Bilaketaren emaitzak - Fengqing Xiang
- Erakusten 1 - 5 emaitzak -- 5
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1
Mutation screening in Rett syndrome patients nork Fengqing Xiang
Argitaratua 2000Artigo -
2
Huntington Disease Phenocopy Is a Familial Prion Disease nork Richard C. Moore, Fengqing Xiang, Jeffrey Monaghan, Dong Han, Zhiping Zhang, Lars Edström, Maria Anvret, Stanley B. Prusiner
Argitaratua 2001Artigo -
3
The Kinase Domain of Titin Controls Muscle Gene Expression and Protein Turnover nork Stephan Lange, Fengqing Xiang, Andrey R Yakovenko, Anna Vihola, Peter Hackman, Elena Rostkova, Jakob Kristensen, Birgit Brandmeier, Gereon Franzen, Birgitta Hedberg, Lars Gunnarsson, Simon M. Hughes, Sylvie Marchand, Thomas Sejersen, Isabelle Richard, Lars Edström, Elisabeth Ehler, Bjarne Udd, Mathias Gautel
Argitaratua 2005Artigo -
4
Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden nork Caroline Ran, Lovisa Brodin, Lars Forsgren, Marie Westerlund, Mehrafarin Ramezani, Sandra Gellhaar, Fengqing Xiang, Camilla Fardell, Hans Nissbrandt, Peter Söderkvist, Andreas Puschmann, Emil Ygland, Lar̀s Olson, Thomas Willows, Anders Johansson, Olof Sydow, Karin Wirdefeldt, Dagmar Galter, Per Svenningsson, Andrea Carmine Belin
Argitaratua 2016Artigo -
5
Hereditary myopathy with early respiratory failure: occurrence in various populations nork Johanna Palmio, Anni Evilä, Françoise Chapon, Giorgio Tasca, Fengqing Xiang, Björn Brådvik, B. Eymard, Andoni Echaniz‐Laguna, Jocelyn Laporte, Mikko Kärppä, I. Mahjneh, Rosaline C. M. Quinlivan, Pascal Laforêt, Maxwell S. Damian, Andrés Berardo, A.L. Taratuto, J. A. Bueri, Johanna Tommiska, Taneli Raivio, Melanie J. Tuerk, Philipp Gölitz, Frédéric Chevessier, Caroline A. Sewry, F. Norwood, Carola Hedberg, Rolf Schröder, Lars Edström, Anders Oldfors, Peter Hackman, Bjarne Udd
Argitaratua 2013Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
Biology
Gene
Genetics
Medicine
Mutation
Disease
Genotype
Internal medicine
Mutant
Myocyte
Pathology
Sarcomere
Titin
Allele
Bioinformatics
Biopsy
Case-control study
Cell biology
Chemistry
Confidence interval
Etiology
Exome sequencing
Fatal familial insomnia
Genetic association
Genetic predisposition
Genotyping
Glucocerebrosidase
Huntingtin
Huntington's disease
LRRK2