Results 11 to 20 of about 70,103 (68)

Signature of a partnership agreement between ISPD and RDPLF for French translation of ISPD guidelines.

open access: yes, 2021
We are pleased to announce with this new issue of the Bulletin de la Dialysis à Domicile (BDD), the bilingual journal of the RDPLF, the recent signing of a partnership agreement between the International Society of Peritoneal Dialysis (ISPD) and the ...
Max Dratwa, Christian Verger
core   +2 more sources

Human ISPD Is a Cytidyltransferase Required for Dystroglycan O-Mannosylation. [PDF]

open access: yes, 2015
A unique, unsolved O-mannosyl glycan on α-dystroglycan is essential for its interaction with protein ligands in the extracellular matrix. Defective O-mannosylation leads to a group of muscular dystrophies, called dystroglycanopathies.
Kopec, Jolanta   +18 more
core   +4 more sources

Francisella tularensis IspD: A Target for Novel Antibiotics [PDF]

open access: yes, 2013
Francisella tularensis is the pathogenic bacteria responsible for causing Tularemia, a severe disease that has been explored as a biological weapon, leading to its classification as a Category A bioterrorist agent.
Tsang, Arthur
core   +1 more source

Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of alpha-dystroglycan [PDF]

open access: yes, 2012
Contains fulltext : 108772.pdf (Publisher’s version ) (Open Access)Walker-Warburg syndrome (WWS) is an autosomal recessive multisystem disorder characterized by complex eye and brain abnormalities with congenital muscular dystrophy (CMD)
van Reeuwijk, Jeroen   +173 more
core   +2 more sources

ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases [PDF]

open access: yes, 2015
Background: Limb Girdle Muscular Dystrophy (LGMD), caused by defective aα-dystroglycan (aα-DG) glycosylation, was recently associated with mutations in Isoprenoid synthase domain-containing (ISPD) and GDP-mannose pyrophosphorylase B (GMPPB) genes.
D. Ronchi   +12 more
core   +1 more source

gapdh mutations do not confer resistance to the IspD inhibitor MMV008138.

open access: yes, 2022
MMV008138 inhibits the MEP pathway enzyme IspD competitively with its CTP substrate. Summary EC50 data, determined using GraphPad Prism non-linear regression. (TIFF)
Naomi Ghebremichael (9578319)   +6 more
core   +1 more source

Scheduler simulation using iSPD, an iconic-based computer grid simulator

open access: yes, 2012
Increased accessibility to high-performance computing resources has created a demand for user support through performance evaluation tools like the iSPD (iconic Simulator for Parallel and Distributed systems), a simulator based on iconic modelling for ...
Da Silva, Diogo T.   +12 more
core   +1 more source

Characterization and inhibitor evaluation of IspD and IspE enzymes from the non-mevalonate pathway [PDF]

open access: yes, 2016
There is an immediate need for new antibiotics. Antimicrobial resistance is rising at an alarming rate. In addition, certain select agents are a risk for bioterrorism that necessitate the discovery of new antibiotics. The methylerythritol phosphate (MEP)
Hartnett, Brian E.
core   +1 more source

ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto α-dystroglycan

open access: yes, 2016
Mutations in genes required for the glycosylation of α-dystroglycan lead to muscle and brain diseases known as dystroglycanopathies. However, the precise structure and biogenesis of the assembled glycan are not completely understood.
Cuisset, J. M.   +31 more
core   +1 more source

Otorbiające stwardnienie otrzewnej — stanowisko ISPD, aktualizacja z 2017 roku [PDF]

open access: yes, 2019
Encapsulating peritoneal sclerosis is a rare, but asso­ciated with high morbidity and mortality complication on long-term peritoneal dialysis (PD).
Małyszko, Jolanta; Katedra i Klinika Nefrologii, Dializoterapii i Chorób Wewnętrznych, Warszawski Uniwersytet Medyczny   +2 more
core  

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