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The Journal of Biological Chemistry
|
March 27, 2014
Divergent transducer-specific molecular efficacies generate biased agonism at a G protein-coupled receptor (GPCR)
Ryan T Strachan, Jin-peng Sun, David H Rominger, et al.
Human Molecular Genetics
|
April 6, 2000
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome
M Clement-Jones, S Schiller, E Rao, et al.
Mechanisms of Development
|
March 8, 2000
SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development
N A Hanley, D M Hagan, M Clement-Jones, et al.
Journal of Medicinal Chemistry
|
February 23, 2022
Structure-Based Design of a Chemical Probe Set for the 5-HT<sub>5A</sub> Serotonin Receptor
Anat Levit Kaplan, Ryan T Strachan, Joao M Braz, et al.
Nature Genetics
|
October 15, 1998
Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse
D Morgan, L Turnpenny, J Goodship, et al.
Journal of Medical Genetics
|
February 1, 1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families
M R Passos-Bueno, E S Moreira, S K Marie, et al.
Nature Chemical Biology
|
May 6, 2020
TRUPATH, an open-source biosensor platform for interrogating the GPCR transducerome
Reid H J Olsen, Jeffrey F DiBerto, Justin G English, et al.
Genomics
|
November 5, 1997
A sequence-ready physical map of a region of 12q24.1
B Renault, A Hovnanian, S Bryce, et al.
British Journal of Pharmacology
|
October 22, 2011
Chronic treatment in vivo with β-adrenoceptor agonists induces dysfunction of airway β(2) -adrenoceptors and exacerbates lung inflammation in mice
Rui Lin, Simone Degan, Barbara S Theriot, et al.
Human Molecular Genetics
|
April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump
R Sudbrak, J Brown, C Dobson-Stone, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 138) with videos related to
Sort By:
Page
of 14
The Journal of Biological Chemistry
|
March 27, 2014
Divergent transducer-specific molecular efficacies generate biased agonism at a G protein-coupled receptor (GPCR)
Ryan T Strachan, Jin-peng Sun, David H Rominger, et al.
Human Molecular Genetics
|
April 6, 2000
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome
M Clement-Jones, S Schiller, E Rao, et al.
Mechanisms of Development
|
March 8, 2000
SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development
N A Hanley, D M Hagan, M Clement-Jones, et al.
Journal of Medicinal Chemistry
|
February 23, 2022
Structure-Based Design of a Chemical Probe Set for the 5-HT<sub>5A</sub> Serotonin Receptor
Anat Levit Kaplan, Ryan T Strachan, Joao M Braz, et al.
Nature Genetics
|
October 15, 1998
Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse
D Morgan, L Turnpenny, J Goodship, et al.
Journal of Medical Genetics
|
February 1, 1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families
M R Passos-Bueno, E S Moreira, S K Marie, et al.
Nature Chemical Biology
|
May 6, 2020
TRUPATH, an open-source biosensor platform for interrogating the GPCR transducerome
Reid H J Olsen, Jeffrey F DiBerto, Justin G English, et al.
Genomics
|
November 5, 1997
A sequence-ready physical map of a region of 12q24.1
B Renault, A Hovnanian, S Bryce, et al.
British Journal of Pharmacology
|
October 22, 2011
Chronic treatment in vivo with β-adrenoceptor agonists induces dysfunction of airway β(2) -adrenoceptors and exacerbates lung inflammation in mice
Rui Lin, Simone Degan, Barbara S Theriot, et al.
Human Molecular Genetics
|
April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump
R Sudbrak, J Brown, C Dobson-Stone, et al.
Page
of 14