Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Katsiaryna Belaya"'
Autor:
Vítor Trovisco, Katsiaryna Belaya, Dmitry Nashchekin, Uwe Irion, George Sirinakis, Richard Butler, Jack J Lee, Elizabeth R Gavis, Daniel St Johnston
Publikováno v:
eLife, Vol 5 (2016)
bicoid mRNA localises to the Drosophila oocyte anterior from stage 9 of oogenesis onwards to provide a local source for Bicoid protein for embryonic patterning. Live imaging at stage 9 reveals that bicoid mRNA particles undergo rapid Dynein-dependent
Externí odkaz:
https://doaj.org/article/37ba1074fd7d4884982f0fffcb81e35b
Autor:
J. Cheung, Todd A. Hardy, Nidhi Garg, Stephen W. Reddel, Katsiaryna Belaya, David Beeson, Con Yiannikas
Publikováno v:
Muscle & Nerve. 54:721-727
INTRODUCTION Congenital myasthenic syndromes (CMS) usually present neonatally or in early childhood. When they present later, they may be mistaken for seronegative autoimmune myasthenia, and unnecessary immunosuppressive treatment may be administered
Autor:
Vítor Trovisco, Richard Butler, Uwe Irion, Dmitry Nashchekin, Katsiaryna Belaya, Daniel St Johnston, Elizabeth R. Gavis, George Sirinakis, Jack J. Lee
Publikováno v:
eLife, Vol 5 (2016)
eLife
eLife
bicoid mRNA localises to the Drosophila oocyte anterior from stage 9 of oogenesis onwards to provide a local source for Bicoid protein for embryonic patterning. Live imaging at stage 9 reveals that bicoid mRNA particles undergo rapid Dynein-dependent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e18719376e9282d3e0938befa85fd223
Autor:
Hua Wang, N.A. Burgess-Brown, Katsiaryna Belaya, Sylvain F. Royer, Sadra Hamedzade, Andaleeb Sajid, S.R. Bushell, Shahid Mehmood, Ashley C. W. Pike, Takuya Machida, Wei Wei Liu, Carol V. Robinson, David Beeson, Wei-Min Liu, Y.Y. Dong, Mervyn J. Bibb, Benjamin G. Davis, David A. Widdick, Seung Seo Lee, Filip J. Wyszynski, Shubhashish M.M. Mukhopadhyay, Clifton E. Barry, Elisabeth P. Carpenter, Leela Shrestha, Ricardo Lucas, Helena I. Boshoff, Stephen A. Cochrane, A. Chu
SummaryProtein glycosylation is a widespread post-translational modification. The first committed step to the lipid-linked glycan used for this process is catalysed by dolichyl-phosphate N-acetylglucosamine-phosphotransferase DPAGT1 (GPT/E.C. 2.7.8.1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::276ba68a90e798d26899fbe7f2ff3797
Autor:
Shahid Mehmood, Ricardo Lucas, Sadra Hamedzadeh, Helena I. Boshoff, Mervyn J. Bibb, Stephen A. Cochrane, N.A. Burgess-Brown, Hua Wang, A. Chu, S.R. Bushell, David Beeson, Katsiaryna Belaya, Wei Wei Liu, Sylvain F. Royer, Andaleeb Sajid, Ashley C. W. Pike, Elisabeth P. Carpenter, Takuya Machida, Leela Shrestha, David A. Widdick, Benjamin G. Davis, Seung Seo Lee, Clifton E. Barry, Shubhashish M.M. Mukhopadhyay, Filip J. Wyszynski, Y.Y. Dong, Carol V. Robinson, Wei-Min Liu
Publikováno v:
SSRN Electronic Journal.
Protein glycosylation is a widespread post-translational modification. The first committed step to the lipid-linked glycan used for this process is catalysed by dolichyl-phosphate N-acetylglucosamine-phosphotransferase DPAGT1 (GPT/E.C. 2.7.8.15). Mis
Autor:
Matt Parton, Wei Wei Liu, Maryam Sedghi, Andrew M. Schaefer, Maria Elena Farrugia, Katsiaryna Belaya, Susan Maxwell, Jacqueline Palace, Hanns Lochmüller, Simon J. McGowan, Keivan Basiri, Anna Sarkozy, Wyatt W. Yue, Kate Bushby, Matthew Pitt, David Beeson, Richard E. Petty, Timothy J. Walls, Pedro M. Rodríguez Cruz, Marta Bertoli, Robin Kennett, Francesco Muntoni
Publikováno v:
Brain
Congenital myasthenic syndromes are associated with impairments in neuromuscular transmission. Belaya et al. show that mutations of the glycosylation pathway enzyme GMPPB, which has previously been implicated in muscular dystrophy dystroglycanopathy,
Publikováno v:
Neuromuscular Disorders
Mutations in DPAGT1 are a newly recognised cause of congenital myasthenic syndrome. DPAGT1 encodes an early component of the N-linked glycosylation pathway. Initially mutations in DPAGT1 have been associated with the onset of the severe multisystem d
Autor:
Katsiaryna Belaya, Wei Wei Liu, Sarah Finlayson, David Beeson, Judith Cossins, Jacqueline Palace, Susan Maxwell
Publikováno v:
Annals of the New York Academy of Sciences. 1275:29-35
Congenital myasthenic syndromes (CMS) are a group of inherited disorders that arise from impaired signal transmission at the neuromuscular synapse. They are characterized by fatigable muscle weakness. This is a heterogenous group of disorders with 15
Autor:
Angela Vincent, David Beeson, Judith Cossins, Inga Koneczny, Susan Maxwell, Patrick Waters, Maria Isabel Leite, Katarzyna Marta Zoltowska, Katsiaryna Belaya, Leslie Jacobson
Publikováno v:
Annals of the New York Academy of Sciences. 1275:123-128
Around 80% of myasthenia gravis patients have antibodies against the acetylcholine receptor, and 0-60% of the remaining patients have antibodies against the muscle-specific tyrosine kinase, MuSK. Another recently identified antigen is low-density lip
Autor:
Richard J. Butler, George Sirinakis, Uwe Irion, Dmitry Nashchekin, Katsiaryna Belaya, Vítor Trovisco, Jack J. Lee, Elizabeth R. Gavis, Daniel St Johnston
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1b2dfd3a4e41dab12482f295b5dc7d3
https://doi.org/10.7554/elife.17537.039
https://doi.org/10.7554/elife.17537.039