high-density lipoprotein cholesterol are associated with hair loss in middle-aged women
- Skin transcriptome reveals the Periodic changes in genes underlying hair follicle cycling in Cashmere goats
- Updates from the British Association of Dermatologists 91st Annual Meeting, 5-7 July 2011, London, U.K.
- Defining the identity of mouse embryonic dermal fibroblasts
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes