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Djihad Hadjadj

Showing results (11-20 of 17) with videos related to

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Investigative Ophthalmology & Visual Science|August 20, 2025
Insights Into the FOXE3 Transcriptional Network and Disease Mechanisms From the Investigation of a Regulatory Variant Driving Complex MicrophthalmiaJulie Plaisancié, Clémentine Angée, Elisa Erjavec, et al.
American Journal of Human Genetics|September 18, 2024
Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopiaElisa Erjavec, Clémentine Angée, Djihad Hadjadj, et al.
Acta Neuropathologica|August 14, 2012
Frequent ATRX mutations and loss of expression in adult diffuse astrocytic tumors carrying IDH1/IDH2 and TP53 mutationsXiao-Yang Liu, Noha Gerges, Andrey Korshunov, et al.
Acta Neuropathologica|February 19, 2013
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomasAdam M Fontebasso, Jeremy Schwartzentruber, Dong-Anh Khuong-Quang, et al.
Nature Cancer|July 5, 2022
Structural variants shape driver combinations and outcomes in pediatric high-grade gliomaFrank P B Dubois, Ofer Shapira, Noah F Greenwald, et al.
Journal of Medical Genetics|August 4, 2025
Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with <i>NF1</i> point variantsLaurence Pacot, Marinus Blok, Dominique Vidaud, et al.
Cell|December 1, 2020
Histone H3.3G34-Mutant Interneuron Progenitors Co-opt PDGFRA for GliomagenesisCarol C L Chen, Shriya Deshmukh, Selin Jessa, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Investigative Ophthalmology & Visual Science|August 20, 2025
Insights Into the FOXE3 Transcriptional Network and Disease Mechanisms From the Investigation of a Regulatory Variant Driving Complex MicrophthalmiaJulie Plaisancié, Clémentine Angée, Elisa Erjavec, et al.
American Journal of Human Genetics|September 18, 2024
Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopiaElisa Erjavec, Clémentine Angée, Djihad Hadjadj, et al.
Acta Neuropathologica|August 14, 2012
Frequent ATRX mutations and loss of expression in adult diffuse astrocytic tumors carrying IDH1/IDH2 and TP53 mutationsXiao-Yang Liu, Noha Gerges, Andrey Korshunov, et al.
Acta Neuropathologica|February 19, 2013
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomasAdam M Fontebasso, Jeremy Schwartzentruber, Dong-Anh Khuong-Quang, et al.
Nature Cancer|July 5, 2022
Structural variants shape driver combinations and outcomes in pediatric high-grade gliomaFrank P B Dubois, Ofer Shapira, Noah F Greenwald, et al.
Journal of Medical Genetics|August 4, 2025
Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with <i>NF1</i> point variantsLaurence Pacot, Marinus Blok, Dominique Vidaud, et al.
Cell|December 1, 2020
Histone H3.3G34-Mutant Interneuron Progenitors Co-opt PDGFRA for GliomagenesisCarol C L Chen, Shriya Deshmukh, Selin Jessa, et al.
Pageof 2