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Najim Ameziane

Showing results (1-10 of 46) with videos related to

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The Turkish Journal of Pediatrics|December 25, 2015
Molecular diagnosis of Fanconi anemia with next-generation sequencing in a case with subtle signs and a negative chromosomal breakage testDeniz Aslan, Najim Ameziane, Johan P De Winter
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 26, 2023
Clonal and "Intrinsic" Heterogeneity of Somatic Variants in Microsatellite-Stable Colorectal Carcinomas and Their MetastasesMaja Hühns, Najim Ameziane, Carsten Holzmann, et al.
Plos One|January 4, 2013
Genotyping of fanconi anemia patients by whole exome sequencing: advantages and challengesKerstin Knies, Beatrice Schuster, Najim Ameziane, et al.
Archives of Neurology|October 11, 2002
Longitudinal brain volume measurement in multiple sclerosis: rate of brain atrophy is independent of the disease subtypeNynke F Kalkers, Najim Ameziane, Joost C J Bot, et al.
Frontiers in Genetics|February 24, 2023
Microbial contamination and composition of oral samples subjected to clinical whole genome sequencingAbhishek Kumar, Volha Skrahina, Joshua Atta, et al.
Anemia|July 11, 2012
Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger SequencingJohan J P Gille, Karijn Floor, Lianne Kerkhoven, et al.
Stem Cell Reviews and Reports|December 17, 2017
Bone Marrow Mesenchymal Stem Cells Carrying FANCD2 Mutation Differ from the Other Fanconi Anemia Complementation Groups in Terms of TGF-β1 ProductionIlgin Cagnan, Aysen Gunel-Ozcan, Fatima Aerts-Kaya, et al.
Human Mutation|January 24, 2006
Novel inactivating mutations of FANCC in Brazilian patients with Fanconi anemiaJane Yates, Winifred Keeble, Gerard Pals, et al.
Journal of Neurogenetics|November 20, 2020
<i>Biallelic ZNF335</i> mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophyAhmet Okay Caglayan, Kourosh Yaghouti, Tanyel Kockaya, et al.
American Journal of Medical Genetics. Part A|November 23, 2015
Novel FANCI mutations in Fanconi anemia with VACTERL associationSharon A Savage, Bari J Ballew, Neelam Giri, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
The Turkish Journal of Pediatrics|December 25, 2015
Molecular diagnosis of Fanconi anemia with next-generation sequencing in a case with subtle signs and a negative chromosomal breakage testDeniz Aslan, Najim Ameziane, Johan P De Winter
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 26, 2023
Clonal and "Intrinsic" Heterogeneity of Somatic Variants in Microsatellite-Stable Colorectal Carcinomas and Their MetastasesMaja Hühns, Najim Ameziane, Carsten Holzmann, et al.
Plos One|January 4, 2013
Genotyping of fanconi anemia patients by whole exome sequencing: advantages and challengesKerstin Knies, Beatrice Schuster, Najim Ameziane, et al.
Archives of Neurology|October 11, 2002
Longitudinal brain volume measurement in multiple sclerosis: rate of brain atrophy is independent of the disease subtypeNynke F Kalkers, Najim Ameziane, Joost C J Bot, et al.
Frontiers in Genetics|February 24, 2023
Microbial contamination and composition of oral samples subjected to clinical whole genome sequencingAbhishek Kumar, Volha Skrahina, Joshua Atta, et al.
Anemia|July 11, 2012
Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger SequencingJohan J P Gille, Karijn Floor, Lianne Kerkhoven, et al.
Stem Cell Reviews and Reports|December 17, 2017
Bone Marrow Mesenchymal Stem Cells Carrying FANCD2 Mutation Differ from the Other Fanconi Anemia Complementation Groups in Terms of TGF-β1 ProductionIlgin Cagnan, Aysen Gunel-Ozcan, Fatima Aerts-Kaya, et al.
Human Mutation|January 24, 2006
Novel inactivating mutations of FANCC in Brazilian patients with Fanconi anemiaJane Yates, Winifred Keeble, Gerard Pals, et al.
Journal of Neurogenetics|November 20, 2020
<i>Biallelic ZNF335</i> mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophyAhmet Okay Caglayan, Kourosh Yaghouti, Tanyel Kockaya, et al.
American Journal of Medical Genetics. Part A|November 23, 2015
Novel FANCI mutations in Fanconi anemia with VACTERL associationSharon A Savage, Bari J Ballew, Neelam Giri, et al.
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