Results 61 to 70 of about 16,607 (189)

Genetic testing among patients evaluated for epilepsy surgery

open access: yesEpileptic Disorders, EarlyView.
Abstract Objective Genetic testing performed to identify the underlying etiology of epilepsy has become increasingly common and is now being recommended as part of the presurgical evaluation for epilepsy surgery. This study aimed to characterize the types of genetic tests performed in patients evaluated for epilepsy surgery and assess how genetic ...
Anni Saarela   +7 more
wiley   +1 more source

GEFS member 8

open access: yes
GEFS member 8 forecast for 30 May 2013 - 31 May ...
Putnam, Bryan
core   +1 more source

GEFS+ mutation affects sleep/wake behavior.

open access: yes, 2015
(A) The 24 hr activity profiles, (B) 12 hr LD activity counts, and (C) 24 hr sleep profiles of virgin females (☿), mated females (♀), and males (♂) for knock-in controls (n = 85, 93, 95) and GEFS+ mutants (n = 88, 87, 94).
Patrick Lansdon (794165)   +2 more
core   +1 more source

GEFs and GAPs: Critical Elements in the Control of Small G Proteins [PDF]

open access: yes, 2007
Guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs) regulate the activity of small guanine nucleotide-binding (G) proteins to control cellular functions.
Bos, J.   +8 more
core   +1 more source

The 164 K, 165 K, and 167 K residues of VP1 are vital for goose parvovirus proliferation in GEFs based on PCR-based reverse genetics system

open access: yesVirology Journal, 2019
Background Goose parvovirus (GPV) is the etiological agent of Derzsy’s disease and is fatal for gosling. Research on the molecular basis of GPV pathogenicity has been hampered by the lack of a reliable reverse genetics system.
Peng Liu   +18 more
doaj   +1 more source

Electroclinical phenotypes—genetic characterization of developmental and epileptic encephalopathies in a cohort study

open access: yesEpileptic Disorders, EarlyView.
Abstract Objective Developmental and epileptic encephalopathies (DEEs) are characterized by refractory seizures and frequently recurring epileptic activity with neurodevelopmental delay or regression that usually begin in early life. We aimed to define the relationship between electroclinical features and etiology, as well as the genotype–phenotype ...
Burcu Yaman   +7 more
wiley   +1 more source

Genetics of Febrile Seizures and Epilepsy (GEFS+)

open access: yes, 2008
Mutations in 3 genes SCN1A, SCN1B and GABRG2 have been shown to cause GEFS+ in families of various ethnic ...
J Gordon Millichap
core   +1 more source

Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation

open access: yesNeurobiology of Disease, 2020
Over 1250 mutations in SCN1A, the Nav1.1 voltage-gated sodium channel gene, are associated with seizure disorders including GEFS+. To evaluate how a specific mutation, independent of genetic background, causes seizure activity we generated two pairs of ...
Yunyao Xie   +7 more
doaj   +1 more source

Oligogenic inheritance in epilepsy: A systematic exome‐wide analysis

open access: yesEpilepsia, EarlyView.
Abstract Objective Genetic factors contribute to the majority of epilepsies, but the exact genetic cause remains unknown in most patients. Incomplete penetrance and variable expressivity are frequent, and recent studies showed a burden of deleterious variants in epilepsy genes, suggesting a role for oligogenic inheritance.
Sarah Duerinckx   +192 more
wiley   +1 more source

Rho GAPs and GEFs Controling switches in endothelial cell adhesion

open access: yes, 2014
Within blood vessels, endothelial cell-cell and cell-matrix adhesions are crucial to preserve barrier function, and these adhesions are tightly controlled during vascular development, angiogenesis, and transendothelial migration of inflammatory cells ...
van Buul, Jaap D   +3 more
core   +1 more source

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