Search Results

Display Settings
Results per page: 10
Sort By: Relevance
Filter
  • 1-10 of  5,136,612 results for ""Mutation""

Your Filters

Reset filters
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

Is the Homologous Recombination Repair Mutation Defined by a 15-Gene Panel Associated with the Prognosis of Epithelial Ovarian Cancer?

  • Authors : Liu Y; Department of Obstetrics and Gynecology, Core Facility Center, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230001, Anhui, China.; Chen X

Subjects: Carcinoma, Ovarian Epithelial*/Carcinoma, Ovarian Epithelial*/Carcinoma, Ovarian Epithelial*/genetics ; Carcinoma, Ovarian Epithelial*/Carcinoma, Ovarian Epithelial*/Carcinoma, Ovarian Epithelial*/mortality ; Carcinoma, Ovarian Epithelial*/Carcinoma, Ovarian Epithelial*/Carcinoma, Ovarian Epithelial*/pathology

  • Source: Molecular diagnosis & therapy [Mol Diagn Ther] 2024 Sep; Vol. 28 (5), pp. 621-632. Date of Electronic Publication: 2024 Jul 05.Publisher: Adis, Springer International Country of Publication: New Zealand NLM ID: 101264260 Publication Model: Print-Electronic Cited Medium: Internet

Record details

Read More Add to Saved list
×
Academic Journal

Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis.

Subjects: Telangiectasia, Hereditary Hemorrhagic*/Telangiectasia, Hereditary Hemorrhagic*/Telangiectasia, Hereditary Hemorrhagic*/genetics ; Telangiectasia, Hereditary Hemorrhagic*/Telangiectasia, Hereditary Hemorrhagic*/Telangiectasia, Hereditary Hemorrhagic*/pathology ; Arteriovenous Malformations*/Arteriovenous Malformations*/Arteriovenous Malformations*/genetics

  • Source: American journal of human genetics [Am J Hum Genet] 2024 Oct 03; Vol. 111 (10), pp. 2283-2298. Date of Electronic Publication: 2024 Sep 18.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

Differential methylation of circulating free DNA assessed through cfMeDiP as a new tool for breast cancer diagnosis and detection of BRCA1/2 mutation.

  • Authors : Grisolia P; Sylvester Comprehensive Cancer Center and Department of Public Health Sciences, Miller School of Medicine, University of Miami, Miami, FL, USA.; Laboratory of Molecular and Precision Oncology, Biogem, IRGS, Ariano Irpino, Italy.

Subjects: Breast Neoplasms*/Breast Neoplasms*/Breast Neoplasms*/genetics ; Breast Neoplasms*/Breast Neoplasms*/Breast Neoplasms*/blood ; Breast Neoplasms*/Breast Neoplasms*/Breast Neoplasms*/diagnosis

  • Source: Journal of translational medicine [J Transl Med] 2024 Oct 15; Vol. 22 (1), pp. 938. Date of Electronic Publication: 2024 Oct 15.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876

Record details

Read More Add to Saved list
×
Academic Journal

Clinical utility of BRCA and ATM mutation status in circulating tumour DNA for treatment selection in advanced pancreatic cancer.

  • Authors : Sudo K; Department of Gastroenterology, Chiba Cancer Center, Chiba, Japan.; Nakamura Y

Subjects: Ataxia Telangiectasia Mutated Proteins*/Ataxia Telangiectasia Mutated Proteins*/Ataxia Telangiectasia Mutated Proteins*/genetics ; Pancreatic Neoplasms*/Pancreatic Neoplasms*/Pancreatic Neoplasms*/genetics ; Pancreatic Neoplasms*/Pancreatic Neoplasms*/Pancreatic Neoplasms*/drug therapy

  • Source: British journal of cancer [Br J Cancer] 2024 Oct; Vol. 131 (7), pp. 1237-1245. Date of Electronic Publication: 2024 Aug 28.Publisher: Nature Publishing Group on behalf of Cancer Research UK Country of Publication: England NLM ID: 0370635 Publication Model: Print-Electronic Cited

Record details

Read More Add to Saved list
×
Academic Journal

[Characterization of 19 novel gene mutation sites associated with autosome-dominant polycystic kidney disease].

