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Ana Borges

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

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Proceedings of the National Academy of Sciences of the United States of America|December 8, 2025
Combination of Cas9 and adeno-associated vectors enables efficient in vivo knockdown of precise miRNAs in the rodent and primate brainDavid Roura-Martinez, Natalia Popa, Florence Jaouen, et al.
Human Mutation|December 28, 2006
Truncation of NHEJ1 in a patient with polymicrogyriaVincent Cantagrel, Anne-Marie Lossi, Steven Lisgo, et al.
Theriogenology|April 20, 2025
Effect of injection conditions on the efficiency of intrafollicular immature oocyte transfer (IFIOT)Ana Caroline Chaves Vall Nicolás, Otávio Augusto Costa de Faria, Marcelo Sant Ana Borges, et al.
Epilepsia|July 21, 2011
Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutationsMathieu Milh, Nathalie Villeneuve, Mondher Chouchane, et al.
American Journal of Human Genetics|September 10, 2013
Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatusPierre Cacciagli, Julie Sutera-Sardo, Ana Borges-Correia, et al.
Pageof 4

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.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2025
Combination of Cas9 and adeno-associated vectors enables efficient in vivo knockdown of precise miRNAs in the rodent and primate brainDavid Roura-Martinez, Natalia Popa, Florence Jaouen, et al.
Human Mutation|December 28, 2006
Truncation of NHEJ1 in a patient with polymicrogyriaVincent Cantagrel, Anne-Marie Lossi, Steven Lisgo, et al.
Theriogenology|April 20, 2025
Effect of injection conditions on the efficiency of intrafollicular immature oocyte transfer (IFIOT)Ana Caroline Chaves Vall Nicolás, Otávio Augusto Costa de Faria, Marcelo Sant Ana Borges, et al.
Epilepsia|July 21, 2011
Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutationsMathieu Milh, Nathalie Villeneuve, Mondher Chouchane, et al.
American Journal of Human Genetics|September 10, 2013
Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatusPierre Cacciagli, Julie Sutera-Sardo, Ana Borges-Correia, et al.
Pageof 4