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Research 931–960 of 1000+
- Characterisation of Myotonic Dystrophy type I cell models and drug evaluation by a cell- based quantification platform.
- Differences in Demographic and Clinical Characteristics Among Subtypes of Female Pattern Hair Loss
- ASSOCIATION BETWEEN AB0 BLOOD TYPE SYSTEM WITH A HEMOGLOBIN LEVEL IN BLOOD AND IRON CONCENTRATION IN HAIR
- WNT10B (wingless-type MMTV integration site family)
- Ku80 as a Novel Receptor for Thymosin β4 That Mediates Its Intracellular Activity Different from G-actin Sequestering
- Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- AS FINALIDADES TERAPÊUTICAS DA TOXINA BOTULÍNICA TIPO A
- Author response: Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- Decision letter: Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- Genetics of Diabetes in Childhood
- FC053 Pro-inflammatory cytokine cascade in human plucked hair
- Cytokeratin expression in trichoblastic fibroma (small nodular type trichoblastoma), trichoepithelioma and basal cell carcinoma
- Alopecia and Semaglutide: Connecting the Dots for Patient Safety
- 5175 A Rare Case of Type B Insulin Resistance Syndrome
- Frontal fibrosing alopecia: follow-up of a brazilian group
- 1640: Polymorphisms in the 5α-Reductase Type 2 Gene and Response to Finasteride Treatment in BPH
- Dihydrotestosterone and the Concept of 5α–Reductase Inhibition in Human Benign Prostatic Hyperplasia
- Diabetes and cardiovascular events in women with polycystic ovary syndrome: a 20-year retrospective cohort study
- Equine 5α-reductase activity and expression in epididymis
- Alopecia secondary to severe discoid lupus responding to anifrolumab
- MON-317 Prognostic Factors and Mortality According to the Structural and Functional Classification of Acromegaly
- A review on laser and light-based therapies for alopecia areata
- The Browning of White Adipose Tissue: Some Burning Issues
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- Diagnosis of Polycystic Ovary Syndrome
- Selenium for preventing cancer
- Scientific opinion on the tolerable upper intake level for selenium
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- Metabolic syndrome in Greek women with polycystic ovary syndrome: prevalence, characteristics and associations with body mass index. A prospective controlled study
- Bioextracting Polyphenols from the Brown Seaweed <i>Ascophyllum nodosum</i> from Québec's North Shore Coastline