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Eric Legius

Showing results (51-60 of 165) with videos related to

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European Journal of Human Genetics : EJHG|January 24, 2008
Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletionsKatharina Steinmann, Lan Kluwe, David N Cooper, et al.
Breast Cancer Research and Treatment|April 14, 2007
Prophylactic mastectomy in familial breast carcinoma. What do the pathologic findings learn us?Karin Leunen, Maria Drijkoningen, Patrick Neven, et al.
Journal of Autism and Developmental Disorders|December 6, 2014
Autism spectrum disorder profile in neurofibromatosis type IShruti Garg, Ellen Plasschaert, Mie-Jef Descheemaeker, et al.
Molecular Autism|July 27, 2021
MEK inhibition ameliorates social behavior phenotypes in a Spred1 knockout mouse model for RASopathy disordersSarah C Borrie, Ellen Plasschaert, Zsuzsanna Callaerts-Vegh, et al.
Gynecologic and Obstetric Investigation|January 30, 2010
Has the prevalence of congenital abnormalities after intracytoplasmic sperm injection increased? The Leuven data 1994-2000 and a review of the literatureAn Hindryckx, Karen Peeraer, Sophie Debrock, et al.
Neurobiology of Disease|June 23, 2004
Genetic and phenotypic characterization of tumor cells derived from malignant peripheral nerve sheath tumors of neurofibromatosis type 1 patientsSilke Frahm, Victor-F Mautner, Hilde Brems, et al.
European Journal of Medical Genetics|March 23, 2010
Investigation of gene dosage imbalances in patients with Noonan syndrome using multiplex ligation-dependent probe amplification analysisAnna-Maja Nyström, Sara Ekvall, Ann-Charlotte Thuresson, et al.
European Journal of Human Genetics : EJHG|October 16, 2004
Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxiaHilde Van Esch, Rene Dom, Dorien Bex, et al.
Genes, Chromosomes & Cancer|May 16, 2012
Biallelic inactivation of NF1 in a sporadic plexiform neurofibromaEline Beert, Hilde Brems, Marleen Renard, et al.
The Journal of Biological Chemistry|December 5, 2015
Interaction between a Domain of the Negative Regulator of the Ras-ERK Pathway, SPRED1 Protein, and the GTPase-activating Protein-related Domain of Neurofibromin Is Implicated in Legius Syndrome and Neurofibromatosis Type 1Yasuko Hirata, Hilde Brems, Mayu Suzuki, et al.
Pageof 17

Showing results (51-60 of 165) with videos related to

Sort By:
Pageof 17
European Journal of Human Genetics : EJHG|January 24, 2008
Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletionsKatharina Steinmann, Lan Kluwe, David N Cooper, et al.
Breast Cancer Research and Treatment|April 14, 2007
Prophylactic mastectomy in familial breast carcinoma. What do the pathologic findings learn us?Karin Leunen, Maria Drijkoningen, Patrick Neven, et al.
Journal of Autism and Developmental Disorders|December 6, 2014
Autism spectrum disorder profile in neurofibromatosis type IShruti Garg, Ellen Plasschaert, Mie-Jef Descheemaeker, et al.
Molecular Autism|July 27, 2021
MEK inhibition ameliorates social behavior phenotypes in a Spred1 knockout mouse model for RASopathy disordersSarah C Borrie, Ellen Plasschaert, Zsuzsanna Callaerts-Vegh, et al.
Gynecologic and Obstetric Investigation|January 30, 2010
Has the prevalence of congenital abnormalities after intracytoplasmic sperm injection increased? The Leuven data 1994-2000 and a review of the literatureAn Hindryckx, Karen Peeraer, Sophie Debrock, et al.
Neurobiology of Disease|June 23, 2004
Genetic and phenotypic characterization of tumor cells derived from malignant peripheral nerve sheath tumors of neurofibromatosis type 1 patientsSilke Frahm, Victor-F Mautner, Hilde Brems, et al.
European Journal of Medical Genetics|March 23, 2010
Investigation of gene dosage imbalances in patients with Noonan syndrome using multiplex ligation-dependent probe amplification analysisAnna-Maja Nyström, Sara Ekvall, Ann-Charlotte Thuresson, et al.
European Journal of Human Genetics : EJHG|October 16, 2004
Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxiaHilde Van Esch, Rene Dom, Dorien Bex, et al.
Genes, Chromosomes & Cancer|May 16, 2012
Biallelic inactivation of NF1 in a sporadic plexiform neurofibromaEline Beert, Hilde Brems, Marleen Renard, et al.
The Journal of Biological Chemistry|December 5, 2015
Interaction between a Domain of the Negative Regulator of the Ras-ERK Pathway, SPRED1 Protein, and the GTPase-activating Protein-related Domain of Neurofibromin Is Implicated in Legius Syndrome and Neurofibromatosis Type 1Yasuko Hirata, Hilde Brems, Mayu Suzuki, et al.
Pageof 17