Ana Rebeca相关文献与解析，生知库 | 链接生命科学的每一步

Ribeiro, Aldaíza Marcos; Tavares, Lohanna Valeska de Sousa; Ciarlini, Nerci de Sá Cavalcante; Torres, Renan do Vale Farias; Sampaio, Virgínia Maria Ramos; Ponce, Ana Rebeca de Sousa; Peixoto, Paulo Henrique Soares; Magela, Mônica Fernandes; Bomfim, Marília de Andrade; Oliveira, Diane de Castro; Alves, Verônica Furtado; Fernandes, Maria Líllian Maia; Cavalcante, Karene Ferreira; Santos, Stephany Arruda; Freitas, Thais Magalhães de

发表日期：2025

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Mexican Patients With Suspected 22q11.2 Deletion Syndrome: Clinical Characterization and Molecular Findings by Fluorescence In Situ Hybridization and Multiplex Ligation-Dependent Probe Amplification

疑似22q11.2缺失综合征的墨西哥患者：临床特征及荧光原位杂交和多重连接依赖性探针扩增的分子检测结果

期刊:Molecular Genetics & Genomic Medicine

影响因子:1.6

doi:10.1002/mgg3.70153

Aguayo-Orozco, Thania Alejandra; Rivera, Horacio; Figuera, Luis E; Esparza-García, Eduardo; Perea-Díaz, Francisco Javier; Jaloma-Cruz, Ana Rebeca; Rizo-de la Torre, Lourdes Del Carmen; Domínguez-Quezada, Ma Guadalupe

发表日期：2025

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CRISPR/Cas9 Edition of the F9 Gene in Human Mesenchymal Stem Cells for Hemophilia B Therapy

利用 CRISPR/Cas9 技术对人骨髓间充质干细胞中的 F9 基因进行编辑，用于治疗 B 型血友病。

期刊:Life-Basel

影响因子:3.4

doi:10.3390/life14121640

Lara-Navarro, Irving Jair; Jave-Suárez, Luis Felipe; Marchal, Juan Antonio; Jaloma-Cruz, Ana Rebeca

Inverse Shifting-PCR Modified by Capillary Electrophoresis for Detecting F8 int22h and int1h Inversions in Severe Hemophilia A Patients and Probable Carriers

毛细管电泳改良的反向移位PCR法用于检测重度血友病A患者和可能携带者中的F8 int22h和int1h倒位

期刊:Life-Basel

影响因子:3.4

doi:10.3390/life14101332

Martínez-Contreras, Rosa Michel; García-López, Silvia Sofía; Luna-Záizar, Hilda; Jaloma-Cruz, Ana Rebeca

发表日期：2024

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In silico analysis of missense mutations in exons 1-5 of the F9 gene that cause hemophilia B

利用计算机模拟分析F9基因外显子1-5中导致B型血友病的错义突变。

期刊:BMC Bioinformatics

影响因子:3.3

doi:10.1186/s12859-019-2919-x

Meléndez-Aranda, Lennon; Jaloma-Cruz, Ana Rebeca; Pastor, Nina; Romero-Prado, Marina María de Jesús

发表日期：2019

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Genetic biomarkers related to hemarthrosis, inflammation, and cartilage structure in pediatric patients with hemophilic arthropathy

血友病性关节病患儿的关节积血、炎症和软骨结构相关的遗传生物标志物

期刊:Molecular Genetics & Genomic Medicine

影响因子:1.6

doi:10.1002/mgg3.979

López-Jiménez, José de Jesús; Ortega-Cervantes, Ricardo; Luna-Záizar, Hilda; Fletes-Rayas, Ana-Lilia; Beltrán-Miranda, Claudia-Patricia; Troyo-Sanromán, Rogelio; Soto-Padilla, Janet; Tlacuilo-Parra, Alberto; Jaloma-Cruz, Ana-Rebeca

An outbreak of salmonellosis in a pediatric hospital in Brazil

巴西一家儿科医院爆发沙门氏菌病疫情

Mexican Patients With Suspected 22q11.2 Deletion Syndrome: Clinical Characterization and Molecular Findings by Fluorescence In Situ Hybridization and Multiplex Ligation-Dependent Probe Amplification

疑似22q11.2缺失综合征的墨西哥患者：临床特征及荧光原位杂交和多重连接依赖性探针扩增的分子检测结果

CRISPR/Cas9 Edition of the F9 Gene in Human Mesenchymal Stem Cells for Hemophilia B Therapy

利用 CRISPR/Cas9 技术对人骨髓间充质干细胞中的 F9 基因进行编辑，用于治疗 B 型血友病。

Inverse Shifting-PCR Modified by Capillary Electrophoresis for Detecting F8 int22h and int1h Inversions in Severe Hemophilia A Patients and Probable Carriers

毛细管电泳改良的反向移位PCR法用于检测重度血友病A患者和可能携带者中的F8 int22h和int1h倒位

In silico analysis of missense mutations in exons 1-5 of the F9 gene that cause hemophilia B

利用计算机模拟分析F9基因外显子1-5中导致B型血友病的错义突变。

Genetic biomarkers related to hemarthrosis, inflammation, and cartilage structure in pediatric patients with hemophilic arthropathy

血友病性关节病患儿的关节积血、炎症和软骨结构相关的遗传生物标志物