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Research 151–180 of 1000+
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism
- Highly Conserved Keratin-Associated Protein 7-1 Gene in Yak, Taurine and Zebu Cattle
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Helminth protein enhances wound healing by inhibiting fibrosis and promoting tissue regeneration
- Mechanisms that regulate androgen receptor transcriptional activity
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- Genome-wide analysis of Musashi-2 targets reveals novel functions in governing epithelial cell migration
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- NOVEL CORONAVIRUS (SARS-COV-2): MOLECULAR BIOLOGY, PATHOGENESIS, PATHOBIOLOGY AND ADVANCES IN TREATMENT OF COVID-19 PATIENTS– AN UPDATE
- Telogen hair loss and androgenetic‐like alopecia in GAPO syndrome
- Novel Formula as Mosquito Larvicide
- Reconstructing protein conformations to activate follicular enzyme-nutrient reservoirs for reversing follicle aging
- Hair Growth Promoting Effects of Limosilactobacillus reuteri Isolated from Honeybee through Wnt/β-catenin Signal Transduction
- Comparative Evaluation of Systemic and Hair Growth Pathways for the Detection and Assessment of Chronic Stress
- Genes for intermediate filament proteins and the draft sequence of the human genome
- Sustained Exosome‐Guided Macrophage Polarization Using Hydrolytically Degradable PEG Hydrogels for Cutaneous Wound Healing: Identification of Key Proteins and MiRNAs, and Sustained Release Formulation
- Isolation and Characterization of Mouse High-glycine/Tyrosine Proteins
- Exosomes as a novel pathway for regulating development and diseases of the skin (Review)
- Charting the Bromodomain BRD4: Towards the Identification of Novel Inhibitors with Molecular Similarity and Receptor Mapping
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Ca <sup>2+</sup> -mediated protein citrullination regulates proliferation in the regenerating and malignant CNS
- Functionally enhanced placenta-derived mesenchymal stem cells inhibit adipogenesis in orbital fibroblasts with Graves’ ophthalmopathy
- Analysis of Protein Interactions by Surface Plasmon Resonance
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- A Ca <sup>2+</sup> /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- The deduced sequence of the novel protransglutaminase E (TGase3) of human and mouse