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Research 601–630 of 1000+
- Identification of key genes induced by platelet-rich plasma in human dermal papilla cells using bioinformatics methods
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Isochromosome Mosaic Turner Syndrome: A Case Report
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Genetics of Diabetes in Childhood
- Terrestrial vertebrates have two keratin gene clusters; striking differences in teleost fish
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Epidermal Differentiation Complex: A Review on Its Epigenetic Regulation and Potential Drug Targets.
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Genetic prediction of male pattern baldness based on large independent datasets
- Complementary Strategies to Promote Hair Regrowth in Post-COVID-19 Telogen Effluvium
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- A novel eco-friendly Acinetobacter strain A1-4-2 for bioremediation of aquatic pollutants
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
- Exploring murE protein inhibitors of Tropheryma whipplei through pharmacoinformatic approaches incorporating solubility-enhancing formulation insights
- The Rationale for Inhibiting 5α-Reductase Isoenzymes in the Prevention and Treatment of Prostate Cancer
- Actinic keratosis: a clinical and epidemiological revision