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Research 91–120 of 1000+
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Investigating RNA-Seq-based differential gene expression during hair follicle development in Angora goat skin
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Newborn infant skin gene expression: Remarkable differences versus adults
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- The Use of Stem Cell Differentiation Stage Factors (SCDSFs) Taken from Zebrafish Embryos during Organogenesis and Their Role in Regulating the Gene Expression of Normal and Pathological (Stem) Cells
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Seasonal Gene Expression Profile Responsible For Hair Follicle Development In Angora Goats
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study
- Gene Variant in Amish a Clue to Better Aging
- Keratin disorders: from gene to therapy
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- The expression of the gene <i>asebia</i> in the laboratory mouse: 3. Sebaceous glands
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Disease causing homozygous variants in the human hairless gene
- Performance exploration of multi-gene panels of alopecia areata susceptibility and drug-binding targets
- Inhibition of Inflammatory Gene Expression in Keratinocytes Using a Composition Containing Carnitine, Thioctic Acid and Saw Palmetto Extract
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans