Bệnh lý di truyền do đột biến gen
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Ngày đăng: 26/12/2023 19:16
Bệnh di truyền là nhóm bệnh lý có nguyên nhân do bất thường trong cấu trúc di truyền của một cá thể. Những bất thường về di truyền có thể dao động từ rất nhỏ cho đến rất lớn, từ một đột biến đơn gen của phân tử ADN bất thường nhiễm sắc thể (NST) về số lượng, cấu trúc hay toàn bộ NST ở người.
Bệnh di truyền có thể di truyền từ bố mẹ sang con cái hoặc do các đột biến mới phát sinh. Bệnh di truyền được chia thành 4 nhóm lớn dựa trên căn nguyên gây ra bệnh:
* Bệnh lý nhiễm sắc thể
* Bệnh di truyền đơn gen, đa gen
* Bệnh di truyền đa nhân tố
* Bệnh di truyền ty thể
Để hiểu rõ hơn Cục Thông tin khoa học và công nghệ quốc gia xin giới thiệu một số bài nghiên cứu đã được xuất bản chính thức và các bài viết được chấp nhận đăng trên những cơ sở dữ liệu học thuật chính thống.
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Midori Kimura, Sawako Matsuzaki, Kiyoko Kato
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Mehrdad Mozafar, Sina Kazemian, Mahsa Mayeli
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Christin Schmidtmann, Dierck Segelke, Georg Thaller
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17. Genetic diversity of Plasmodium vivax isolates from pregnant women in the Western Brazilian Amazon: A prospective cohort study
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Aquaculture and Fisheries 25 November 2021 Volume 8, Issue 2 (Cover date: March 2023) Pages 135-140
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Hao Yang, Xiao Tu, Zemao Gu
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32. Genetic screening of MMP1 as a potential pathogenic gene in chronic obstructive pulmonary disease
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Erkang Yi, Weitao Cao, Pixin Ran
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Soujanya Ganta, Prasanna Latha Komaravalli, Suman Latha Gaddam
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34. Genetic Diagnosis Impacts Medical Management for Pediatric Epilepsies
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Tingting Mo, Pinpin Long, Tangchun Wu
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Apinya Arnuphapprasert, Yudhi Ratna Nugraheni, Morakot Kaewthamasorn
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37. Non-invasive diagnosis of endometriosis: Immunologic and genetic markers
Clinica Chimica Acta 12 November 2022 Volume 538 (Cover date: 1 January 2023) Pages 70-86
Seyed Moein Mahini, Mohammad Younesi, Navid Jamali
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38. HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD). A statement from the HTAD working group of VASCERN
European Journal of Medical Genetics 29 November 2022 Volume 66, Issue 1 (Cover date: January 2023) Article 104673
Maryanne Caruana, Marieke J. Baars, Guillaume Jondeau
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39. Direct and maternal genetic effects for preinflection point growth traits and humoral immunity in quail
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Hojjat Sarvari-Kalouti, Ali Maghsoudi, Farzad Bagherzadeh-Kasmani
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Clara A. Moreau, Annabelle Harvey, Sebastien Jacquemont
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41. Genetic characteristics of suspected retinitis pigmentosa in a cohort of Chinese patients
Gene 2 December 2022 Volume 853 (Cover date: 15 February 2023) Article 147087
Bingyu Jin, Jing Li, Ming Yan
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42. High-quality read-based phasing of cystic fibrosis cohort informs genetic understanding of disease modification
Human Genetics and Genomics Advances 20 October 2022 Volume 4, Issue 1 (Cover date: 12 January 2023) Article 100156
Scott Mastromatteo, Angela Chen, Lisa J. Strug
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43. Comparative analysis unravels genetic recombination events of Vibrio parahaemolyticus recA gene
Infection, Genetics and Evolution 19 December 2022 Volume 107 (Cover date: January 2023) Article 105396
C. W. R. Gunasekara, L. G. T. G. Rajapaksha, S. H. M. P. Wimalasena
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44. Genetic diversity, population structure, linkage disequilibrium and GWAS for resistance to WSSV in Pacific white shrimp (Litopenaeus vannamei) using a 50K SNP chip
Aquaculture 16 September 2022 Volume 562 (Cover date: 15 January 2023) Article 738835
Thania Medrano-Mendoza, Baltasar F. García, Gabriel R. Campos-Montes
https://www.sciencedirect.com/science/article/pii/S0044848622009528/pdfft?md5=8636a3d12b000aafe94b1cabeecf8f78&pid=1-s2.0-S0044848622009528-main.pdf
45. Identification of Novel Gene Variants in Children With Drug-Resistant Epilepsy: Expanding the Genetic Spectrum
Pediatric Neurology 11 November 2022 Volume 139 (Cover date: February 2023) Pages 7-12
Ayca Kocaaga, Sevgi Yimenicioglu
https://www.sciencedirect.com/science/article/pii/S0887899422002375/pdfft?md5=c88c20e9d5a31cc4c682f17e76ba7274&pid=1-s2.0-S0887899422002375-main.pdf
46. Genetic risk score is associated with T2DM and diabetes complications risks
Gene 26 September 2022 Volume 849 (Cover date: 15 January 2023) Article 146921
Jaroslav A. Hubacek, Lucie Dlouha, Terezie Pelikanova
https://www.sciencedirect.com/science/article/pii/S0378111922007417/pdfft?md5=a370a080bef08bd7d538f0c7c9bb7936&pid=1-s2.0-S0378111922007417-main.pdf
47. Identification of RP1 as the genetic cause of retinitis pigmentosa in a multi-generational pedigree using Extremely Low-Coverage Whole Genome Sequencing (XLC-WGS)
Gene 27 October 2022 Volume 851 (Cover date: 30 January 2023) Article 146956
José M. Lázaro-Guevara, Bryan-Josué Flores-Robles, Stéphanie C. Thébault
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48. ECG-based techniques to enhance clinical practice in cardiac genetic disease management
Journal of Electrocardiology 14 November 2022 Volume 76 (Cover date: January–February 2023) Pages 55-60
Machteld Boonstra, Manon Kloosterman, Peter Loh
https://www.sciencedirect.com/science/article/pii/S002207362200214X/pdfft?md5=5ff80e3b55c9961db56041d7db27515b&pid=1-s2.0-S002207362200214X-main.pdf
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