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Norbert F Ajeawung

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

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Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|August 10, 2010
Translational applications of microRNA genes in medulloblastomasNorbert F Ajeawung, Ben Li, Deepak Kamnasaran
Cancer Letters|February 14, 2013
The microtubule binding drug EM011 inhibits the growth of paediatric low grade gliomasNorbert F Ajeawung, Harish C Joshi, Deepak Kamnasaran
Journal of Pediatric Oncology|April 22, 2014
Investigation of Targetin, a Microtubule Binding Agent which Regresses the Growth of Pediatric High and Low Grade GliomasNorbert F Ajeawung, Harish C Joshi, Deepak Kamnasaran
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|October 10, 2012
Advances in molecular targets for the treatment of medulloblastomasNorbert F Ajeawung, Hao Y Wang, Peter Gould, et al.
Journal of Pediatric Oncology|April 22, 2014
<i>In-Vitro</i> and <i>Ex-Vivo</i> Investigations of the Microtubule Binding Drug Targetin on AngiogenesisNorbert F Ajeawung, Lotta Mononen, Andrea Thorn, et al.
The American Journal of Pathology|June 28, 2011
NPAS3 demonstrates features of a tumor suppressive role in driving the progression of AstrocytomasFrederico Moreira, Tim-Rasmus Kiehl, Kelvin So, et al.
Frontiers in Neurology|August 28, 2020
Clinicopathological Relationships in an Aged Case of DOORS Syndrome With a p.Arg506X Mutation in the <i>ATP6V1B2</i> GeneDénes Zádori, Levente Szalárdy, Zita Reisz, et al.
American Journal of Human Genetics|July 16, 2019
Mutations in ANAPC1, Encoding a Scaffold Subunit of the Anaphase-Promoting Complex, Cause Rothmund-Thomson Syndrome Type 1Norbert F Ajeawung, Thi Tuyet Mai Nguyen, Linchao Lu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2020
DOORS syndrome and a recurrent truncating ATP6V1B2 variantEliane Beauregard-Lacroix, Guillermo Pacheco-Cuellar, Norbert F Ajeawung, et al.
European Journal of Human Genetics : EJHG|January 14, 2018
Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndromeJean-Luc Alessandri, Christopher T Gordon, Marie-Line Jacquemont, et al.
Pageof 2

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

Sort By:
Pageof 2
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|August 10, 2010
Translational applications of microRNA genes in medulloblastomasNorbert F Ajeawung, Ben Li, Deepak Kamnasaran
Cancer Letters|February 14, 2013
The microtubule binding drug EM011 inhibits the growth of paediatric low grade gliomasNorbert F Ajeawung, Harish C Joshi, Deepak Kamnasaran
Journal of Pediatric Oncology|April 22, 2014
Investigation of Targetin, a Microtubule Binding Agent which Regresses the Growth of Pediatric High and Low Grade GliomasNorbert F Ajeawung, Harish C Joshi, Deepak Kamnasaran
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|October 10, 2012
Advances in molecular targets for the treatment of medulloblastomasNorbert F Ajeawung, Hao Y Wang, Peter Gould, et al.
Journal of Pediatric Oncology|April 22, 2014
<i>In-Vitro</i> and <i>Ex-Vivo</i> Investigations of the Microtubule Binding Drug Targetin on AngiogenesisNorbert F Ajeawung, Lotta Mononen, Andrea Thorn, et al.
The American Journal of Pathology|June 28, 2011
NPAS3 demonstrates features of a tumor suppressive role in driving the progression of AstrocytomasFrederico Moreira, Tim-Rasmus Kiehl, Kelvin So, et al.
Frontiers in Neurology|August 28, 2020
Clinicopathological Relationships in an Aged Case of DOORS Syndrome With a p.Arg506X Mutation in the <i>ATP6V1B2</i> GeneDénes Zádori, Levente Szalárdy, Zita Reisz, et al.
American Journal of Human Genetics|July 16, 2019
Mutations in ANAPC1, Encoding a Scaffold Subunit of the Anaphase-Promoting Complex, Cause Rothmund-Thomson Syndrome Type 1Norbert F Ajeawung, Thi Tuyet Mai Nguyen, Linchao Lu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2020
DOORS syndrome and a recurrent truncating ATP6V1B2 variantEliane Beauregard-Lacroix, Guillermo Pacheco-Cuellar, Norbert F Ajeawung, et al.
European Journal of Human Genetics : EJHG|January 14, 2018
Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndromeJean-Luc Alessandri, Christopher T Gordon, Marie-Line Jacquemont, et al.
Pageof 2