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Research 301–330 of 1000+
- Insulin Resistance and Polycystic Ovary Syndrome
- 13. Wound Healing & Hair
- 5. HIV, Fungal and Infectious Diseases
- 6. Phototherapy, Photomedicine, and Pigmentary Disorders
- 4. Bullous/Mucous Membrane
- 1. Medical Practice; Therapy; Adverse Reactions
- 12. Cancer
- National scientific medical meeting 1996 abstracts
- Dermatoses of pregnancy
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Function and underlying mechanisms of seasonal colour moulting in mammals and birds: what keeps them changing in a warming world?
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- Idiopathic Hirsutism*
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- Oncogenic senescence: a multi-functional perspective
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- The Genetics of Human Skin Disease
- Female pattern hair loss
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Genetic basis of polycystic ovary syndrome
- A comparative analysis of immune privilege in pregnancy and cancer in the context of checkpoint blockade immunotherapy
- 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
- The Biology of Hair Growth
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- An update on diagnosis and treatment of female pattern hair loss
- Anorexia Nervosa and Bulimia Nervosa