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Antonio Rausell

Showing results (31-40 of 35) with videos related to

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The Journal of Allergy and Clinical Immunology|December 7, 2017
Generation of adult human T-cell progenitors for immunotherapeutic applicationsLaura Simons, Kuiying Ma, Corinne de Chappedelaine, et al.
Genome Medicine|March 25, 2026
COBT: a gene-based rare variant burden test for case-only study designs using aggregated genotypes from public reference cohortsAntoine Favier, Stefania Chounta, Alejandro Garcia, et al.
Cellular & Molecular Immunology|June 12, 2021
A DL-4- and TNFα-based culture system to generate high numbers of nonmodified or genetically modified immunotherapeutic human T-lymphoid progenitorsRanjita Devi Moirangthem, Kuiying Ma, Sabrina Lizot, et al.
American Journal of Human Genetics|April 7, 2022
Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with cerebellar hypoplasia and disrupt Purkinje cell differentiationMarion Coolen, Nami Altin, Karthyayani Rajamani, et al.
Cell Reports. Medicine|January 27, 2023
Severe hematopoietic stem cell inflammation compromises chronic granulomatous disease gene therapySteicy Sobrino, Alessandra Magnani, Michaela Semeraro, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
The Journal of Allergy and Clinical Immunology|December 7, 2017
Generation of adult human T-cell progenitors for immunotherapeutic applicationsLaura Simons, Kuiying Ma, Corinne de Chappedelaine, et al.
Genome Medicine|March 25, 2026
COBT: a gene-based rare variant burden test for case-only study designs using aggregated genotypes from public reference cohortsAntoine Favier, Stefania Chounta, Alejandro Garcia, et al.
Cellular & Molecular Immunology|June 12, 2021
A DL-4- and TNFα-based culture system to generate high numbers of nonmodified or genetically modified immunotherapeutic human T-lymphoid progenitorsRanjita Devi Moirangthem, Kuiying Ma, Sabrina Lizot, et al.
American Journal of Human Genetics|April 7, 2022
Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with cerebellar hypoplasia and disrupt Purkinje cell differentiationMarion Coolen, Nami Altin, Karthyayani Rajamani, et al.
Cell Reports. Medicine|January 27, 2023
Severe hematopoietic stem cell inflammation compromises chronic granulomatous disease gene therapySteicy Sobrino, Alessandra Magnani, Michaela Semeraro, et al.
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