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Research 811–840 of 1000+
- Resistance of degraded hair shafts to contaminant DNA
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Dynamic changes of genomic methylation profiles at different growth stages in Chinese Tan sheep
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Minoxidil may suppress androgen receptor-related functions
- Developmental genetics of color pattern establishment in cats
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- ALKBH5-mediated m6A demethylation fuels cutaneous wound re-epithelialization by enhancing PELI2 mRNA stability
- Shedding light on cashmere goat hair follicle biology: from morphology analyses to transcriptomic landascape
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Integrated analysis of miRNAs and mRNA profiling reveals the potential roles of miRNAs in sheep hair follicle development
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep