Zobrazeno 1 - 10
of 169
pro vyhledávání: '"K, KONIG"'
Autor:
Manu Tewari, Hansell H. Stedman, Leonard T. Su, Douglas R. Stewart, James M. Burkman, Eric Jullian, Joseph B. Shrager, Philippe R. Desjardins, Michael R. Rickels, Stephane K. Konig, Megha C. Shah, Neal A. Rubinstein, Rebecca Hoffman, Evelyn Bricklin
Publikováno v:
Journal of Muscle Research and Cell Motility. 21:345-355
Myosin heavy chain (MyHC) is the major contractile protein of muscle. We report the first complete cosmid cloning and definitive physical map of the tandemly linked human skeletal MyHC genes at 17p13.1. The map provides new information on the order,
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
CLEO '97., Summaries of Papers Presented at the Conference on Lasers and Electro-Optics.
Autor:
R. Cuzzilla, K. Konig
Publikováno v:
Early Human Development. 89:S79-S80
Autor:
Julie C. Fitzgerald, Hansell H. Stedman, James M. Burkman, Leonard T. Su, Marilyn A. Mitchell, Stephane K. Konig
Publikováno v:
The Journal of biological chemistry. 277(31)
The mammalian skeletal myosin heavy chain locus is composed of a six-membered family of tandemly linked genes whose complex regulation plays a central role in striated muscle development and diversification. We have used publicly available genomic DN
Autor:
J B, Shrager, P R, Desjardins, J M, Burkman, S K, Konig, S K, Stewart, L, Su, M C, Shah, E, Bricklin, M, Tewari, R, Hoffman, M R, Rickels, E H, Jullian, N A, Rubinstein, H H, Stedman
Publikováno v:
Journal of muscle research and cell motility. 21(4)
Myosin heavy chain (MyHC) is the major contractile protein of muscle. We report the first complete cosmid cloning and definitive physical map of the tandemly linked human skeletal MyHC genes at 17p13.1. The map provides new information on the order,
Autor:
Leonard T. Su, James M. Wilson, Stephane K. Konig, Edward B. Lankford, Philippe R. Desjardins, Marilyn A. Mitchell, James P. Greelish, Guangping Gao, Xiang guang Zheng, James M. Burkman, Isabelle Mercier, Hansell H. Stedman, John Leferovich, Haiyan Chen, Rita J. Balice-Gordon
Publikováno v:
ResearcherID
Limb-girdle muscular dystrophies 2C-F represent a family of autosomal recessive diseases caused by defects in sarcoglycan genes. The cardiomyopathic hamster is a naturally occurring model for limb-girdle muscular dystrophy caused by a primary deficie
Publikováno v:
Transplantation proceedings. 26(4)
Publikováno v:
Transplantation proceedings. 26(3)
Publikováno v:
Zeitschrift für Chemie. 6:271-271