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- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- The Effect of Hairless Mutant Gene on The Thymus and Skin Under The C_(57)BL/6 Genetic Background
- Pathogenesis of androgenetic alopecia
- Using Lever to Foster Health and Wellness and Inducing Comfort in Genetic Health Ailment of Head Baldness
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Hair Sciences: The hair cycle discussed with Dr. Gilliam Westgate
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- The molecular puzzle of autoinflammatory skin diseases—a review of chosen conditions
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Genetics of Progeria and Aging
- Androgenic alopecia in men: the significance of genetic, hormonal and metabolic factors (prospective cohort comparative study)
- Genetic Fate Mapping Using Site-Specific Recombinases
- Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles
- Item Analysis of the Japanese Version of the Generic Health-related Quality of Life Questionnaire for Children and Adolescents : Kid-KINDL-R and Kiddo-KINDL-R
- Effect of PTPN22, FAS/FASL, IL2RA and CTLA4 genetic polymorphisms on the risk of developing alopecia areata: A systematic review of the literature and meta-analysis
- Senescence-accelerated Mouse (SAM): With Special Reference to Development and Pathobiological Phenotypes
- Etiopathogenesis of Alopecia Areata
- Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Prevalence and characteristics of polycystic ovary syndrome in Brazilian women: protocol for a nation-wide case–control study
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Hair science and technology
- Marie-unna hereditary hypotrichosis
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Defining the Cellular Environment in the Organ of Corti following Extensive Hair Cell Loss: A Basis for Future Sensory Cell Replacement in the Cochlea
- [Visual field defect in a patient given sodium valporate then carbamazepine: possible effect of aminotransferase inhibition].
- Research Relevant Conditions and Pathology in Nonhuman Primates