Search
for
Sort by
Research 181–210 of 1000+
- LncRNA018392 promotes proliferation of Liaoning cashmere goat skin fibroblasts through up-regulation of CSF1R by binding to SPI1
- Transforming 300 billion points of data into diagnostics, therapeutics and new insights into disease
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Current Genetics in Hair Diseases
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Expression profile analysis of microRNAs during hair follicle development in the sheep foetus
- Comprehensive Transcriptome Analysis of Hair Follicle Morphogenesis Reveals That lncRNA-H19 Promotes Dermal Papilla Cell Proliferation through the Chi-miR-214-3p/β-Catenin Axis in Cashmere Goats
- Melatonin’s Role in Hair Follicle Growth and Development: A Cashmere Goat Perspective
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Novel potential therapeutic targets of alopecia areata
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- Single-cell RNA-seq highlights heterogeneity in human primary Wharton’s jelly mesenchymal stem/stromal cells cultured in vitro
- The role of WNT10B in physiology and disease: A 10-year update
- Skin microbiota and diabetic foot ulcers
- Autophagy protects murine preputial glands against premature aging, and controls their sebum phospholipid and pheromone profile
- Sex Differences in Reaction to Chronic Unpredictable Stress in the House Mouse (Mus musculus musculus) of Wild Origin
- African Journal of Biomedical Research
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China