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Estelle Chanudet

Showing results (11-20 of 27) with videos related to

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The Journal of Pathology|January 16, 2010
Splenic marginal zone lymphoma: characterization of 7q deletion and its value in diagnosisA James Watkins, Yuanxue Huang, Hongtao Ye, et al.
The Journal of Pathology|August 7, 2010
Primary effusion lymphoma: genomic profiling revealed amplification of SELPLG and CORO1C encoding for proteins important for cell migrationShi-Lu Luan, Emmanuelle Boulanger, Hongtao Ye, et al.
The Journal of Investigative Dermatology|February 9, 2013
Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRASVeronica A Kinsler, Anna C Thomas, Miho Ishida, et al.
The Journal of Investigative Dermatology|March 28, 2015
Acute Inhibition of MEK Suppresses Congenital Melanocytic Nevus Syndrome in a Murine Model Driven by Activated NRAS and Wnt SignalingJeffrey S Pawlikowski, Claire Brock, Sheau-Chiann Chen, et al.
Human Molecular Genetics|January 14, 2014
Mutation of SALL2 causes recessive ocular coloboma in humans and miceDaniel Kelberman, Lily Islam, Jörn Lakowski, et al.
Nature Genetics|November 19, 2013
Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndromeSérgio B Sousa, Dagan Jenkins, Estelle Chanudet, et al.
Virchows Archiv : an International Journal of Pathology|January 6, 2021
Morphological findings in frozen non-neoplastic kidney tissues of patients with kidney cancer from large-scale multicentric studies on renal cancerBehnoush Abedi-Ardekani, Dariush Nasrollahzadeh, Lars Egevad, et al.
Human Molecular Genetics|February 2, 2021
Sexual dimorphism in cancer: insights from transcriptional signatures in kidney tissue and renal cell carcinomaRuhina S Laskar, Peng Li, Szilvia Ecsedi, et al.
Ebiomedicine|July 6, 2016
Identification of Circulating Tumor DNA for the Early Detection of Small-cell Lung CancerLynnette Fernandez-Cuesta, Sandra Perdomo, Patrice H Avogbe, et al.
Plos One|December 20, 2012
Characterisation and validation of insertions and deletions in 173 patient exomesFrancesco Lescai, Silvia Bonfiglio, Chiara Bacchelli, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
The Journal of Pathology|January 16, 2010
Splenic marginal zone lymphoma: characterization of 7q deletion and its value in diagnosisA James Watkins, Yuanxue Huang, Hongtao Ye, et al.
The Journal of Pathology|August 7, 2010
Primary effusion lymphoma: genomic profiling revealed amplification of SELPLG and CORO1C encoding for proteins important for cell migrationShi-Lu Luan, Emmanuelle Boulanger, Hongtao Ye, et al.
The Journal of Investigative Dermatology|February 9, 2013
Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRASVeronica A Kinsler, Anna C Thomas, Miho Ishida, et al.
The Journal of Investigative Dermatology|March 28, 2015
Acute Inhibition of MEK Suppresses Congenital Melanocytic Nevus Syndrome in a Murine Model Driven by Activated NRAS and Wnt SignalingJeffrey S Pawlikowski, Claire Brock, Sheau-Chiann Chen, et al.
Human Molecular Genetics|January 14, 2014
Mutation of SALL2 causes recessive ocular coloboma in humans and miceDaniel Kelberman, Lily Islam, Jörn Lakowski, et al.
Nature Genetics|November 19, 2013
Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndromeSérgio B Sousa, Dagan Jenkins, Estelle Chanudet, et al.
Virchows Archiv : an International Journal of Pathology|January 6, 2021
Morphological findings in frozen non-neoplastic kidney tissues of patients with kidney cancer from large-scale multicentric studies on renal cancerBehnoush Abedi-Ardekani, Dariush Nasrollahzadeh, Lars Egevad, et al.
Human Molecular Genetics|February 2, 2021
Sexual dimorphism in cancer: insights from transcriptional signatures in kidney tissue and renal cell carcinomaRuhina S Laskar, Peng Li, Szilvia Ecsedi, et al.
Ebiomedicine|July 6, 2016
Identification of Circulating Tumor DNA for the Early Detection of Small-cell Lung CancerLynnette Fernandez-Cuesta, Sandra Perdomo, Patrice H Avogbe, et al.
Plos One|December 20, 2012
Characterisation and validation of insertions and deletions in 173 patient exomesFrancesco Lescai, Silvia Bonfiglio, Chiara Bacchelli, et al.
Pageof 3