Search
for
Sort by
Research 151–180 of 503
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Dermatologic manifestations of endocrine disorders
- Prediction of male-pattern baldness from genotypes
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- 公表学術論文等リスト 2018
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Results of 60-second timed hair counts in women between the ages of 20–60 years
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- An Update of Congenital Adrenal Hyperplasia
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- 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
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- Urinary 5-ene-steroid excretion in non-classical congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency (NC-3BHSD)
- Evidence of a Causal Relationship Between Body Mass Index and Immune-Mediated and Inflammatory Skin Diseases and Biomarkers: A Mendelian Randomization Study
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- Serum sickness–like reaction in children: A retrospective review
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Measuring the impact on quality of life of infants with atopic dermatitis in a dedicated clinic
- Alopecia Areata