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Research 61–90 of 1000+
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Causal relationship between gut microbiota and androgenetic alopecia: A Mendelian randomization study
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- MITF E318K naevus phenotype: the modifying role of MC1R Red Hair Variants
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- SLE classification criteria item relationships: implications on SLE as a disease entity
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Mendelian Randomization Identifies CD25+ CD4+ Tregs and Plasma Proteins in Androgenetic Alopecia Pathogenesis
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Evaluation of Retinal Changes in Women with Different Phenotypes of Polycystic Ovary Syndrome
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- 132 Genetics of Stress Hormone Concentrations in Hair of Healthy Nursery Pigs and Their Relationship with Back Test Responses
- Betaine supplementation is less effective than methionine restriction in correcting phenotypes of CBS deficient mice
- Hair follicle morphogenesis and epidermal homeostasis in we/we wal/wal mice with postnatal alopecia
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Spatiotemporal regulation of acute wound healing by the NLRP3 inflammasome: dual roles in macrophage-fibroblast chemotaxis and phenotype during wound repair
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Molecular characterization of GhPLDα1 and its relationship with secondary cell wall thickening in cotton fibers
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Psoriasis patients demonstrate HLA-Cw*06:02 allele dosage-dependent T cell proliferation when treated with hair follicle-derived keratin 17 protein
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- A missense mutation in Lama3 causes androgen alopecia
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk