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Showing 1-9 of 9 results for "SAB4200731" within Papers
Elisa Savino et al.
Cells, 10(10) (2021-10-24)
Mutations in the PRRT2 gene are the main cause for a group of paroxysmal neurological diseases including paroxysmal kinesigenic dyskinesia, episodic ataxia, benign familial infantile seizures, and hemiplegic migraine. In the mature central nervous system, the protein has both a
Structure and function of the N-cadherin/catenin complex in retinoblastoma
Van A, et al.
Investigative Ophthalmology & Visual Science, 43(3), 595-602 (2002)
Structure and biochemistry of cadherins and catenins
Shapiro L and Weis WI
Cold Spring Harbor Perspectives in Biology, a003053-a003053 (2009)
Apoptosis-related factors p53, bcl-2 and the defects of force transmission in dilated cardiomyopathy
Tsipis A , et al.
Pathology Research and Practice, 206(9), 625-630 (2010)
Structure-function analysis of cell adhesion by neural (N-) cadherin
Tamura K, et al.
Neuron, 20(6), 1153-1163 (1998)
Cadherin superfamily genes: functions, genomic organization, and neurologic diversity.
T Yagi et al.
Genes & development, 14(10), 1169-1180 (2000-05-19)
Molecular modification of N-cadherin in response to synaptic activity
Tanaka H, et al.
Neuron, 25(1), 93-107 (2000)
Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes
Moya P , et al.
European Journal of Human Genetics, 21(8), 850-850 (2013)
N-cadherin-mediated cell-cell adhesion promotes cell migration in a three-dimensional matrix
Shih W and Yamada S
Journal of Cell Science, 43(3), jcs-103861 (2012)
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