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Research 31–60 of 1000+
- Is polycystic ovary syndrome a sexual conflict? A review
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Disease causing homozygous variants in the human hairless gene
- Aberrant inflammasome activation as a driving force of human autoimmune skin disease
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Somatic mutations distinguish melanocyte subpopulations in human skin
- Significant improvement with ivarmacitinib after suboptimal response to tofacitinib in severe alopecia areata: a case report and literature review
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Androgen Receptor (<i>AR</i>) Gene (CAG)n and (GGN)n Length Polymorphisms and Symptoms in Young Males With Long-Lasting Adverse Effects After Finasteride Use Against Androgenic Alopecia
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Atopic dermatitis and risk of autoimmune diseases: a systematic review and meta-analysis
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- Dermatological Manifestations of Celiac Disease: a Literature Review
- The Rotterdam Study: 2016 objectives and design update
- Genetic prediction of male pattern baldness
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Dermatoses of Pregnancy - Clues to Diagnosis, Fetal Risk and Therapy
- Pathways to inflammation: acne pathophysiology
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation