Search
for
Sort by
Research 331–360 of 1000+
- Protein kinase C is a key target for attenuation of Leigh syndrome by rapamycin
- The involvement of androgens in human hair growth
- Association between genetically predicted rheumatoid arthritis and alopecia areata: a two-sample Mendelian randomization study
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- Cardiometabolic and neuroimaging correlates of cognitive function in polycystic ovary syndrome
- The genetic basis of dermatophytosis skin infection susceptibility
- Investigation Bisphenol A and Phthalate Levels in Idiopathic Hyperandrogenemia
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- POSTĘP W DIAGNOZIE I LECZENIU STWARDNIENIA ROZSIANEGO
- PŁYNY- NIE ZA DUŻO, NIE ZA MAŁO, LECZ W SAM RAZ
- ONKOLOGIA OKULISTYCZNA WCZORAJ I DZIŚ
- AUTOLOGOUS FAT GRAFTING UPDATE. PRESENTATION OF OWN RESULTS IN FACIAL REGENERATION
- MICRO-URZĄDZENIA, BEZPRZEWODOWE KAPSUŁKI, MAPY, STYMULATORY I ROZRUSZNIKI STOSOWANE DO DIAGNOSTYKI I LECZENIA ZABURZEŃ MOTORYKI PRZEWODU POKARMOWEGO
- EFFECTS OF LIRAGLUTIDE ON VISCERAL ADIPOSITY INDEX IN WOMAN OF REPRODUCTIVE AGE WITH PREDIABETES
- THE USE OF AN IMMUNOMODULATOR WITH AN ANTISEPTIC IN THE TREATMENT OF INFECTED AND PURULENT WOUNDS IN AN EXPERIMENT
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Efectos de la alteración de los niveles de allopregnanolona durante periodos críticos del neurodesarrollo en la vulnerabilidad al consumo de alcohol
- National scientific medical meeting 1996 abstracts
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Androgen receptors and their biology
- Androgenic Effects on Ventricular Repolarization
- Wnt signaling: the good and the bad
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Alopecia in Epidermolysis Bullosa
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Clinical characterization of men with long QT syndrome and torsades de pointes associated with hypogonadism: A review and pharmacovigilance study
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Atlas of Geriatric Dermatology
- Inherited Disorders of the Hair
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome