Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Fengqing Xiang"'
Autor:
Montse Olivé, Martin Engvall, Gianina Ravenscroft, Macarena Cabrera-Serrano, Hong Jiao, Carlo Augusto Bortolotti, Marcello Pignataro, Matteo Lambrughi, Haibo Jiang, Alistair R. R. Forrest, Núria Benseny-Cases, Stefan Hofbauer, Christian Obinger, Gianantonio Battistuzzi, Marzia Bellei, Marco Borsari, Giulia Di Rocco, Helena M. Viola, Livia C. Hool, Josep Cladera, Kristina Lagerstedt-Robinson, Fengqing Xiang, Anna Wredenberg, Francesc Miralles, Juan José Baiges, Edoardo Malfatti, Norma B. Romero, Nathalie Streichenberger, Christophe Vial, Kristl G. Claeys, Chiara S. M. Straathof, An Goris, Christoph Freyer, Martin Lammens, Guillaume Bassez, Juha Kere, Paula Clemente, Thomas Sejersen, Bjarne Udd, Noemí Vidal, Isidre Ferrer, Lars Edström, Anna Wedell, Nigel G. Laing
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
Myoglobin is a hemeprotein that reversibly binds oxygen and gives muscle its red color. Here, the authors report a genetic variant in the MB gene that associates with myoglobinopathy, an autosomal dominant progressive myopathy, and altered oxygen bin
Externí odkaz:
https://doaj.org/article/66b676bb69fb44be94c22654e712d730
Autor:
Caroline Ran, Karin Wirdefeldt, Lovisa Brodin, Mehrafarin Ramezani, Marie Westerlund, Fengqing Xiang, Anna Anvret, Thomas Willows, Olof Sydow, Anders Johansson, Dagmar Galter, Per Svenningsson, Andrea Carmine Belin
Publikováno v:
Parkinson's Disease, Vol 2017 (2017)
Nuclear factor erythroid 2-like 2 (NRF2) encodes a transcription factor regulating mechanisms of cellular protection and is activated by oxidative stress. NRF2 has therefore been hypothesized to confer protection against Parkinson’s disease and so
Externí odkaz:
https://doaj.org/article/e7dbcf9dd3ef4e7a865416f7baddc886
Autor:
Norma B. Romero, Nathalie Streichenberger, Kristina Lagerstedt-Robinson, Anna Wredenberg, Gianina Ravenscroft, Gianantonio Battistuzzi, Martin Lammens, Chiara S. M. Straathof, Martin Engvall, Christophe Vial, Haibo Jiang, Marzia Bellei, Marco Borsari, Fengqing Xiang, Juha Kere, Giulia Di Rocco, Helena M. Viola, Núria Benseny-Cases, Edoardo Malfatti, Nigel G. Laing, Bjarne Udd, Juan José Baiges, Lars Edström, Thomas Sejersen, Carlo Augusto Bortolotti, Marcello Pignataro, Noemi Vidal, Paula Clemente, Anna Wedell, Alistair R. R. Forrest, Stefan Hofbauer, Kristl G. Claeys, An Goris, Macarena Cabrera-Serrano, Matteo Lambrughi, Francesc Miralles, Montse Olivé, Christian Obinger, Isidre Ferrer, Livia C. Hool, Christoph Freyer, Guillaume Bassez, Hong Jiao, Josep Cladera
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Digital.CSIC. Repositorio Institucional del CSIC
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
Nature Communications
Nature Communications, Nature Publishing Group, 2019, 10, pp.1396. ⟨10.1038/s41467-019-09111-2⟩
Nature communications
Nature Communications, 2019, 10, pp.1396. ⟨10.1038/s41467-019-09111-2⟩
Nature Communications, 10
Universitat Autònoma de Barcelona
Digital.CSIC. Repositorio Institucional del CSIC
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
Nature Communications
Nature Communications, Nature Publishing Group, 2019, 10, pp.1396. ⟨10.1038/s41467-019-09111-2⟩
Nature communications
Nature Communications, 2019, 10, pp.1396. ⟨10.1038/s41467-019-09111-2⟩
Nature Communications, 10
Myoglobin, encoded by MB, is a small cytoplasmic globular hemoprotein highly expressed in cardiac myocytes and oxidative skeletal myofibers. Myoglobin binds O-2, facilitates its intracellular transport and serves as a controller of nitric oxide and r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c74251213720f9eb4140e00970a3dea
https://ddd.uab.cat/record/222847
