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Research 391–420 of 499
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Molecular Basis of Androgenetic Alopecia
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Sex-limited chromosomes and non-reproductive traits
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- A Case of Frontal Fibrosing Alopecia in a Patient with Primary Biliary Cirrhosis and Polymyalgia Rheumatica
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Study of the Thyroid Profile of Patients with Alopecia
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Food Administration and Not Genetic Variants Causes Pharmacokinetic Variability of Tadalafil and Finasteride
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- First Symposium of Ichthyosis Experts
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Sex Differences in Reaction to Chronic Unpredictable Stress in the House Mouse (Mus musculus musculus) of Wild Origin
- Stress-induced sympathetic hyperactivation drives hair follicle necrosis to trigger autoimmunity
- Clinicopathological factors associated with trichilemmal cysts
- Sex Differences in Reaction to Chronic Unpredictable Stress in the House Mouse (<em>Mus m. musculus</em>) of Wild Origin
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep