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Lucia Cavelier

Showing results (11-20 of 56) with videos related to

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Nature Communications|July 12, 2022
Ultra-sensitive monitoring of leukemia patients using superRCA mutation detection assaysLei Chen, Anna Eriksson, Simone Weström, et al.
BMC Biotechnology|November 15, 2013
Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissuesAmmar Zaghlool, Adam Ameur, Linnea Nyberg, et al.
Lakartidningen|May 11, 2021
[Precision diagnostics and therapy in hematological malignancies]Eva Hellström Lindberg, Lucia Cavelier, Jörg Cammenga, et al.
Nature Structural & Molecular Biology|November 8, 2011
Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brainAdam Ameur, Ammar Zaghlool, Jonatan Halvardson, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|October 7, 2017
Tumor SHB gene expression affects disease characteristics in human acute myeloid leukemiaMaria Jamalpour, Xiujuan Li, Lucia Cavelier, et al.
Molecular Aspects of Medicine|February 8, 2024
Current and emerging sequencing-based tools for precision cancer medicineAnders Edsjö, David Gisselsson, Johan Staaf, et al.
BMC Cancer|April 17, 2015
Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencingLucia Cavelier, Adam Ameur, Susana Häggqvist, et al.
Hemasphere|August 8, 2022
Five Percent Variant Allele Frequency Is a Reliable Reporting Threshold for <i>TP53</i> Variants Detected by Next Generation Sequencing in Chronic Lymphocytic Leukemia in the Clinical SettingTatjana Pandzic, Claes Ladenvall, Marie Engvall, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 6, 2023
Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid LeukemiaAnna Eriksson, Marie Engvall, Lucy Mathot, et al.
BMC Research Notes|November 23, 2012
Sequence based analysis of U-2973, a cell line established from a double-hit B-cell lymphoma with concurrent MYC and BCL2 rearrangementsSean D Hooper, Xiang Jiao, Elisabeth Sundström, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Nature Communications|July 12, 2022
Ultra-sensitive monitoring of leukemia patients using superRCA mutation detection assaysLei Chen, Anna Eriksson, Simone Weström, et al.
BMC Biotechnology|November 15, 2013
Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissuesAmmar Zaghlool, Adam Ameur, Linnea Nyberg, et al.
Lakartidningen|May 11, 2021
[Precision diagnostics and therapy in hematological malignancies]Eva Hellström Lindberg, Lucia Cavelier, Jörg Cammenga, et al.
Nature Structural & Molecular Biology|November 8, 2011
Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brainAdam Ameur, Ammar Zaghlool, Jonatan Halvardson, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|October 7, 2017
Tumor SHB gene expression affects disease characteristics in human acute myeloid leukemiaMaria Jamalpour, Xiujuan Li, Lucia Cavelier, et al.
Molecular Aspects of Medicine|February 8, 2024
Current and emerging sequencing-based tools for precision cancer medicineAnders Edsjö, David Gisselsson, Johan Staaf, et al.
BMC Cancer|April 17, 2015
Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencingLucia Cavelier, Adam Ameur, Susana Häggqvist, et al.
Hemasphere|August 8, 2022
Five Percent Variant Allele Frequency Is a Reliable Reporting Threshold for <i>TP53</i> Variants Detected by Next Generation Sequencing in Chronic Lymphocytic Leukemia in the Clinical SettingTatjana Pandzic, Claes Ladenvall, Marie Engvall, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 6, 2023
Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid LeukemiaAnna Eriksson, Marie Engvall, Lucy Mathot, et al.
BMC Research Notes|November 23, 2012
Sequence based analysis of U-2973, a cell line established from a double-hit B-cell lymphoma with concurrent MYC and BCL2 rearrangementsSean D Hooper, Xiang Jiao, Elisabeth Sundström, et al.
Pageof 6