Results 21 to 30 of about 2,624 (190)

Glomerular Exostosin-Positivity is Associated With Disease Activity and Outcomes in Patients With Membranous Lupus Nephritis [PDF]

open access: yesKidney International Reports
Introduction: The relationship of exostosin 1 and exostosin 2 (EXT1/EXT2) expression and outcomes in membranous lupus nephritis (MLN) was controversial.
Xi Xia   +9 more
doaj   +2 more sources

The potential of exogenous specialized pro-resolving mediators in protecting against sepsis-associated lung injury: a review [PDF]

open access: yesFrontiers in Pharmacology
Sepsis-associated lung injury (SALI) is a critical condition with high mortality. Current therapies are limited, necessitating novel approaches. This review highlights the potential of exogenous Specialized Pro-resolving Mediators (SPMs), including ...
Jiwei Shen   +26 more
doaj   +2 more sources

MAdLandExpression: integrating sexual reproduction into the Physcomitrium patens expression atlas. [PDF]

open access: yesPlant J
SUMMARY Physcomitrium patens is a bryophyte model system particularly valuable for evolutionary developmental and comparative genomics studies. Sexual reproduction in bryophytes offers unique insights into the evolution of land plant reproduction. Unlike seed plants, bryophytes have a dominant gametophyte phase and provide significant advantages for ...
Sanchez-Vera V   +9 more
europepmc   +2 more sources

Multiple osteochondromas of the antlers and cranium in a free-ranging white-tailed deer (Odocoileus virginianus) [PDF]

open access: yes, 2017
This paper reports a case of multiple osteochondromas affecting the antlers and the left zygomatic bone of a free-ranging adult white-tailed buck (Odocoileus virginianus) from Georgia, USA.
Flohr, Stefan   +4 more
core   +13 more sources

WCN24-2238 EXOSTOSIN 1- AND 2- POSITIVE MEMBRANOUS NEPHROPATHY IN CHINESE PATIENTS

open access: yesKidney International Reports
Hong Cheng   +13 more
doaj   +2 more sources

Multiple Heriditary Exostoses in a Family for Three Generation of Indian Origin with Review of Literature [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2014
Multiple hereditary exostoses (MHE) are an autosomal dominant disorder, consisting of multiple cartilage capped bone tumour arising from the metaphysis of long tubular bones. Mutations are seen in Exostosin-1 and Exostosin-2 genes.
Kalyani R   +4 more
doaj   +1 more source

Exostosin-1 enhances canonical Wnt signaling activity during chondrogenic differentiation [PDF]

open access: yesOsteoarthritis and Cartilage, 2019
Exostosin-1 (Ext1) encodes a glycosyltransferase required for heparan sulfate (HS) chain elongation in HS-proteoglycan biosynthesis. HS chains serve as binding partners for signaling proteins, affecting their distribution and activity. The Wnt/β-catenin pathway emerged as critical regulator of chondrogenesis.
Wang, X.   +3 more
openaire   +2 more sources

Exostosin-1 Glycosyltransferase Regulates Endoplasmic Reticulum Architecture and Dynamics [PDF]

open access: yes, 2020
SUMMARYThe endoplasmic reticulum (ER) is a central eukaryotic organelle with a tubular network made of hairpin proteins linked by hydrolysis of GTP nucleotides. Among post-translational modifications initiated at the ER level, glycosylation is the most common reaction.
Despoina Kerselidou   +30 more
openaire   +1 more source

Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses

open access: yesOrphanet Journal of Rare Diseases, 2021
Background Hereditary Multiple Exostoses (HME), also known as Multiple Osteochondromas (MO) is a rare genetic disorder characterized by multiple benign cartilaginous bone tumors, which are caused by mutations in the genes for exostosin ...
Zayed Al-Zayed   +9 more
doaj   +1 more source

Familial Nephropathy and Multiple Exostoses With Exostosin-1 (EXT1) Gene Mutation [PDF]

open access: yesJournal of the American Society of Nephrology, 2008
Glomerular deposition of fibrillar collagen is a characteristic finding of genetically distinct conditions, including nail-patella syndrome and collagen type III glomerulopathy. A case of familial nephropathy in which steroid-sensitive nephrotic syndrome and glomerular deposits of fibrillar collagen are associated with multiple exostoses due to ...
Ian S D, Roberts, Jonathan M, Gleadle
openaire   +2 more sources

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