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Nature Structural Biology
|
February 27, 2001
Prediction and confirmation of a site critical for effector regulation of RGS domain activity
M E Sowa, W He, K C Slep, et al.
Science (New York, N.Y.)
|
January 17, 1997
Receptor and betagamma binding sites in the alpha subunit of the retinal G protein transducin
R Onrust, P Herzmark, P Chi, et al.
The Journal of Biological Chemistry
|
June 8, 1999
Similar structures and shared switch mechanisms of the beta2-adrenoceptor and the parathyroid hormone receptor. Zn(II) bridges between helices III and VI block activation
S P Sheikh, J P Vilardarga, T J Baranski, et al.
The Journal of Biological Chemistry
|
May 21, 1999
C5a receptor activation. Genetic identification of critical residues in four transmembrane helices
T J Baranski, P Herzmark, O Lichtarge, et al.
Annals of Neurology
|
May 11, 2000
Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes
R E Amir, I B Van den Veyver, R Schultz, et al.
Page
of 3
Search research articles
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Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
Nature Structural Biology
|
February 27, 2001
Prediction and confirmation of a site critical for effector regulation of RGS domain activity
M E Sowa, W He, K C Slep, et al.
Science (New York, N.Y.)
|
January 17, 1997
Receptor and betagamma binding sites in the alpha subunit of the retinal G protein transducin
R Onrust, P Herzmark, P Chi, et al.
The Journal of Biological Chemistry
|
June 8, 1999
Similar structures and shared switch mechanisms of the beta2-adrenoceptor and the parathyroid hormone receptor. Zn(II) bridges between helices III and VI block activation
S P Sheikh, J P Vilardarga, T J Baranski, et al.
The Journal of Biological Chemistry
|
May 21, 1999
C5a receptor activation. Genetic identification of critical residues in four transmembrane helices
T J Baranski, P Herzmark, O Lichtarge, et al.
Annals of Neurology
|
May 11, 2000
Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes
R E Amir, I B Van den Veyver, R Schultz, et al.
Page
of 3