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Research 871–900 of 1000+
- Interactions between epidermal growth factor and the <i>Tabby</i> mutation in skin
- Systemic testosterone induces structural, immunological, and sex steroid receptor changes in human XX skin
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- Recent advances in congenital ichthyoses
- Polycystic ovary syndrome
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Prediction of male-pattern baldness from genotypes
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Restoring neuropetide Y levels in the hypothalamus ameliorates premature aging phenotype in mice
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Hair phenotype diversity across Indriidae lemurs
- The Polycystic Ovary Syndrome - Challenges and Opportunities in Adolescent Medicine
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Timing of expression of the core clock gene <i>Bmal1</i> influences its effects on aging and survival
- Weakly supervised learning of biomedical information extraction from curated data
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Relationship of Early-Onset Baldness to Prostate Cancer in African-American Men
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- Betaine supplementation is less effective than methionine restriction in correcting phenotypes of CBS deficient mice