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Research 751–780 of 1000+
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Construction of the coexpression network involved in the pathogenesis of thyroid eye disease via bioinformatics analysis
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Sex‐dependent responsiveness of hippocampal neurons to sex neurosteroids: A role of Arc/Arg3.1
- Knockout of the ING5 epigenetic regulator confirms roles in stem cell maintenance and tumor suppression in vivo
- The Enticing Path of miR Therapeutics: Difficult but Not without Prospects
- Efficient expansion of human keratinocyte stem/progenitor cells carrying a transgene with lentiviral vector
- High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Case-Only Trees and Random Forests for Exploring Genotype-Specific Treatment Effects in Randomized Clinical Trials with Dichotomous End Points
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- CRISPR/Cas9-mediated<i>VDR</i>knockout plays an essential role in the growth of dermal papilla cells through enhanced relative genes
- PCSK9: From Nature’s Loss to Patient’s Gain
- Palatogenesis and cutaneous repair: A two‐headed coin
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- Differential transcriptome study on the damage of testicular tissues caused by chronic infection of T. gondii in mice
- FOXN1 deficient nude severe combined immunodeficiency
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Network-based identification genetic effect of SARS-CoV-2 infections to Idiopathic pulmonary fibrosis (IPF) patients
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome