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Research 241–270 of 1000+
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- MOESM1 of A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Identification of a Novel MPL Loss of Function Mutation in a Patient with Cyclic Thrombocytopenia and Characterization of This Syndrome
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Inflammatory Cytokine TNFα Promotes the Long-Term Expansion of Primary Hepatocytes in 3D Culture
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- Expression of Vimentin in hair follicle growth cycle of inner Mongolian Cashmere goats
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- Two novel CreER<sup>T2</sup> transgenic mouse lines to study melanocytic cells in vivo
- Hyperinnervation inhibits organ-level regeneration in mammalian skin
- Exosomal miRNA-218–5p derived from low-passage dermal papilla cells modulates hair follicle growth and development
- FGF5 is a crucial regulator of hair length in humans
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Transcriptome Analysis Reveals an Inhibitory Effect of Dihydrotestosterone-Treated 2D- and 3D-Cultured Dermal Papilla Cells on Hair Follicle Growth
- Forensic skeletal and molecular anthropology face to face: Combining expertise for identification of human remains
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- The potential role of hsa_circ_0001079 in androgenetic alopecia via sponging hsa‐miR‐136‐5p
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep