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Research 271–300 of 1000+
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Inflammatory bowel disease: pathogenesis, diagnosis and current therapeutic approach
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Genetic analysis of a novel antioxidant multi-target iron chelator, M30 protecting against chemotherapy-induced alopecia in mice
- Construction of the coexpression network involved in the pathogenesis of thyroid eye disease via bioinformatics analysis
- Elucidation of the Potential Hair Growth-Promoting Effect of Botryococcus terribilis, Its Novel Compound Methylated-Meijicoccene, and C32 Botryococcene on Cultured Hair Follicle Dermal Papilla Cells Using DNA Microarray Gene Expression Analysis
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Expression of Signaling Components in Embryonic Eyelid Epithelium
- In Silico Analysis of the Age-Dependent Evolution of the Transcriptome of Mouse Skin Stem Cells
- Combining multiomics to analyze the molecular mechanism of hair follicle cycle change in cashmere goats from Inner Mongolia
- Is Dutasteride a Therapeutic Alternative for Amyotrophic Lateral Sclerosis?
- The relationship between keratin 18 and epithelial-derived tumors: as a diagnostic marker, prognostic marker, and its role in tumorigenesis
- Hair Growth-Promoting effect of the coffee bean residue extract on hair follicle dermal papilla cells via the activation of autophagy
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Antiviral drugs prolong survival in murine recessive dystrophic epidermolysis bullosa
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Oral Presentations
- A genetically informed brain atlas for enhancing brain imaging genomics
- <i>OsPHR2</i> Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
- The JAK/STAT signaling pathway: from bench to clinic
- Cutaneous wound healing: recruiting developmental pathways for regeneration
- Intratumoral <i>De Novo</i> Steroid Synthesis Activates Androgen Receptor in Castration-Resistant Prostate Cancer and Is Upregulated by Treatment with CYP17A1 Inhibitors
- Spermidine/spermine-<i>N</i><sup>1</sup>-acetyltransferase: a key metabolic regulator
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- Vitamin D: More Than a “Bone-a-Fide” Hormone
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- Eph Receptors and Ephrins: Therapeutic Opportunities
- On the Role of Melatonin in Skin Physiology and Pathology