Zobrazeno 1 - 10
of 79
pro vyhledávání: '"DTDST, diastrophic dysplasia sulfate transporter"'
Publikováno v:
The Journal of Biological Chemistry
Fibronectin (FN), an essential component of the extracellular matrix (ECM), is assembled via a cell-mediated process in which integrin receptors bind secreted FN and mediate its polymerization into fibrils that extend between cells, ultimately formin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a814e97b6c25bd5dfe573021712f6e7
http://europepmc.org/articles/PMC8801470
http://europepmc.org/articles/PMC8801470
Autor:
Valérie Geoffroy, Fabio De Leonardis, Marie-Christine de Vernejoul, Caroline Marty-Morieux, Luca Monti, Pascal Houillier, Marco Franchi, Antonio Rossi, Benedetta Gualeni, Antonella Forlino
Publikováno v:
Bone
Diastrophic dysplasia (DTD) is a chondrodysplasia caused by mutations in the SLC26A2 gene, leading to reduced intracellular sulfate pool in chondrocytes, osteoblasts and fibroblasts. Hence, proteoglycans are undersulfated in the cartilage and bone of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c79af51f0b82233a5a30182dcb5c9122
http://hdl.handle.net/11585/292327
http://hdl.handle.net/11585/292327
Autor:
Lee, Dongun1 (AUTHOR) sppotato1@gmail.com, Hong, Jeong Hee1 (AUTHOR) minicleo@gachon.ac.kr
Publikováno v:
International Journal of Molecular Sciences. Apr2024, Vol. 25 Issue 8, p4190. 16p.
Autor:
Sabir, Ataf H.1,2 (AUTHOR) ataf.sabir2@nhs.net, Morley, Elizabeth3 (AUTHOR), Sheikh, Jameela2 (AUTHOR), Calder, Alistair D.4 (AUTHOR), Beleza-Meireles, Ana5 (AUTHOR), Cheung, Moira S.6 (AUTHOR), Cocca, Alessandra6 (AUTHOR), Jansson, Mattias7 (AUTHOR), Lillis, Suzanne7 (AUTHOR), Patel, Yogen8 (AUTHOR), Yau, Shu7 (AUTHOR), Hall, Christine M.9,10 (AUTHOR), Offiah, Amaka C.11 (AUTHOR), Irving, Melita1,12 (AUTHOR)
Publikováno v:
BMC Medical Genomics. 12/1/2021, Vol. 14 Issue 1, p1-14. 14p.
The role of NHE3 (Slc9a3) in oxalate and sodium transport by mouse intestine and regulation by cAMP.
Autor:
Stephens, Christine E.1 (AUTHOR) cstephens343@googlemail.com, Whittamore, Jonathan M.1 (AUTHOR), Hatch, Marguerite1 (AUTHOR)
Publikováno v:
Physiological Reports. Apr2021, Vol. 9 Issue 7, p1-19. 19p.
Autor:
Jonathan Celli Honório, Rafael Frederico Bruns, Luciana Fernandes Gründtner, Salmo Raskin, Lilian Pereira Ferrari, Edward Araujo Júnior, Luciano Marcondes Machado Nardozza
Publikováno v:
São Paulo Medical Journal, Vol 131, Iss 2, Pp 127-132 (2013)
CONTEXT Diastrophic dysplasia is a type of osteochondrodysplasia caused by homozygous mutation in the gene DTDST (diastrophic dysplasia sulfate transporter gene). Abnormalities occurring particularly in the skeletal and cartilaginous system are typic
Externí odkaz:
https://doaj.org/article/4da7aef22b51409facddea5a668d02e3
Publikováno v:
Czecho-Slovak Pathology & Forensic Medicine / Česko-Slovenská Patologie a Soudní Lékařství; Apr2023, Vol. 59 Issue 2, p68-79, 12p
Publikováno v:
Pflügers Archiv: European Journal of Physiology; Feb2023, Vol. 475 Issue 2, p249-266, 18p
Publikováno v:
Frontiers in Genetics; 6/16/2021, Vol. 11, p1-28, 28p
Publikováno v:
Seminars in Musculoskeletal Radiology; 2021, Vol. 25 Issue 2, p260-271, 12p