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Djihad Hadjadj

Showing results (1-10 of 17) with videos related to

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Nature Medicine|October 20, 2020
Entering the era of precision medicine in pediatric oncologyDjihad Hadjadj, Shriya Deshmukh, Nada Jabado
Genomics Data|August 11, 2016
Characterization of the replication timing program of 6 human model cell linesDjihad Hadjadj, Thomas Denecker, Chrystelle Maric, et al.
NAR Genomics and Bioinformatics|February 12, 2021
Efficient, quick and easy-to-use DNA replication timing analysis with START-R suiteDjihad Hadjadj, Thomas Denecker, Eva Guérin, et al.
European Journal of Human Genetics : EJHG|February 2, 2023
Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1Laurence Pacot, Albain Chansavang, Sébastien Jacques, et al.
Aging|December 29, 2017
A hypothesis-driven approach identifies CDK4 and CDK6 inhibitors as candidate drugs for treatments of adrenocortical carcinomasDjihad Hadjadj, Su-Jung Kim, Thomas Denecker, et al.
International Journal of Molecular Sciences|January 21, 2023
Biology and Management of High-Grade Chondrosarcoma: An Update on Targets and Treatment OptionsCamille Tlemsani, Frédérique Larousserie, Sixtine De Percin, et al.
The British Journal of Dermatology|October 13, 2023
Identification of potential common genetic modifiers of neurofibromas: a genome-wide association study in 1333 patients with neurofibromatosis type 1Laurence Pacot, Audrey Sabbagh, Pierre Sohier, et al.
NPJ Genomic Medicine|September 8, 2024
Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaicsLaurence Pacot, Dominique Vidaud, Manuela Ye, et al.
European Journal of Endocrinology|December 17, 2025
PRKACA constitutional duplication: a specific cause of primary pigmented nodular adrenocortical diseasePatricia Vaduva, Florian Violon, Albain Chansavang, et al.
Human Genetics|August 8, 2022
Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1Laurence Pacot, Valerie Pelletier, Albain Chansavang, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Nature Medicine|October 20, 2020
Entering the era of precision medicine in pediatric oncologyDjihad Hadjadj, Shriya Deshmukh, Nada Jabado
Genomics Data|August 11, 2016
Characterization of the replication timing program of 6 human model cell linesDjihad Hadjadj, Thomas Denecker, Chrystelle Maric, et al.
NAR Genomics and Bioinformatics|February 12, 2021
Efficient, quick and easy-to-use DNA replication timing analysis with START-R suiteDjihad Hadjadj, Thomas Denecker, Eva Guérin, et al.
European Journal of Human Genetics : EJHG|February 2, 2023
Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1Laurence Pacot, Albain Chansavang, Sébastien Jacques, et al.
Aging|December 29, 2017
A hypothesis-driven approach identifies CDK4 and CDK6 inhibitors as candidate drugs for treatments of adrenocortical carcinomasDjihad Hadjadj, Su-Jung Kim, Thomas Denecker, et al.
International Journal of Molecular Sciences|January 21, 2023
Biology and Management of High-Grade Chondrosarcoma: An Update on Targets and Treatment OptionsCamille Tlemsani, Frédérique Larousserie, Sixtine De Percin, et al.
The British Journal of Dermatology|October 13, 2023
Identification of potential common genetic modifiers of neurofibromas: a genome-wide association study in 1333 patients with neurofibromatosis type 1Laurence Pacot, Audrey Sabbagh, Pierre Sohier, et al.
NPJ Genomic Medicine|September 8, 2024
Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaicsLaurence Pacot, Dominique Vidaud, Manuela Ye, et al.
European Journal of Endocrinology|December 17, 2025
PRKACA constitutional duplication: a specific cause of primary pigmented nodular adrenocortical diseasePatricia Vaduva, Florian Violon, Albain Chansavang, et al.
Human Genetics|August 8, 2022
Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1Laurence Pacot, Valerie Pelletier, Albain Chansavang, et al.
Pageof 2