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1
Deletion of MIF gene from live attenuated LdCen -/- parasites enhances protective CD4 + T cell immunity
Deletion of MIF gene from live attenuated LdCen -/- parasites enhances protective CD4 + T cell immunity
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Deletion of MIF gene from live attenuated LdCen -/- parasites enhances protective CD4 + T cell immunity

Fiuza, Jacqueline Araújo ; Gannavaram, Sreenivas ; Gaze, Soraya Torres ; de Ornellas, Letícia Gambogi ; Alves, Érica Alessandra ; Ismail, Nevien ; Nakhasi, Hira Lal ; Correa-Oliveira, Rodrigo

Scientific reports, 2023-05, Vol.13 (1), p.7362-7362, Article 7362 [Periódico revisado por pares]

England: Nature Publishing Group

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2
A 'suicide' CRISPR-Cas9 system to promote gene deletion and restoration by electroporation in Cryptococcus neoformans
A 'suicide' CRISPR-Cas9 system to promote gene deletion and restoration by electroporation in Cryptococcus neoformans
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A 'suicide' CRISPR-Cas9 system to promote gene deletion and restoration by electroporation in Cryptococcus neoformans

Wang, Yu ; Wei, Dongsheng ; Zhu, Xiangyang ; Pan, Jiao ; Zhang, Ping ; Huo, Liang ; Zhu, Xudong

Scientific reports, 2016-08, Vol.6 (1), p.31145, Article 31145 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Metabolic gene-deletion strains of Escherichia coli evolve to computationally predicted growth phenotypes
Metabolic gene-deletion strains of Escherichia coli evolve to computationally predicted growth phenotypes
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Metabolic gene-deletion strains of Escherichia coli evolve to computationally predicted growth phenotypes

Palsson, Bernhard Ø ; Fong, Stephen S

Nature genetics, 2004-10, Vol.36 (10), p.1056-1058 [Periódico revisado por pares]

London: Nature Publishing Group

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4
The Cdh5-CreERT2 transgene causes conditional Shb gene deletion in hematopoietic cells with consequences for immune cell responses to tumors
The Cdh5-CreERT2 transgene causes conditional Shb gene deletion in hematopoietic cells with consequences for immune cell responses to tumors
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The Cdh5-CreERT2 transgene causes conditional Shb gene deletion in hematopoietic cells with consequences for immune cell responses to tumors

He, Qi ; Li, Xiujuan ; Singh, Kailash ; Luo, Zhengkang ; Meija-Cordova, Mariela ; Jamalpour, Maria ; Lindahl, Björn ; Kriz, Vitezslav ; Vuolteenaho, Reetta ; Ulvmar, Maria ; Welsh, Michael

Scientific reports, 2019-05, Vol.9 (1), p.7548-8, Article 7548 [Periódico revisado por pares]

England: Nature Publishing Group

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5
Misdiagnosis of imported falciparum malaria from African areas due to an increased prevalence of pfhrp2/pfhrp3 gene deletion: the Djibouti case
Misdiagnosis of imported falciparum malaria from African areas due to an increased prevalence of pfhrp2/pfhrp3 gene deletion: the Djibouti case
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Misdiagnosis of imported falciparum malaria from African areas due to an increased prevalence of pfhrp2/pfhrp3 gene deletion: the Djibouti case

Iriart, Xavier ; Menard, Sandie ; Chauvin, Pamela ; Mohamed, Hasna S. ; Charpentier, Elena ; Mohamed, Mohamed A. ; Berry, Antoine ; Aboubaker, Mohamed H.

Emerging microbes & infections, 2020-01, Vol.9 (1), p.1984-1987 [Periódico revisado por pares]

United States: Taylor & Francis

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6
Bone marrow-specific Cap gene deletion protects against high-fat diet-induced insulin resistance
Bone marrow-specific Cap gene deletion protects against high-fat diet-induced insulin resistance
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Bone marrow-specific Cap gene deletion protects against high-fat diet-induced insulin resistance

Olefsky, Jerrold M ; Lesniewski, Lisa A ; Hosch, Sarah E ; Neels, Jaap G ; de Luca, Carl ; Pashmforoush, Mohammad ; Lumeng, Carey N ; Chiang, Shian-Huey ; Scadeng, Miriam ; Saltiel, Alan R

Nature medicine, 2007-04, Vol.13 (4), p.455-462 [Periódico revisado por pares]

United States: Nature Publishing Group

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7
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi―Goutiéres syndrome associated with mtDNA deletions
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi―Goutiéres syndrome associated with mtDNA deletions
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A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi―Goutiéres syndrome associated with mtDNA deletions

LESHINSKY-SILVER, Esther ; MALINGER, Gustavo ; LERMAN-SAGIE, Tally ; BEN-SIRA, Liat ; KIDRON, Dvora ; COHEN, Sarit ; INBAR, Shani ; BEZALELI, Tali ; LEVINE, Arie ; VINKLER, Chana ; LEV, Dorit

European journal of human genetics : EJHG, 2011-03, Vol.19 (3), p.287-292 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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8
Homozygous BCMA gene deletion in response to anti-BCMA CAR T cells in a patient with multiple myeloma
Homozygous BCMA gene deletion in response to anti-BCMA CAR T cells in a patient with multiple myeloma
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Homozygous BCMA gene deletion in response to anti-BCMA CAR T cells in a patient with multiple myeloma

Da Vià, Matteo C ; Dietrich, Oliver ; Truger, Marietta ; Arampatzi, Panagiota ; Duell, Johannes ; Heidemeier, Anke ; Zhou, Xiang ; Danhof, Sophia ; Kraus, Sabrina ; Chatterjee, Manik ; Meggendorfer, Manja ; Twardziok, Sven ; Goebeler, Maria-Elisabeth ; Topp, Max S ; Hudecek, Michael ; Prommersberger, Sabrina ; Hege, Kristen ; Kaiser, Shari ; Fuhr, Viktoria ; Weinhold, Niels ; Rosenwald, Andreas ; Erhard, Florian ; Haferlach, Claudia ; Einsele, Hermann ; Kortüm, K Martin ; Saliba, Antoine-Emmanuel ; Rasche, Leo

Nature medicine, 2021-04, Vol.27 (4), p.616-619 [Periódico revisado por pares]

United States: Nature Publishing Group

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9
Is it time to report carrier state for recessive disorders in every microarray analysis?-A pilot model based on hearing loss genes deletions
Is it time to report carrier state for recessive disorders in every microarray analysis?-A pilot model based on hearing loss genes deletions
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Is it time to report carrier state for recessive disorders in every microarray analysis?-A pilot model based on hearing loss genes deletions

Maya, Idit ; Basel-Salmon, Lina ; Sagi-Dain, Lena

European journal of human genetics : EJHG, 2021-08, Vol.29 (8), p.1292-1300 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage
Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage
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Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage

Obayashi, Masato ; Ishikawa, Kinya ; Izumi, Yuishin ; Takahashi, Makoto ; Niimi, Yusuke ; Sato, Nozomu ; Onodera, Osamu ; Kaji, Ryuji ; Nishizawa, Masatoyo ; Mizusawa, Hidehiro

Journal of human genetics, 2012-03, Vol.57 (3), p.202-206 [Periódico revisado por pares]

England: Nature Publishing Group

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