Results
|
|
161.
|
|
|
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162.
|
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy. [electronic resource] by
- Nicole, Sophie
- Chaouch, Amina
- Torbergsen, Torberg
- Bauché, Stéphanie
- de Bruyckere, Elodie
- Fontenille, Marie-Joséphine
- Horn, Morten A
- van Ghelue, Marijke
- Løseth, Sissel
- Issop, Yasmin
- Cox, Daniel
- Müller, Juliane S
- Evangelista, Teresinha
- Stålberg, Erik
- Ioos, Christine
- Barois, Annie
- Brochier, Guy
- Sternberg, Damien
- Fournier, Emmanuel
- Hantaï, Daniel
- Abicht, Angela
- Dusl, Marina
- Laval, Steven H
- Griffin, Helen
- Eymard, Bruno
- Lochmüller, Hanns
Producer: 20141106
In:
Brain : a journal of neurology vol. 137
Availability: No items available.
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163.
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164.
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165.
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166.
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167.
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Zymogen activation of neurotrypsin and neurotrypsin-dependent agrin cleavage on the cell surface are enhanced by glycosaminoglycans. [electronic resource] by
- Gisler, Claudio
- Lüscher, Daniel
- Schätzle, Philipp
- Dürr, Stephanie
- Baici, Antonio
- Galliciotti, Giovanna
- Reif, Raymond
- Bolliger, Marc F
- Kunz, Beat
- Sonderegger, Peter
Producer: 20130820
In:
The Biochemical journal vol. 453
Availability: No items available.
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168.
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169.
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170.
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171.
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172.
|
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173.
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Detection of muscle wasting in patients with chronic heart failure using C-terminal agrin fragment: results from the Studies Investigating Co-morbidities Aggravating Heart Failure (SICA-HF). [electronic resource] by
- Steinbeck, Lisa
- Ebner, Nicole
- Valentova, Miroslava
- Bekfani, Tarek
- Elsner, Sebastian
- Dahinden, Pius
- Hettwer, Stefan
- Scherbakov, Nadja
- Schefold, Jörg C
- Sandek, Anja
- Springer, Jochen
- Doehner, Wolfram
- Anker, Stefan D
- von Haehling, Stephan
Producer: 20160926
In:
European journal of heart failure vol. 17
Availability: No items available.
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174.
|
|
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175.
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Novel SEA and LG2 Agrin mutations causing congenital Myasthenic syndrome. [electronic resource] by
- Xi, Jianying
- Yan, Chong
- Liu, Wei-Wei
- Qiao, Kai
- Lin, Jie
- Tian, Xia
- Wu, Hui
- Lu, Jiahong
- Wong, Lee-Jun
- Beeson, David
- Zhao, Chongbo
Producer: 20180904
In:
Orphanet journal of rare diseases vol. 12
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177.
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A mechanism in agrin signaling revealed by a prevalent Rapsyn mutation in congenital myasthenic syndrome. [electronic resource] by
- Xing, Guanglin
- Jing, Hongyang
- Zhang, Lei
- Cao, Yu
- Li, Lei
- Zhao, Kai
- Dong, Zhaoqi
- Chen, Wenbing
- Wang, Hongsheng
- Cao, Rangjuan
- Xiong, Wen-Cheng
- Mei, Lin
Producer: 20200131
In:
eLife vol. 8
Availability: No items available.
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