Results
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3081.
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3082.
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3083.
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3084.
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Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers. [electronic resource] by
- Berge, K E
- Haugaa, K H
- Früh, A
- Anfinsen, O-G
- Gjesdal, K
- Siem, G
- Oyen, N
- Greve, G
- Carlsson, A
- Rognum, T O
- Hallerud, M
- Kongsgård, E
- Amlie, J P
- Leren, T P
Producer: 20090219
In:
Scandinavian journal of clinical and laboratory investigation vol. 68
Availability: No items available.
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3085.
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3086.
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3087.
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3088.
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3089.
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3090.
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3091.
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3092.
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3093.
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3094.
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3095.
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3096.
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3097.
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Structural insights into Ca(2+)-activated long-range allosteric channel gating of RyR1. [electronic resource] by
- Wei, Risheng
- Wang, Xue
- Zhang, Yan
- Mukherjee, Saptarshi
- Zhang, Lei
- Chen, Qiang
- Huang, Xinrui
- Jing, Shan
- Liu, Congcong
- Li, Shuang
- Wang, Guangyu
- Xu, Yaofang
- Zhu, Sujie
- Williams, Alan J
- Sun, Fei
- Yin, Chang-Cheng
Producer: 20171211
In:
Cell research vol. 26
Availability: No items available.
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3098.
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Calmodulin inhibition of human RyR2 channels requires phosphorylation of RyR2-S2808 or RyR2-S2814. [electronic resource] by
- Walweel, Kafa
- Gomez-Hurtado, Nieves
- Rebbeck, Robyn T
- Oo, Ye Wint
- Beard, Nicole A
- Molenaar, Peter
- Dos Remedios, Cris
- van Helden, Dirk F
- Cornea, Razvan L
- Knollmann, Björn C
- Laver, Derek R
Producer: 20200617
In:
Journal of molecular and cellular cardiology vol. 130
Availability: No items available.
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3099.
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3100.
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