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Research 631–660 of 1000+
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- 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>)
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Siberian cats help in solving part of the mystery surrounding golden cats
- Sox13 is a novel early marker for hair follicle development
- Cellular Senescence and Aging in Myotonic Dystrophy
- ELL Facilitates RNA Polymerase II–Mediated Transcription of Human Epidermal Proliferation Genes
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Promoter Methylation Changes in KRT17: A Novel Epigenetic Marker for Wool Production in Angora Rabbit
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Hair follicle epithelial stem cells contribute to interfollicular epidermis during homeostasis
- Steatocystoma Multiplex
- Large-Scale, Multicenter, Prospective Registry Study of Ripretinib in Advanced GIST: A Real-World Study from China
- Androgens/Androgen Receptor in the Management of Skin Diseases
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings
- Integrative skin phenotypic and transcriptomic analyses reveal candidate genes for coat color and fiber length in four Chinese goat breeds (<i>Capra hircus</i>)
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Exploring lncRNA-Mediated Mechanisms in Muscle Regulation and Their Implications for Duchenne Muscular Dystrophy
- Signal integrator function of CXXC5 in Cancer