نتائج البحث

Elevated Mutation Burdens in Canadian Oat and Wheat Cultivars Released over the Past Century.

• Authors : Fu YB; Plant Gene Resources of Canada, Saskatoon Research and Development Centre, Agriculture and Agri-Food Canada, 107 Science Place, Saskatoon, SK S7N 0X2, Canada.; Horbach C

Subjects: Triticum*/Triticum*/Triticum*/genetics ; Avena*/Avena*/Avena*/genetics ; Mutation*/Mutation*/Mutation*/genetics

• Source: Cells [Cells] 2025 Jun 04; Vol. 14 (11). Date of Electronic Publication: 2025 Jun 04.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101600052 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4409

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Lessons from a National Liquid Biopsy Program to Provide Cancer Testing and Treatment for Patients with Advanced Solid Tumors †.

• Authors : Lapuk, Anna^1,2 (AUTHOR) ; Furman, Benjamin L. S.² (AUTHOR); Feijao, Pedro^1,2,3 (AUTHOR)

• Source: Current Oncology. Jan2026, Vol. 31 Issue 1, p18. 20p.

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Real-World Analysis of Post-Progression Treatment Patterns and Outcomes for EGFR Mutation-Positive Patients Treated with First-Line Osimertinib.

• Authors : Gibson, Amanda Jane Williams¹ (AUTHOR) ; Dean, Michelle Liane¹ (AUTHOR) ; Litt, Ishjot¹ (AUTHOR)

• Source: Current Oncology. May2024, Vol. 31 Issue 5, p2427-2440. 14p.

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The Clinical Utility of FLT3 Mutation Testing in Acute Leukemia: A Canadian Consensus.

• Authors : Bergeron J; CEMTL Installation Maisonneuve-Rosemont, Institut Universitaire d'Hématologie-Oncologie et de Thérapie Cellulaire, Université de Montréal, Montréal, QC H1T 2M4, Canada.; Capo-Chichi JM

Subjects: Leukemia, Myeloid, Acute*/Leukemia, Myeloid, Acute*/Leukemia, Myeloid, Acute*/genetics ; Hematopoietic Stem Cell Transplantation*; fms-Like Tyrosine Kinase 3/fms-Like Tyrosine Kinase 3/fms-Like Tyrosine Kinase 3/genetics

• Source: Current oncology (Toronto, Ont.) [Curr Oncol] 2023 Dec 12; Vol. 30 (12), pp. 10410-10436. Date of Electronic Publication: 2023 Dec 12.Publisher: MDPI Country of Publication: Switzerland NLM ID: 9502503 Publication Model: Electronic Cited Medium: Internet ISSN: 1718-7729

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Monkeypox genome mutation analysis using a timeseries model based on long short-term memory.

• Authors : Pathan, Refat Khan¹ (AUTHOR); Uddin, Mohammad Amaz² (AUTHOR) ; Paul, Ananda Mohan³ (AUTHOR)

• Source: PLoS ONE. 8/23/2023, Vol. 18 Issue 8, p1-17. 17p.

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Canadian Recommendations for Germline Genetic Testing of Patients with Breast Cancer: A Call to Action.

• Authors : Weber E; Division of Medical Genetics, Department of Specialized Medicine, McGill University Health Centre, Montréal, QC H4A 3J1, Canada.; Department of Human Genetics, McGill University, Montréal, QC H3A 1Y2, Canada.

Subjects: Breast Neoplasms*/Breast Neoplasms*/Breast Neoplasms*/genetics ; Breast Neoplasms*/Breast Neoplasms*/Breast Neoplasms*/diagnosis ; Genetic Testing*/Genetic Testing*/Genetic Testing*/methods

• Source: Current oncology (Toronto, Ont.) [Curr Oncol] 2025 May 22; Vol. 32 (6). Date of Electronic Publication: 2025 May 22.Publisher: MDPI Country of Publication: Switzerland NLM ID: 9502503 Publication Model: Electronic Cited Medium: Internet ISSN: 1718-7729

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Emergence of a mutation in the nucleocapsid gene of SARS-CoV-2 interferes with PCR detection in Canada.

• Authors : Isabel S; Department of Laboratory Medicine and Pathobiology, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.; Abdulnoor M

Subjects: COVID-19*/COVID-19*/COVID-19*/diagnosis ; COVID-19*/COVID-19*/COVID-19*/epidemiology ; SARS-CoV-2*/SARS-CoV-2*/SARS-CoV-2*/genetics

• Source: Scientific reports [Sci Rep] 2022 Jun 27; Vol. 12 (1), pp. 10867. Date of Electronic Publication: 2022 Jun 27.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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OTX2 mutation associated with severe myopia in a Canadian family.

• Authors : Wangding S; Department of Pediatrics, Schulich School of Medicine and Dentistry, London, Canada.; Colaiacovo S

Subjects: Myopia, Degenerative*/Myopia, Degenerative*/Myopia, Degenerative*/diagnosis ; Myopia, Degenerative*/Myopia, Degenerative*/Myopia, Degenerative*/genetics ; Retinal Dystrophies*/Retinal Dystrophies*/Retinal Dystrophies*/genetics

• Source: Ophthalmic genetics [Ophthalmic Genet] 2022 Jun; Vol. 43 (3), pp. 389-391. Date of Electronic Publication: 2021 Dec 26.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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From MAiD Referral to Targeted Therapy Success: A Case of BRAF -Mutated Anaplastic Thyroid Cancer.

• Authors : Stubbert, Brett¹ (AUTHOR); Stewart, Paul^1,2 (AUTHOR); Winquist, Eric^1,2,3 (AUTHOR)

• Source: Reports (MDPI AG). Mar2026, Vol. 9 Issue 1, p10. 8p.

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Molecular analysis of cystinosis: probable Irish origin of the most common French Canadian mutation.

• Authors : McGowan-Jordan J; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada.; Stoddard K

Subjects: Glycoproteins* ; Mutation*; Cystinosis/Cystinosis/Cystinosis/*genetics

• Source: European journal of human genetics : EJHG [Eur J Hum Genet] 1999 Sep; Vol. 7 (6), pp. 671-8.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print Cited Medium: Print ISSN: 1018-4813

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