T G Thompson
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Explore the profile of T G Thompson including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
430
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Recent Articles
1.
Dalkilic I, Schienda J, Thompson T, Kunkel L
Mol Cell Biol
. 2006 Aug;
26(17):6522-34.
PMID: 16914736
FilaminC (FLNc) is the muscle-specific member of a family of actin binding proteins. Although it interacts with many proteins involved in muscular dystrophies, its unique role in muscle is poorly...
2.
Bonnemann C, Thompson T, van der Ven P, Goebel H, Warlo I, Vollmers B, et al.
J Neurol Sci
. 2002 Dec;
206(1):71-8.
PMID: 12480088
Filamin C is the muscle isoform of a group of large actin-crosslinking proteins. On the one hand, filamin C is associated with the Z-disk of the myofibrillar apparatus and binds...
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Mizuno Y, Thompson T, Guyon J, Lidov H, BROSIUS M, Imamura M, et al.
Proc Natl Acad Sci U S A
. 2001 May;
98(11):6156-61.
PMID: 11353857
Dystrobrevin is a component of the dystrophin-associated protein complex and has been shown to interact directly with dystrophin, alpha1-syntrophin, and the sarcoglycan complex. The precise role of alpha-dystrobrevin in skeletal...
7.
Takada F, Vander Woude D, Tong H, Thompson T, Watkins S, Kunkel L, et al.
Proc Natl Acad Sci U S A
. 2001 Feb;
98(4):1595-600.
PMID: 11171996
To better understand the structure and function of Z lines, we used sarcomeric isoforms of alpha-actinin and gamma-filamin to screen a human skeletal muscle cDNA library for interacting proteins by...
8.
Bonnemann C, Cox G, Shapiro F, Wu J, Feener C, Thompson T, et al.
Proc Natl Acad Sci U S A
. 2000 Feb;
97(3):1212-7.
PMID: 10655510
Multiple epiphyseal dysplasia (MED) is a degenerative cartilage condition shown in some cases to be caused by mutations in genes encoding cartilage oligomeric matrix protein or type IX collagen. We...
9.
Thompson T, Chan Y, Hack A, BROSIUS M, Rajala M, Lidov H, et al.
J Cell Biol
. 2000 Jan;
148(1):115-26.
PMID: 10629222
Mutations in genes encoding for the sarcoglycans, a subset of proteins within the dystrophin-glycoprotein complex, produce a limb-girdle muscular dystrophy phenotype; however, the precise role of this group of proteins...
10.
Scharf J, Endrizzi M, Wetter A, Huang S, Thompson T, Zerres K, et al.
Nat Genet
. 1998 Sep;
20(1):83-6.
PMID: 9731538
Spinal muscular atrophy (SMA) is a common recessive disorder characterized by the loss of lower motor neurons in the spinal cord. The disease has been classified into three types based...