|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Macrothrombocytopenia and developmental delay with a de novo CDC42 mutation: Yet another locus for thrombocytopenia and developmental delay.
|
26386261 |
2015 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Characterization of a Cdc42 protein inhibitor and its use as a molecular probe.
|
23382385 |
2013 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Dual lipidation of the brain-specific Cdc42 isoform regulates its functional properties.
|
24059268 |
2013 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Expression analysis of Cdc42 in lung cancer and modulation of its expression by curcumin in lung cancer cell lines.
|
22266952 |
2012 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Cdc42 in oncogenic transformation, invasion, and tumorigenesis.
|
21515363 |
2011 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Local, persistent activation of Rho GTPases during plasticity of single dendritic spines.
|
21423166 |
2011 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Cdc42 and vesicle trafficking in polarized cells.
|
20633244 |
2010 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
RHO GTPase signaling for axon extension: is prenylation important?
|
20878268 |
2010 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Kainic acid-induced F-344 rat model of mesial temporal lobe epilepsy: gene expression and canonical pathways.
|
19700661 |
2009 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Molecular basis of dendritic arborization.
|
18511961 |
2008 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Neural palmitoyl-proteomics reveals dynamic synaptic palmitoylation.
|
19092927 |
2008 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
|
18245432 |
2008 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Involvement of E-cadherin, beta-catenin, Cdc42 and CXCR4 in the progression and prognosis of cutaneous melanoma.
|
17970806 |
2007 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Monosomy 1p36 deletion syndrome.
|
17918734 |
2007 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
GEFs and GAPs: critical elements in the control of small G proteins.
|
17540168 |
2007 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Cdc42 deficiency causes Sonic hedgehog-independent holoprosencephaly.
|
17050694 |
2006 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Rho GTPases and actin dynamics in membrane protrusions and vesicle trafficking.
|
16949823 |
2006 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Rho GTPases, dendritic structure, and mental retardation.
|
15884002 |
2005 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Overexpression of RhoA, Rac1, and Cdc42 GTPases is associated with progression in testicular cancer.
|
15269155 |
2004 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Structural basis of the Rho GTPase signaling.
|
14561717 |
2003 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.
|
12915473 |
2003 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome.
|
12687501 |
2003 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
The evolutionary history of effectors downstream of Cdc42 and Rac.
|
11864373 |
2002 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
Rho GTPases in cell biology.
|
12478284 |
2002 |
|
Multiple congenital anomalies
|
|
0.700 |
CausalMutation
|
CLINVAR |
The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation.
|
12195014 |
2002 |