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Academic Journal

The KRAS-variant is associated with risk of developing double primary breast and ovarian cancer.

  • Authors : Pilarski R; The Ohio State University Comprehensive Cancer Center and Department of Internal Medicine, Columbus, Ohio, United States of America. ; Patel DA

Subjects: Genes, ras* ; Genetic Variation* ; Mutation*

  • Source: PloS one [PLoS One] 2012; Vol. 7 (5), pp. e37891. Date of Electronic Publication: 2012 May 25.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic

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Academic Journal

Assessing BRCA1 activity in DNA damage repair using human induced pluripotent stem cells as an approach to assist classification of BRCA1 variants of uncertain significance.

  • Authors : Ozgencil M; Department of Medical & Molecular Genetics, King's College London, Faculty of Life Sciences & Medicine, London, United Kingdom.; Barwell J

Subjects: DNA Damage* ; DNA Repair* ; Genetic Predisposition to Disease*

  • Source: PloS one [PLoS One] 2021 Dec 02; Vol. 16 (12), pp. e0260852. Date of Electronic Publication: 2021 Dec 02 (Print Publication: 2021).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

The association between the expression of nuclear Yes-associated protein 1 (YAP1) and p53 protein expression profile in breast cancer patients.

  • Authors : Cha YJ; Department of Pathology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.; Kim D

Subjects: Mutation*; Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/*metabolism ; Transcription Factors/Transcription Factors/Transcription Factors/*metabolism

  • Source: PloS one [PLoS One] 2021 May 10; Vol. 16 (5), pp. e0250986. Date of Electronic Publication: 2021 May 10 (Print Publication: 2021).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation.

  • Authors : Susak H; Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.; Division of Computational Genomics and Systems Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Subjects: Genetic Variation*; Genome-Wide Association Study/Genome-Wide Association Study/Genome-Wide Association Study/*methods; Bayes Theorem

  • Source: PLoS computational biology [PLoS Comput Biol] 2021 Feb 19; Vol. 17 (2), pp. e1007784. Date of Electronic Publication: 2021 Feb 19 (Print Publication: 2021).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101238922 Publication Model: eCollection

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Academic Journal

Gene panel screening for insight towards breast cancer susceptibility in different ethnicities.

  • Authors : Bishop MR; Harrison School of Pharmacy, Department of Drug Discovery and Development, Auburn University, Auburn, Alabama, United States of America.; College of Veterinary Medicine, Department of Pathobiology, Auburn University, Auburn, Alabama, United States of America.

Subjects: Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics ; Genetic Variation/Genetic Variation/Genetic Variation/*genetics

  • Source: PloS one [PLoS One] 2020 Aug 31; Vol. 15 (8), pp. e0238295. Date of Electronic Publication: 2020 Aug 31 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

The genomic landscape of metastasis in treatment-naïve breast cancer models.

  • Authors : Ross C; Laboratory of Cancer Biology and Genetics, Metastasis Susceptibility Section, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States of America.; Szczepanek K

Subjects: Mutation*; Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*genetics ; Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*pathology

  • Source: PLoS genetics [PLoS Genet] 2020 May 28; Vol. 16 (5), pp. e1008743. Date of Electronic Publication: 2020 May 28 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection

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Academic Journal

Mitochondrial DNA mutations in Malaysian female breast cancer patients.

  • Authors : Omasanggar R; Department of Human Anatomy, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia.; Yu CY

Subjects: Mutation*; Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*genetics ; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics

  • Source: PloS one [PLoS One] 2020 May 22; Vol. 15 (5), pp. e0233461. Date of Electronic Publication: 2020 May 22 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

Association between mitochondrial genetic variation and breast cancer risk: The Multiethnic Cohort.

  • Authors : Li Y; Department of Epidemiology and Biostatistics, School of Medicine, University of California, San Francisco, California, United States of America.; Giorgi EE

Subjects: Genetic Predisposition to Disease* ; Genetic Variation*; Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*genetics

  • Source: PloS one [PLoS One] 2019 Oct 02; