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Eric Legius

Showing results (61-70 of 165) with videos related to

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Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|June 19, 2016
Recurrent multilocular mandibular giant cell granuloma in neurofibromatosis type 1: Evidence for second hit mutation of NF1 gene in the jaw lesion and treatment with curettage and bone substitute materialsReinhard E Friedrich, Tobias J Grob, Silke Hollants, et al.
Gastroenterology|November 8, 2006
Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRAThomas de Raedt, Jan Cools, Maria Debiec-Rychter, et al.
Pediatric Dermatology|July 15, 2020
Keratinocytic epidermal nevi associated with localized fibro-osseous lesions without hypophosphatemiaLien Mestach, Satyamaanasa Polubothu, Alistair Calder, et al.
The Journal of Clinical Investigation|May 10, 2016
Cotargeting MNK and MEK kinases induces the regression of NF1-mutant cancersRebecca Lock, Rachel Ingraham, Ophélia Maertens, et al.
European Journal of Human Genetics : EJHG|November 24, 2011
Exploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromasLaura Thomas, Gill Spurlock, Claire Eudall, et al.
Genes, Chromosomes & Cancer|January 18, 2012
Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type 1-associated glomus tumorsDouglas R Stewart, Alexander Pemov, Peter Van Loo, et al.
Plos Genetics|September 7, 2013
Comparative oncogenomic analysis of copy number alterations in human and zebrafish tumors enables cancer driver discoveryGuangJun Zhang, Sebastian Hoersch, Adam Amsterdam, et al.
Genes, Chromosomes & Cancer|May 1, 2013
Multiple pilomatricomas with somatic CTNNB1 mutations in children with constitutive mismatch repair deficiencyMagdalena Chmara, Annekatrin Wernstedt, Bartosz Wasag, et al.
Journal of Medical Genetics|June 10, 2010
Diagnosis, management, and complications of glomus tumours of the digits in neurofibromatosis type 1Douglas R Stewart, Jennifer L Sloan, Lawrence Yao, et al.
Journal of Medical Genetics|June 2, 2024
Encephalocraniocutaneous lipomatosis phenotype associated with mosaic biallelic pathogenic variants in the <i>NF1</i> geneSteven Smeijers, Hilde Brems, Alexander Verhaeghe, et al.
Pageof 17

Showing results (61-70 of 165) with videos related to

Sort By:
Pageof 17
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|June 19, 2016
Recurrent multilocular mandibular giant cell granuloma in neurofibromatosis type 1: Evidence for second hit mutation of NF1 gene in the jaw lesion and treatment with curettage and bone substitute materialsReinhard E Friedrich, Tobias J Grob, Silke Hollants, et al.
Gastroenterology|November 8, 2006
Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRAThomas de Raedt, Jan Cools, Maria Debiec-Rychter, et al.
Pediatric Dermatology|July 15, 2020
Keratinocytic epidermal nevi associated with localized fibro-osseous lesions without hypophosphatemiaLien Mestach, Satyamaanasa Polubothu, Alistair Calder, et al.
The Journal of Clinical Investigation|May 10, 2016
Cotargeting MNK and MEK kinases induces the regression of NF1-mutant cancersRebecca Lock, Rachel Ingraham, Ophélia Maertens, et al.
European Journal of Human Genetics : EJHG|November 24, 2011
Exploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromasLaura Thomas, Gill Spurlock, Claire Eudall, et al.
Genes, Chromosomes & Cancer|January 18, 2012
Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type 1-associated glomus tumorsDouglas R Stewart, Alexander Pemov, Peter Van Loo, et al.
Plos Genetics|September 7, 2013
Comparative oncogenomic analysis of copy number alterations in human and zebrafish tumors enables cancer driver discoveryGuangJun Zhang, Sebastian Hoersch, Adam Amsterdam, et al.
Genes, Chromosomes & Cancer|May 1, 2013
Multiple pilomatricomas with somatic CTNNB1 mutations in children with constitutive mismatch repair deficiencyMagdalena Chmara, Annekatrin Wernstedt, Bartosz Wasag, et al.
Journal of Medical Genetics|June 10, 2010
Diagnosis, management, and complications of glomus tumours of the digits in neurofibromatosis type 1Douglas R Stewart, Jennifer L Sloan, Lawrence Yao, et al.
Journal of Medical Genetics|June 2, 2024
Encephalocraniocutaneous lipomatosis phenotype associated with mosaic biallelic pathogenic variants in the <i>NF1</i> geneSteven Smeijers, Hilde Brems, Alexander Verhaeghe, et al.
Pageof 17