Enhanced excitation-coupled Ca 2+ entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with central core disease

Author： Treves Susan   Vukcevic Mirko   Jeannet Pierre-Yves   Levano Soledad   Girard Thierry   Urwyler Albert   Fischer Dirk   Voit Thomas   Jungbluth Heinz   Lillis Sue   Muntoni Francesco   Quinlivan Ros   Sarkozy Anna   Bushby Kate   Zorzato Francesco  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.20, Iss.10, 2011-05, pp. : 2079-2079

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Enhanced excitation-coupled Ca 2 entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with central core disease

By Treves Susan   Vukcevic Mirko   Jeannet Pierre-Yves   Levano Soledad   Girard Thierry   Urwyler Albert   Fischer Dirk   Voit Thomas   Jungbluth Heinz   Lillis Sue   Muntoni Francesco   Quinlivan Ros   Sarkozy Anna   Bushby Kate   Zorzato Francesco  

Human Molecular Genetics, Vol. 20, Iss. 3, 2011-02 ,pp. : 589-600

Oxford University Press

Access to resources Recommend Favorite

Adenovirus-mediated transfer of the acid α-glucosidase gene into fibroblasts, myoblasts and myotubes from patients with glycogen storage disease type II leads to high level expression of enzyme and corrects glycogen accumulation

By Nicolino M.P.  

Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1695-1702

Oxford University Press

Access to resources Recommend Favorite

Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease

By Kong Xiao-Fei   Vogt Guillaume   Itan Yuval   Macura-Biegun Anna   Szaflarska Anna   Kowalczyk Danuta   Chapgier Ariane   Abhyankar Avinash   Furthner Dieter   Djambas Khayat Claudia   Okada Satoshi   Bryant Vanessa L.   Bogunovic Dusan   Kreins Alexandra   Moncada-Vélez Marcela   Migaud Mélanie   Al-Ajaji Sulaiman   Al-Muhsen Saleh   Holland Steven M.   Abel Laurent   Picard Capucine   Chaussabel Damien   Bustamante Jacinta   Casanova Jean-Laurent   Boisson-Dupuis Stéphanie  

Human Molecular Genetics, Vol. 22, Iss. 4, 2013-02 ,pp. : 769-781

Oxford University Press

Access to resources Recommend Favorite

A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation

By Babbs Christian   Heller Raoul   Everman David   Crocker Mark   Twigg Stephen   Schwartz Charles   Giele Henk   Wilkie Andrew  

Human Genetics, Vol. 122, Iss. 2, 2007-09 ,pp. : 191-199

Springer Publishing Company

Access to resources Recommend Favorite

Abnormal Ca 2+ release and catecholamine-induced arrhythmias in mitochondrial cardiomyopathy

By Tavi Pasi  

Human Molecular Genetics, Vol. 14, Iss. 8, 2005-04 ,pp. : 1069-1076

Oxford University Press

Access to resources Recommend Favorite