Showing results (11-20 of 54) with videos related to
Sort By:
Pageof 6
Circulation. Cardiovascular Genetics|February 16, 2017
Hyaluronidase 2 Deficiency Causes Increased Mesenchymal Cells, Congenital Heart Defects, and Heart FailureBiswajit Chowdhury, Bo Xiang, Michelle Liu, et al.Biochimica Et Biophysica Acta|May 3, 2015
Increase of a group of PTC(+) transcripts by curcumin through inhibition of the NMD pathwayDairong Feng, Ruey-Chyi Su, Liping Zou, et al.Atherosclerosis|January 22, 2018
The natural history of phytosterolemia: Observations on its homeostasisDavid Mymin, Gerald Salen, Barbara Triggs-Raine, et al.Matrix Biology : Journal of the International Society for Matrix Biology|June 26, 2010
The C. elegans hyaluronidase: a developmentally significant enzyme with chondroitin-degrading activity at both acidic and neutral pHAllison Chatel, Rick Hemming, Judith Hobert, et al.Biochemical and Biophysical Research Communications|September 5, 2012
The adult polyglucosan body disease mutation GBE1 c.1076A>C occurs at high frequency in persons of Ashkenazi Jewish backgroundAbrar Hussain, Joy Armistead, Lara Gushulak, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 6, 2008
Skeletal and hematological anomalies in HYAL2-deficient mice: a second type of mucopolysaccharidosis IX?Laurence Jadin, Xiaoli Wu, Hao Ding, et al.Glycobiology|February 1, 2008
Mouse Hyal3 encodes a 45- to 56-kDa glycoprotein whose overexpression increases hyaluronidase 1 activity in cultured cellsRichard Hemming, Dianna C Martin, Elzbieta Slominski, et al.Journal of Cellular Physiology|July 7, 2011
Hyal-1 but not Hyal-3 deficiency has an impact on ovarian folliculogenesis and female fertility by altering the follistatin/activin/Smad3 pathway and the apoptotic processKarine Dumaresq-Doiron, Lydia Edjekouane, Adriana Mari Orimoto, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 9, 2021
Bitter taste receptor T2R14 detects quorum sensing molecules from cariogenic Streptococcus mutans and mediates innate immune responses in gingival epithelial cellsManoj Reddy Medapati, Nisha Singh, Anjali Yadav Bhagirath, et al.Journal of Inherited Metabolic Disease|May 12, 2011
A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritisLisa Imundo, Charles A Leduc, Saurav Guha, et al.Pageof 6