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Fernando Rodrigues-Lima

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The Journal of Biological Chemistry|February 7, 2026
The SETD2 L1609P mutation found in leukemia disrupts methyltransferase activity and reduces histone H3K36 trimethylationChristina Michail, Jérémy Berthelet, Ariel E Mechaly, et al.
Nature Communications|February 3, 2023
Myelodysplastic Syndrome associated TET2 mutations affect NK cell function and genome methylationMaxime Boy, Valeria Bisio, Lin-Pierre Zhao, et al.
Blood|March 16, 2025
Blunted CD40-responsive enhancer activation in CREBBP-mutant lymphomas can be restored by enforced CD4 T-cell engagementHaopeng Yang, Wenchao Zhang, Vida Ravanmehr, et al.
Nature Communications|April 14, 2018
HSP27 is a partner of JAK2-STAT5 and a potential therapeutic target in myelofibrosisMargaux Sevin, Lucia Kubovcakova, Nicolas Pernet, et al.
The Journal of Experimental Medicine|July 19, 2024
Haploinsufficiency in PTPN2 leads to early-onset systemic autoimmunity from Evans syndrome to lupusMarie Jeanpierre, Jade Cognard, Maud Tusseau, et al.
Clinical Genetics|February 8, 2022
Systemic inflammatory syndrome in children with FARSA deficiencyFabienne Charbit-Henrion, Roman Goguyer-Deschaumes, Keren Borensztajn, et al.
Blood|March 15, 2017
<i>Crebbp</i> loss cooperates with <i>Bcl2</i> overexpression to promote lymphoma in miceIdoia García-Ramírez, Saber Tadros, Inés González-Herrero, et al.
Nature Communications|September 28, 2023
Author Correction: CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorderAurélie de Thonel, Johanna K Ahlskog, Kevin Daupin, et al.
Nature Communications|November 17, 2022
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorderAurélie de Thonel, Johanna K Ahlskog, Kevin Daupin, et al.
The Journal of Clinical Investigation|May 16, 2022
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical traffickingRémi Duclaux-Loras, Corinne Lebreton, Jérémy Berthelet, et al.
Pageof 12

Showing results (111-120 of 120) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 120 results.
The Journal of Biological Chemistry|February 7, 2026
The SETD2 L1609P mutation found in leukemia disrupts methyltransferase activity and reduces histone H3K36 trimethylationChristina Michail, Jérémy Berthelet, Ariel E Mechaly, et al.
Nature Communications|February 3, 2023
Myelodysplastic Syndrome associated TET2 mutations affect NK cell function and genome methylationMaxime Boy, Valeria Bisio, Lin-Pierre Zhao, et al.
Blood|March 16, 2025
Blunted CD40-responsive enhancer activation in CREBBP-mutant lymphomas can be restored by enforced CD4 T-cell engagementHaopeng Yang, Wenchao Zhang, Vida Ravanmehr, et al.
Nature Communications|April 14, 2018
HSP27 is a partner of JAK2-STAT5 and a potential therapeutic target in myelofibrosisMargaux Sevin, Lucia Kubovcakova, Nicolas Pernet, et al.
The Journal of Experimental Medicine|July 19, 2024
Haploinsufficiency in PTPN2 leads to early-onset systemic autoimmunity from Evans syndrome to lupusMarie Jeanpierre, Jade Cognard, Maud Tusseau, et al.
Clinical Genetics|February 8, 2022
Systemic inflammatory syndrome in children with FARSA deficiencyFabienne Charbit-Henrion, Roman Goguyer-Deschaumes, Keren Borensztajn, et al.
Blood|March 15, 2017
<i>Crebbp</i> loss cooperates with <i>Bcl2</i> overexpression to promote lymphoma in miceIdoia García-Ramírez, Saber Tadros, Inés González-Herrero, et al.
Nature Communications|September 28, 2023
Author Correction: CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorderAurélie de Thonel, Johanna K Ahlskog, Kevin Daupin, et al.
Nature Communications|November 17, 2022
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorderAurélie de Thonel, Johanna K Ahlskog, Kevin Daupin, et al.
The Journal of Clinical Investigation|May 16, 2022
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical traffickingRémi Duclaux-Loras, Corinne Lebreton, Jérémy Berthelet, et al.
Pageof 12