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Results for
""Sequence Deletion""[mesh_terms]

232 Results

Searching titles within these results

Characterization of the Positive Transcription Regulator PfaR for Improving Eicosapentaenoic Acid Production in Shewanella putrefaciens W3-18-1.

Hehong Wei, Penghui He, Dianzhen Yu, Shuangyuan Liu, Chengtao Li, Dongru Qiu

Applied and environmental microbiology 2023;89(4):e0002123

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De novo familial adenomatous polyposis associated thyroid cancer with a c.2929delG frameshift deletion mutation in APC: a case report and literature review.

Miaorong Xu, Yuyan Zheng, Zhongchao Zuo, Qin Zhou, Qun Deng, Jianwei Wang, Da Wang

World journal of surgical oncology 2023;21(1):73

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Characterization of a Sabin-like type 2/3 recombinant poliovirus with a triple nucleotide deletion in the VP1 region isolated from sewage.

Jie Lin, Lei Zhou, Chenglin Zhu, Jichen Li, Wei Zhang, Shuangli Zhu, Dongyan Wang, Xiaolei Li, Hui Zhu, Qian Yang, Tianjiao Ji, Jinbo Xiao, Lan Yang, Kaitao Xiao, Kexin Shao, Yong Zhang, Dongmei Yan

Virology journal 2025;22(1):387

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α-Globin gene mutations in Isfahan Province, Iran.

Arezo Karamzade, Hadi Mirzapour, Majid Hoseinzade, Sara Asadi, Tahere Gholamrezapour, Parvaneh Tavakoli, Mansoor Salehi

Hemoglobin 2015;38(3):161-4

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Transcription could be the key to the selection advantage of mitochondrial deletion mutants in aging.

Axel Kowald, Thomas B L Kirkwood

Proceedings of the National Academy of Sciences of the United States of America 2014;111(8):2972-7

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Analyzing Change in Protein Stability Associated with Single Point Deletions in a Newly Defined Protein Structure Database.

Anupam Banerjee, Yaakov Levy, Pralay Mitra

Journal of proteome research 2020;18(3):1402-1410

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Cerebrospinal fluid monoamines, pterins, and folate in patients with mitochondrial diseases: systematic review and hospital experience.

Marta Batllori, Marta Molero-Luis, Aida Ormazabal, Raquel Montero, Cristina Sierra, Antonia Ribes, Julio Montoya, Eduardo Ruiz-Pesini, Mar O'Callaghan, Leticia Pias, Andrés Nascimento, Francesc Palau, Judith Armstrong, Delia Yubero, Juan D Ortigoza-Escobar, Angels García-Cazorla, Rafael Artuch

Journal of inherited metabolic disease 2019;41(6):1147-1158

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A Novel VPS13A Deletion in VPS13A Disease (Chorea-Acanthocytosis): A Case Report with Brief Literature Summary.

Benedetta Perrone, Viviana Mosca, Martina Pecoraro, Paola Ruffo, Elda Del Giudice, Alberta Leon, Martina Maino, Vincenzo La Bella, Rossella Spataro, Francesca Luisa Conforti

International journal of molecular sciences 2025;26(23):

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A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx.

Maria Isabel Bahamonde, Selma Angèlica Serra, Oliver Drechsel, Rubayte Rahman, Anna Marcé-Grau, Marta Prieto, Stephan Ossowski, Alfons Macaya, José M Fernández-Fernández

PloS one 2016;10(12):e0146035

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Role of the Escherichia coli glgX gene in glycogen metabolism.

David Dauvillée, Isabelle S Kinderf, Zhongyi Li, Behjat Kosar-Hashemi, Michael S Samuel, Lynette Rampling, Steven Ball, Matthew K Morell

Journal of bacteriology 2005;187(4):1465-73

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Hb H disease: clinical course and disease modifiers.

Vip Viprakasit, Suthat Fucharoen

Hematology. American Society of Hematology. Education Program 2010

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Mitochondrial DNA disease-molecular insights and potential routes to a cure.

Oliver Russell, Doug Turnbull

Experimental cell research 2014;325(1):38-43

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Site-directed mutagenesis mediated by a single polymerase chain reaction product.

Xueni Chen, Weimin Liu, Ileana Quinto, Giuseppe Scala

Methods in molecular biology (Clifton, N.J.) 2002;182():67-70

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Production of trans-2,3-dihydro-3-hydroxyanthranilic acid by engineered Pseudomonas chlororaphis GP72.

Hongbo Hu, Yifan Li, Kaiquan Liu, Jia Zhao, Wei Wang, Xuehong Zhang

Applied microbiology and biotechnology 2018;101(17):6607-6613

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Functional analysis of the split Synechocystis DnaE intein in plant tissues by biolistic particle bombardment.

Tina V Henry-Smith, Jianjun Yang, Min Qi

Transgenic research 2006;15(5):583-93

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Results: 1 – 15 / 232

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Results for ""Sequence Deletion""[mesh_terms]

Characterization of the Positive Transcription Regulator PfaR for Improving Eicosapentaenoic Acid Production in Shewanella putrefaciens W3-18-1.

De novo familial adenomatous polyposis associated thyroid cancer with a c.2929delG frameshift deletion mutation in APC: a case report and literature review.

Characterization of a Sabin-like type 2/3 recombinant poliovirus with a triple nucleotide deletion in the VP1 region isolated from sewage.

α-Globin gene mutations in Isfahan Province, Iran.

Transcription could be the key to the selection advantage of mitochondrial deletion mutants in aging.

Analyzing Change in Protein Stability Associated with Single Point Deletions in a Newly Defined Protein Structure Database.

Cerebrospinal fluid monoamines, pterins, and folate in patients with mitochondrial diseases: systematic review and hospital experience.

A Novel VPS13A Deletion in VPS13A Disease (Chorea-Acanthocytosis): A Case Report with Brief Literature Summary.

A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx.

Role of the Escherichia coli glgX gene in glycogen metabolism.

Hb H disease: clinical course and disease modifiers.

Mitochondrial DNA disease-molecular insights and potential routes to a cure.

Site-directed mutagenesis mediated by a single polymerase chain reaction product.

Production of trans-2,3-dihydro-3-hydroxyanthranilic acid by engineered Pseudomonas chlororaphis GP72.

Functional analysis of the split Synechocystis DnaE intein in plant tissues by biolistic particle bombardment.

Results for
""Sequence Deletion""[mesh_terms]