  • Authors : Yang JL; Southeast University School of Medicine, Nanjing 210009, China Department of Nephrology, Zhong Da Hospital Southeast University, Nanjing 210009, China.; Peng SQ

Subjects: Polycystic Kidney, Autosomal Dominant*/Polycystic Kidney, Autosomal Dominant*/Polycystic Kidney, Autosomal Dominant*/genetics ; Mutation*; Humans

  • Source: Zhonghua nei ke za zhi [Zhonghua Nei Ke Za Zhi] 2024 Sep 01; Vol. 63 (9), pp. 866-873.Publisher: Zhonghua yi xue hui Country of Publication: China NLM ID: 16210490R Publication Model: Print Cited Medium: Print ISSN: 0578-1426

Record details

Read More Add to Saved list
×
Academic Journal

Only FLT3-ITD co-mutation did not have a deleterious effect on acute myeloid leukemia patients with NPM1 mutation, but concomitant with DNMT3A co-mutation or a < 3log reduction of MRD2 predicted poor survival.

  • Authors : Duan W; Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematology Disease, Beijing, China.; Jia J

Subjects: Nucleophosmin* ; DNA Methyltransferase 3A* ; fms-Like Tyrosine Kinase 3*/fms-Like Tyrosine Kinase 3*/fms-Like Tyrosine Kinase 3*/genetics

  • Source: Annals of hematology [Ann Hematol] 2024 Nov; Vol. 103 (11), pp. 4525-4535. Date of Electronic Publication: 2024 Sep 17.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 9107334 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

[Neurodevelopmental impact of a mutation in the RHOBTB2 gene].

Subjects: Mutation*; Humans ; Animals

  • Source: Revue medicale de Liege [Rev Med Liege] 2024 Jul; Vol. 79 (7-8), pp. 467-470.Publisher: Hopital De Baviere Country of Publication: Belgium NLM ID: 0404317 Publication Model: Print Cited Medium: Print ISSN: 0370-629X

Record details

Read More Add to Saved list
×
Academic Journal

KRAS G12C mutation in NSCLC in a small genetic center: insights into sotorasib therapy response potential.

  • Authors : Eser M; Department of Medical Genetics, Umraniye Education and Research Hospital, University of Health Sciences, Istanbul, Turkey.; Hekimoglu G

Subjects: Carcinoma, Non-Small-Cell Lung*/Carcinoma, Non-Small-Cell Lung*/Carcinoma, Non-Small-Cell Lung*/genetics ; Carcinoma, Non-Small-Cell Lung*/Carcinoma, Non-Small-Cell Lung*/Carcinoma, Non-Small-Cell Lung*/drug therapy ; Carcinoma, Non-Small-Cell Lung*/Carcinoma, Non-Small-Cell Lung*/Carcinoma, Non-Small-Cell Lung*/pathology

  • Source: Scientific reports [Sci Rep] 2024 Nov 04; Vol. 14 (1), pp. 26581. Date of Electronic Publication: 2024 Nov 04.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

Novel insights into presenilin 1 mutation associated with a distinctive dementia phenotype and cotton wool plaques.

  • Authors : Yamagata HD; Department of Clinical Laboratory Science, Tenri University, Nara, Japan. .; Akatsu H

Subjects: Presenilin-1*/Presenilin-1*/Presenilin-1*/genetics ; Plaque, Amyloid*/Plaque, Amyloid*/Plaque, Amyloid*/genetics ; Plaque, Amyloid*/Plaque, Amyloid*/Plaque, Amyloid*/pathology

  • Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2024 Oct; Vol. 45 (10), pp. 4829-4835. Publisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
Academic Journal

Understanding Osaka mutation polymorphic Aβ fibril response to static and oscillating electric fields: insights from computational modeling.

  • Authors : Makhkamov M; Laboratory of Experimental Biophysics, Centre for Advanced Technologies, Universitet 7, 100174, Tashkent, Uzbekistan.; Department of Information Technologies, Tashkent International University of Education, Imom Bukhoriy 6, 100207, Tashkent, Uzbekistan.

Subjects: Amyloid beta-Peptides*/Amyloid beta-Peptides*/Amyloid beta-Peptides*/metabolism ; Amyloid beta-Peptides*/Amyloid beta-Peptides*/Amyloid beta-Peptides*/genetics ; Amyloid beta-Peptides*/Amyloid beta-Peptides*/Amyloid beta-Peptides*/chemistry

  • Source: Scientific reports [Sci Rep] 2024 Sep 27; Vol. 14 (1), pp. 22246. Date of Electronic Publication: 2024 Sep 27.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

Record details

Read More Add to Saved list
×
  • 1-10 of  5,136,612 results for ""Mutation""