Search
for
Sort by
Research 541–570 of 1000+
- Ovine KRT81 Variants and Their Influence on Selected Wool Traits of Commercial Value
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- S100A6: molecular function and biomarker role
- Self-consistent field theory for the interactions between keratin intermediate filaments
- Identification and Analysis of MYB Gene Family for Discovering Potential Regulators Responding to Abiotic Stresses in Curcuma wenyujin
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Mesenchymal Stem Cells With Modification of Junctional Adhesion Molecule A Induce Hair Formation
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- The Catalog of Human Hair Keratins
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Immunization by Application of DNA Vaccine onto a Skin Area Wherein the Hair Follicles Have Been Induced into Anagen-onset Stage
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Regulation of Keratin Gene Expression in Hair Follicle Differentiation<sup>a</sup>
- Organization and Expression of Hair Follicle Genes.
- Sequence, expression, and evolutionary conservation of a gene encoding a glycine/tyrosine-rich keratin-associated protein of hair.
- Allosteric interactions prime androgen receptor dimerization and activation
- Docosahexaenoic acid-acylated astaxanthin esters alleviate cisplatin- induced acute kidney injury by modulating the ferroptosis-related GPX4/xCT signaling pathway and reducing oxidative stress
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Type II Keratins Are Phosphorylated on a Unique Motif during Stress and Mitosis in Tissues and Cultured Cells
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- In Silico Promoter Motif Analysis of Human Fertility-Related Genes
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Folliculotropic Mycosis Fungoides with Skewed T-cell Receptor CDR3 Motif: Suggestive of Lipid-antigen Selection?
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis