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J Majewski

Showing results (121-130 of 128) with videos related to

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The Journal of Pathology|May 11, 2013
Identification of recurrent FGFR3 fusion genes in lung cancer through kinome-centred RNA sequencingIan J Majewski, Lorenza Mittempergher, Nadia M Davidson, et al.
Clinical Genetics|February 8, 2017
Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole-exome sequencingT B Balci, T Hartley, Y Xi, et al.
Blood|January 15, 2020
Molecular patterns of response and treatment failure after frontline venetoclax combinations in older patients with AMLC D DiNardo, I S Tiong, A Quaglieri, et al.
Nature Communications|January 10, 2015
Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindnessS Kmoch, J Majewski, V Ramamurthy, et al.
Blood|April 7, 2021
Intact TP-53 function is essential for sustaining durable responses to BH3-mimetic drugs in leukemiasRachel Thijssen, Sarah T Diepstraten, Donia Moujalled, et al.
Clinical Genetics|August 19, 2015
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.
Nature Communications|June 21, 2020
A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunctionJoanne M Hildebrand, Maria Kauppi, Ian J Majewski, et al.
American Journal of Human Genetics|April 23, 2022
Germline MBD4 deficiency causes a multi-tumor predisposition syndromeClaire Palles, Hannah D West, Edward Chew, et al.
Pageof 13

Showing results (121-130 of 128) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 128 results.
The Journal of Pathology|May 11, 2013
Identification of recurrent FGFR3 fusion genes in lung cancer through kinome-centred RNA sequencingIan J Majewski, Lorenza Mittempergher, Nadia M Davidson, et al.
Clinical Genetics|February 8, 2017
Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole-exome sequencingT B Balci, T Hartley, Y Xi, et al.
Blood|January 15, 2020
Molecular patterns of response and treatment failure after frontline venetoclax combinations in older patients with AMLC D DiNardo, I S Tiong, A Quaglieri, et al.
Nature Communications|January 10, 2015
Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindnessS Kmoch, J Majewski, V Ramamurthy, et al.
Blood|April 7, 2021
Intact TP-53 function is essential for sustaining durable responses to BH3-mimetic drugs in leukemiasRachel Thijssen, Sarah T Diepstraten, Donia Moujalled, et al.
Clinical Genetics|August 19, 2015
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.
Nature Communications|June 21, 2020
A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunctionJoanne M Hildebrand, Maria Kauppi, Ian J Majewski, et al.
American Journal of Human Genetics|April 23, 2022
Germline MBD4 deficiency causes a multi-tumor predisposition syndromeClaire Palles, Hannah D West, Edward Chew, et al.
Pageof 13