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Showing results (1171-1180 of 1,377) with videos related to

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Annals of Neurology|July 21, 2021
Postictal Psychosis in Epilepsy: A Clinicogenetic StudyVera Braatz, Helena Martins Custodio, Costin Leu, et al.
Epilepsia|July 16, 2015
Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsyDennis Lal, Katharina Pernhorst, Karl Martin Klein, et al.
Oncogene|November 21, 1998
Characterization of the mouse Men1 gene and its expression during developmentC Stewart, F Parente, F Piehl, et al.
Brain : a Journal of Neurology|March 20, 2012
KIAA1797/FOCAD encodes a novel focal adhesion protein with tumour suppressor function in gliomasAntje Brockschmidt, Detlef Trost, Heike Peterziel, et al.
Journal of Neurology|January 10, 2013
PRRT2-related disorders: further PKD and ICCA cases and review of the literatureFelicitas Becker, Julian Schubert, Pasquale Striano, et al.
Mucosal Immunology|February 2, 2025
Microbial remodeling of gut tryptophan metabolism and indole-3-lactate production regulate epithelial barrier repair and viral suppression in human and simian immunodeficiency virus infectionsClarissa Santos Rocha, Katie L Alexander, Carolina Herrera, et al.
Ebiomedicine|September 11, 2022
Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsiesJohanna Krüger, Julian Schubert, Josua Kegele, et al.
Acta Neuropathologica|April 30, 2021
Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial originAlisa Förster, Frank Brand, Rouzbeh Banan, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidismB T Teh, S Kytölä, F Farnebo, et al.
Epilepsia|January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsyDennis Lal, Holger Trucks, Rikke S Møller, et al.
Pageof 138

Showing results (1171-1180 of 1,377) with videos related to

Sort By:
Pageof 138
Annals of Neurology|July 21, 2021
Postictal Psychosis in Epilepsy: A Clinicogenetic StudyVera Braatz, Helena Martins Custodio, Costin Leu, et al.
Epilepsia|July 16, 2015
Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsyDennis Lal, Katharina Pernhorst, Karl Martin Klein, et al.
Oncogene|November 21, 1998
Characterization of the mouse Men1 gene and its expression during developmentC Stewart, F Parente, F Piehl, et al.
Brain : a Journal of Neurology|March 20, 2012
KIAA1797/FOCAD encodes a novel focal adhesion protein with tumour suppressor function in gliomasAntje Brockschmidt, Detlef Trost, Heike Peterziel, et al.
Journal of Neurology|January 10, 2013
PRRT2-related disorders: further PKD and ICCA cases and review of the literatureFelicitas Becker, Julian Schubert, Pasquale Striano, et al.
Mucosal Immunology|February 2, 2025
Microbial remodeling of gut tryptophan metabolism and indole-3-lactate production regulate epithelial barrier repair and viral suppression in human and simian immunodeficiency virus infectionsClarissa Santos Rocha, Katie L Alexander, Carolina Herrera, et al.
Ebiomedicine|September 11, 2022
Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsiesJohanna Krüger, Julian Schubert, Josua Kegele, et al.
Acta Neuropathologica|April 30, 2021
Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial originAlisa Förster, Frank Brand, Rouzbeh Banan, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidismB T Teh, S Kytölä, F Farnebo, et al.
Epilepsia|January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsyDennis Lal, Holger Trucks, Rikke S Møller, et al.
Pageof 138