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Susanna M I Goorden

Showing results (1-10 of 13) with videos related to

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Trends in Genetics : TIG|September 9, 2008
Oncogenes on my mind: ERK and MTOR signaling in cognitive diseasesLianne C Krab, Susanna M I Goorden, Ype Elgersma
Nederlands Tijdschrift Voor Geneeskunde|October 25, 2013
[Liver disorders in adults: ALT and AST]Susanna M I Goorden, Tineke E Buffart, Annemieke Bakker, et al.
Blood Advances|January 19, 2018
Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1Srinivas Aluri, Rongbao Zhao, Charlotte Lubout, et al.
Annals of Neurology|December 11, 2007
Cognitive deficits in Tsc1+/- mice in the absence of cerebral lesions and seizuresSusanna M I Goorden, Geeske M van Woerden, Louise van der Weerd, et al.
Human Molecular Genetics|March 12, 2015
Intact neuronal function in Rheb1 mutant mice: implications for TORC1-based treatmentsSusanna M I Goorden, Elisabeth Abs, Caroline F Bruinsma, et al.
Frontiers in Neurology|August 6, 2019
Biochemical Screening of Intellectually Disabled Patients: A Stepping Stone to Initiate a Newborn Screening Program in PakistanMuhammad Wasim, Haq Nawaz Khan, Hina Ayesha, et al.
Molecular and Cellular Biology|February 16, 2011
Rheb is essential for murine developmentSusanna M I Goorden, Marianne Hoogeveen-Westerveld, Caroline Cheng, et al.
Annals of Neurology|May 31, 2013
TORC1-dependent epilepsy caused by acute biallelic Tsc1 deletion in adult miceElisabeth Abs, Susanna M I Goorden, Jadwiga Schreiber, et al.
Pediatric Neurology|August 3, 2019
Successful Treatment of Hereditary Folate Malabsorption With Intramuscular Folinic AcidCharlotte M A Lubout, Susanna M I Goorden, Karin van den Hurk, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 22, 2014
Temporal and region-specific requirements of αCaMKII in spatial and contextual learningKatharina G Achterberg, Gabriëlle H S Buitendijk, Martijn J Kool, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Trends in Genetics : TIG|September 9, 2008
Oncogenes on my mind: ERK and MTOR signaling in cognitive diseasesLianne C Krab, Susanna M I Goorden, Ype Elgersma
Nederlands Tijdschrift Voor Geneeskunde|October 25, 2013
[Liver disorders in adults: ALT and AST]Susanna M I Goorden, Tineke E Buffart, Annemieke Bakker, et al.
Blood Advances|January 19, 2018
Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1Srinivas Aluri, Rongbao Zhao, Charlotte Lubout, et al.
Annals of Neurology|December 11, 2007
Cognitive deficits in Tsc1+/- mice in the absence of cerebral lesions and seizuresSusanna M I Goorden, Geeske M van Woerden, Louise van der Weerd, et al.
Human Molecular Genetics|March 12, 2015
Intact neuronal function in Rheb1 mutant mice: implications for TORC1-based treatmentsSusanna M I Goorden, Elisabeth Abs, Caroline F Bruinsma, et al.
Frontiers in Neurology|August 6, 2019
Biochemical Screening of Intellectually Disabled Patients: A Stepping Stone to Initiate a Newborn Screening Program in PakistanMuhammad Wasim, Haq Nawaz Khan, Hina Ayesha, et al.
Molecular and Cellular Biology|February 16, 2011
Rheb is essential for murine developmentSusanna M I Goorden, Marianne Hoogeveen-Westerveld, Caroline Cheng, et al.
Annals of Neurology|May 31, 2013
TORC1-dependent epilepsy caused by acute biallelic Tsc1 deletion in adult miceElisabeth Abs, Susanna M I Goorden, Jadwiga Schreiber, et al.
Pediatric Neurology|August 3, 2019
Successful Treatment of Hereditary Folate Malabsorption With Intramuscular Folinic AcidCharlotte M A Lubout, Susanna M I Goorden, Karin van den Hurk, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 22, 2014
Temporal and region-specific requirements of αCaMKII in spatial and contextual learningKatharina G Achterberg, Gabriëlle H S Buitendijk, Martijn J Kool, et al.
Pageof 2