Search
for
Sort by
Research 961–990 of 1000+
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Autophagy protects murine preputial glands against premature aging, and controls their sebum phospholipid and pheromone profile
- ROBO4 deletion ameliorates PAF-mediated skin inflammation via regulating the mRNA translation efficiency of LPCAT1/LPCAT2 and the expression of PAF receptor
- Runx Family Genes in Tissue Stem Cell Dynamics
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- Prefrontal 5α-reductase 2 mediates male-specific acute stress response
- Integrative analysis of Iso-Seq and RNA-seq data reveals transcriptome complexity and differential isoform in skin tissues of different hair length Yak
- Enhancing diabetic wound healing: advances in electrospun scaffolds from pathogenesis to therapeutic applications
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Regulatory network of ginsenoside biosynthesis under Ro stress in the hairy roots of Panax ginseng revealed by RNA sequencing
- Integrated analysis of miRNAs and mRNA profiling reveals the potential roles of miRNAs in sheep hair follicle development
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Wnt/β-Catenin Signaling Stabilizes Hemidesmosomes in Keratinocytes
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- SPRY1 Deficiency in Keratinocytes Induces Follicular Melanocyte Stem Cell Migration to the Epidermis through p53/Stem Cell Factor/C-KIT Signaling
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Physiology of Testicular Function
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Cellular Senescence and Aging in Myotonic Dystrophy
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Neutrophil extracellular traps impair regeneration
- ELL Facilitates RNA Polymerase II–Mediated Transcription of Human Epidermal Proliferation Genes
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Spatiotemporal Labeling of Melanocytes in Mice
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless