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Research 391–420 of 1000+
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Genome-Wide Association Study for Body Conformation Traits in Kazakh Fat-Tailed Coarse-Wool Sheep
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Cantú Syndrome Is Caused by Mutations in ABCC9
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- A Genetically Defined Male Counterpart of Polycystic Ovary Syndrome: Evidence for Ovarian-Independent Pathogenesis
- Discriminative models of the possibility of occurrence and features of the course of alopecia areata in Ukrainian men depending on the features of body structure and size indicators
- Serum Level of Galectin -3 and Its Relation to Insulin Resistance in Patients with Androgenetic Alopecia
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Epidermal pigmentation in the human lineage is an adaptation to ultraviolet radiation
- Uveodermatological syndrome in dogs: A review of diagnosis, management, and ophthalmic patient needs
- A curated catalog of canine and equine keratin genes
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Genetically determined metabolites in allergic conjunctivitis: A Mendelian randomization study
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- A missense mutation in Lama3 causes androgen alopecia
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- Predictive factors for therapeutic response and cluster analysis in syndrome of undifferentiated recurrent fever (SURF)
- How to Choose the Optimal Starting Dose of Clomiphene Citrate (50 or 100 mg per Day) for a First Cycle of Ovulation Induction in Anovulatory PCOS Women?