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Research 181–210 of 1000+
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
- Forensic skeletal and molecular anthropology face to face: Combining expertise for identification of human remains
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Pathology of Mouse Models of Accelerated Aging
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Differential cold stress intensities drive unique morphological and transcriptomic changes in Zea mays root hairs
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Drug repurposing—a promising approach for patients with angina but non-obstructive coronary artery disease (ANOCA)
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Cystathionine β‐synthase‐deficient mice thrive on a low‐methionine diet
- Is There a Histone Code for Cellular Quiescence?
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Relevance of the Axis Spermidine/eIF5A for Plant Growth and Development
- Exploring the relationship between anastasis and mitochondrial ROS-mediated ferroptosis in metastatic chemoresistant cancers: a call for investigation
- Cutaneous gene therapy
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- Highlighting nuances of blue light phototherapy: Mechanisms and safety considerations
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection