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  • 1-10 of  699,369 نتائج ""Mutation""
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Academic Journal

Different mutations in SARS-CoV-2 associate with severe and mild outcome.

  • Authors : Nagy Á; Department of Bioinformatics, Semmelweis University, Budapest, Hungary; TTK Momentum Cancer Biomarker Research Group, Budapest, Hungary.

Subjects: Mutation*; COVID-19/COVID-19/COVID-19/*drug therapy ; COVID-19/COVID-19/COVID-19/*etiology

  • Source: International journal of antimicrobial agents [Int J Antimicrob Agents] 2021 Feb; Vol. 57 (2), pp. 106272. Date of Electronic Publication: 2020 Dec 23.Publisher: Elsevier Science Publishers Country of Publication: Netherlands NLM ID: 9111860 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Optimisation of an Electrochemical DNA Sensor for Measuring KRAS G12D and G13D Point Mutations in Different Tumour Types.

  • Authors : Attoye B; Department of Biomedical Engineering, University of Strathclyde, 40 George Street, Glasgow G1 1QE, UK.; Baker MJ

Subjects: Biosensing Techniques* ; Point Mutation*; DNA

  • Source: Biosensors [Biosensors (Basel)] 2021 Feb 05; Vol. 11 (2). Date of Electronic Publication: 2021 Feb 05.Publisher: MDPI Pub Country of Publication: Switzerland NLM ID: 101609191 Publication Model: Electronic Cited Medium: Internet ISSN: 2079-6374

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Academic Journal

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction.

Subjects: Mutation*; Matrix Attachment Region Binding Proteins/Matrix Attachment Region Binding Proteins/Matrix Attachment Region Binding Proteins/*genetics ; Neurodevelopmental Disorders/Neurodevelopmental Disorders/Neurodevelopmental Disorders/*genetics

  • Source: American journal of human genetics [Am J Hum Genet] 2021 Feb 04; Vol. 108 (2), pp. 346-356. Date of Electronic Publication: 2021 Jan 28.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

A Closer Look at Estrogen Receptor Mutations in Breast Cancer and Their Implications for Estrogen and Antiestrogen Responses.

  • Authors : Clusan L; Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement et Travail)-UMR_S1085, Rennes University, F-35000 Rennes, France.; Le Goff P

Subjects: Biomarkers, Tumor* ; Mutation*; Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*etiology

  • Source: International journal of molecular sciences [Int J Mol Sci] 2021 Jan 13; Vol. 22 (2). Date of Electronic Publication: 2021 Jan 13.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Academic Journal

Variant analysis of the first Lebanese SARS-CoV-2 isolates.

  • Authors : Abou-Hamdan M; Biology department, Faculty of sciences (I), Lebanese University, Beirut, LB, Lebanon.; Hamze K

Subjects: Genetic Variation* ; Genome, Viral* ; Mutation*

  • Source: Genomics [Genomics] 2021 Jan; Vol. 113 (1 Pt 2), pp. 892-895. Date of Electronic Publication: 2020 Oct 20.Publisher: Academic Press Country of Publication: United States NLM ID: 8800135 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Trends of mutation accumulation across global SARS-CoV-2 genomes: Implications for the evolution of the novel coronavirus.

  • Authors : Roy C; College of Veterinary Medicine, Western University of Health Sciences, 309 East Second Street, Pomona, CA 91766, USA.; Mandal SM

Subjects: Evolution, Molecular* ; Genome, Viral* ; Mutation Accumulation*

  • Source: Genomics [Genomics] 2020 Nov; Vol. 112 (6), pp. 5331-5342. Date of Electronic Publication: 2020 Nov 05.Publisher: Academic Press Country of Publication: United States NLM ID: 8800135 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Observation of nine previously reported and 10 non-reported SLC4A11 mutations among 20 Iranian CHED probands and identification of an MPDZ mutation as possible cause of CHED and FECD in one family.

  • Authors : Moazzeni H; School of Biology, College of Science,University of Tehran, Tehran, Iran.; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Subjects: Mutation*; Anion Transport Proteins/Anion Transport Proteins/Anion Transport Proteins/*genetics ; Antiporters/Antiporters/Antiporters/*genetics Corneal endothelial dystrophy type 2

  • Source: The British journal of ophthalmology [Br J Ophthalmol] 2020 Nov; Vol. 104 (11), pp. 1621-1628. Date of Electronic Publication: 2019 Aug 16.Publisher: BMJ Pub. Group Country of Publication: England NLM ID: 0421041 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Spontaneous Mutations in HIV-1 Gag, Protease, RT p66 in the First Replication Cycle and How They Appear: Insights from an In Vitro Assay on Mutation Rates and Types.

  • Authors : Yeo JY; Bioinformatics Institute, A*STAR, 30 Biopolis Street, #07-01 Matrix, Singapore 138671, Singapore.; Experimental Drug Development Centre, A*STAR, 10 Biopolis Road Chromos #05-01, Singapore 138670, Singapore.

Subjects: Mutation*; HIV Protease/HIV Protease/HIV Protease/*genetics ; HIV Reverse Transcriptase/HIV Reverse Transcriptase/HIV Reverse Transcriptase/*genetics

  • Source: International journal of molecular sciences [Int J Mol Sci] 2020 Dec 31; Vol. 22 (1). Date of Electronic Publication: 2020 Dec 31.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Academic Journal

A pan-cancer atlas of somatic mutations in miRNA biogenesis genes.

Subjects: Mutation*; DEAD-box RNA Helicases/DEAD-box RNA Helicases/DEAD-box RNA Helicases/*genetics ; MicroRNAs/MicroRNAs/MicroRNAs/*biosynthesis

  • Source: Nucleic acids research [Nucleic Acids Res] 2021 Jan 25; Vol. 49 (2), pp. 601-620.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes.

  • Authors : Byrjalsen A; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.; Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

Subjects: Germ-Line Mutation*; Genetic Testing/Genetic Testing/Genetic Testing/*statistics & numerical data ; Neoplastic Syndromes, Hereditary/Neoplastic Syndromes, Hereditary/Neoplastic Syndromes, Hereditary/*epidemiology

  • Source: PLoS genetics [PLoS Genet] 2020 Dec 17; Vol. 16 (12), pp. e1009231. Date of Electronic Publication: 2020 Dec 17 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet

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  • 1-10 of  699,369 نتائج ""Mutation""