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Research 211–240 of 823
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- The hair follicle enigma
- Hair keratin KRT81 is expressed in normal and breast cancer cells and contributes to their invasiveness
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Maternal androgen excess induces cardiac hypertrophy and left ventricular dysfunction in female mice offspring
- Is polycystic ovary syndrome a sexual conflict? A review
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- Genetic basis of polycystic ovary syndrome
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- PCOS: update and diagnostic approach
- The genetics of alopecia areata
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- The influence of obesity on Androstenedione to Testosterone ratio in women with polycystic ovary syndrome (PCOS) and hyperandrogenemia
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- 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
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- Anti-Müllerian hormone gene polymorphism is associated with androgen levels in Chinese polycystic ovary syndrome patients with insulin resistance
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Genetic links between atopy, allergy, and alopecia areata: insights from a Mendelian randomization study
- DNA phenotyping: current application in forensic science
- Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema