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Research 751–780 of 1000+
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- WNT10B (wingless-type MMTV integration site family)
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- The molecular basis of human keratin disorders
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Transcriptome Sequencing and Mass Spectrometry Reveal Genes Involved in the Non-mendelian Inheritance-Mediated Feather Growth Rate in Chicken
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Telomere dysfunction impairs epidermal stem cell specification and differentiation by disrupting BMP/pSmad/P63 signaling
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Physical and mechanical cues affecting biomaterial-mediated plasmid DNA delivery: insights into non-viral delivery systems
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- Quorum sensing and other collective regenerative behavior in organ populations
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- An evaluation of the RapidHIT™ ID system for hair roots stained with Diamond™ Nucleic Acid Dye
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells