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Research 451–480 of 1000+
- Comprehensive analysis of circRNAs from cashmere goat skin by next generation RNA sequencing (RNA-seq)
- Intelligent nanotherapeutic strategies for the delivery of CRISPR system
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Inflammatory perspectives of polycystic ovary syndrome: role of specific mediators and markers
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- <i>Igf1r</i> signalling acts on the anagen‐to‐catagen transition in the hair cycle
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- 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>)
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- The role of <i>Atg5</i> gene in tumorigenesis under autophagy deficiency conditions
- Hub biomarkers in ultrasound-guided bladder cancer and osteosarcoma: Myosin light chain kinase and caldesmon
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- TRPV3 Ion Channel: From Gene to Pharmacology
- Mild oxidative stress protects against chemotherapy-induced hair loss
- MiR-199a-3p Regulates the PTPRF/β-Catenin Axis in Hair Follicle Development: Insights into the Pathogenic Mechanism of Alopecia Areata