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Research 91–120 of 1000+
- National scientific medical meeting 1996 abstracts
- Posters Presented at the 19th Joint Meeting of the International Society of Dermatopathology, March 2–3, 2016, Hilton Crystal City at Washington Reagan National Airport, Arlington, Virginia, USA
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Correlation Between Nongenomic Action of C19-Steroids and COVID-19 Severity
- Clinical and Histopathological Features and Potential Pathological Mechanisms of Skin Lesions in COVID-19: Review of the Literature
- Testosterone target therapy: focus on immune response, controversies and clinical implications in patients with COVID-19 infection
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Basonuclin is associated with the ribosomal RNA genes on human keratinocyte mitotic chromosomes
- Insertional mutation of the hairless locus on mouse Chromosome 14
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- The Shaven (Sha) Mutation, Chromosome 15
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Male-pattern baldness susceptibility locus at 20p11
- Do Changes in Chromosomes Cause Aging?
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- Immuno-Endocrinology of COVID-19: The Key Role of Sex Hormones
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- COVID-19 Severity and Androgen Receptor Polymorphism
- Marie-unna hereditary hypotrichosis
- Complementary Strategies to Promote Hair Regrowth in Post-COVID-19 Telogen Effluvium
- Alopecia Areata is associated with MICA and an extended HLA haplotype