Search
for
Sort by
Research 391–420 of 1000+
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Matriptase: Potent Proteolysis on the Cell Surface
- Gene therapy to enhance angiogenesis in chronic wounds
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Nucleic acid-induced chemokine expression in keratinocytes: Implications for skin inflammation
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Entdeckung von Autoantigenen bei der Haarverluststörung Alopecia areata: Implikation von posttranslationalen Modifikationen
- Ku80 as a Novel Receptor for Thymosin β4 That Mediates Its Intracellular Activity Different from G-actin Sequestering
- Coming of Age of Melanogenesis-Related Proteins
- AabHLH112, a bHLH transcription factor, positively regulates sesquiterpenes biosynthesis in Artemisia annua
- Intramembrane Proteolysis of Astrotactins
- GDNF promotes hair formation and cutaneous wound healing by targeting bulge stem cells
- Fast Motions in 5 Alpha Reductase and Its Impact on Enzyme Kinetics
- Factors Associated with the Severity of Female Pattern Hair Loss: A Retrospective Study
- Injectable Dual‐Crosslinked Poly(oligo(Ethylene Glycol) Methacrylate) Hydrogels Inspired by Mussel Adhesion for Cutaneous Wound Healing and Functional Tissue Regeneration
- Structures of Get3d reveal a distinct architecture associated with the emergence of photosynthesis
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Premature aging syndromes: From patients to mechanism
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- The nude gene and the skin