https://ddd.uab.cat/record/222847
Autor:
Olof Sydow, Karin Wirdefeldt, Fengqing Xiang, Caroline Ran, Rawand Naiel Mehdi, Hans Nissbrandt, Andrea Carmine Belin, Camilla Fardell
Publikováno v:
The Open Neurology Journal
Background:Integrin alpha 8 (ITGA8) encodes the alpha 8 subunit of the integrin alpha8beta1 protein and has recently been suggested as a new candidate gene for Parkinson’s disease, an age related neurodegenerative disease with unknown etiology. ITG
Autor:
Anna Anvret, Olof Sydow, Andrea Carmine Belin, L.-A. Brodin, Marie Westerlund, Karin Wirdefeldt, Anders Johansson, Per Svenningsson, Fengqing Xiang, Thomas Willows, Caroline Ran, Mehrafarin Ramezani, Dagmar Galter
Publikováno v:
Parkinson's Disease, Vol 2017 (2017)
Parkinson's Disease
Parkinson's Disease
Nuclear factor erythroid 2-like 2 (NRF2) encodes a transcription factor regulating mechanisms of cellular protection and is activated by oxidative stress. NRF2 has therefore been hypothesized to confer protection against Parkinson’s disease and so
Autor:
Jakob Kristensen, Fengqing Xiang, Anna Vihola, Thomas Sejersen, Mathias Gautel, Sylvie Marchand, Gereon Franzen, Elisabeth Ehler, Lars Edström, Elena Rostkova, Birgit Brandmeier, Bjarne Udd, Stephan Lange, Isabelle Richard, Lars-Gunnar Gunnarsson, Birgitta Hedberg, Peter Hackman, Andrey Yakovenko, Simon M. Hughes
Publikováno v:
Science. 308:1599-1603
The giant sarcomeric protein titin contains a protein kinase domain (TK) ideally positioned to sense mechanical load. We identified a signaling complex where TK interacts with the zinc-finger protein nbr1 through a mechanically inducible conformation
Autor:
Bjarne Udd, Bruno Eymard, Rosaline Quinlivan, Giorgio Tasca, Taneli Raivio, Lars Edström, Ibrahim Mahjneh, Anni Evilä, Maxwell S. Damian, Fiona Norwood, Frédéric Chevessier, Rolf Schröder, Caroline Sewry, Françoise Chapon, Andoni Echaniz-Laguna, Johanna Palmio, Fengqing Xiang, Jocelyn Laporte, Anders Oldfors, Andrés Berardo, Peter Hackman, Ana Lia Taratuto, Mikko Kärppä, Philipp Gölitz, Matthias Tuerk, Johanna Tommiska, Pascal Laforêt, Jose Antonio Bueri, Carola Hedberg, Björn Brådvik
Publikováno v:
Journal of Neurology, Neurosurgery and Psychiatry; 85(3), pp 345-353 (2014)
Objective: Several families with characteristic features of hereditary myopathy with early respiratory failure (HMERF) have remained without genetic cause. This international study was initiated to clarify epidemiology and the genetic underlying caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ad8ad10a4331ae3127102355335c445
https://lup.lub.lu.se/record/4417638
https://lup.lub.lu.se/record/4417638
Autor:
Per Svenningsson, Martin Paucar, Fengqing Xiang, Ruth H Walker, Richard Moore, Elisabeth Winnberg
Publikováno v:
Prion. 7(6)
A minority of inherited prion diseases (IPD) are caused by four to 12 extra octapeptide repeat insertions (OPRI) in the prion protein gene (PRNP). Only four families affected by IPD with 8-OPRI have been reported, one of them was a three-generation S
Publikováno v:
Karolinska Institutet
We recently mapped a locus for a new variant of autosomal dominant myopathy (Swedish families) with proximal muscle weakness, early respiratory muscle involvement, and unique muscle biopsy findings to chromosomal region 2q24-31. In this study, a Fren
Autor:
Pereira Joseluiz, Angus John Clarke, Lars Edström, Naidu Sakkubai, Ingo Hansmann, Maria Anvret, Fengqing Xiang, Zhiping Zhang, Budden Sarojini, C. D. DeLozier-Blanchet
Publikováno v:
Karolinska Institutet
Rett syndrome (RS) is a disease of neurological development. First reported 30 years ago in 1966, its biological and genetic basis remains obscure. RS is commonly thought of as an X linked dominant disorder lethal to hemizygous males. The few familia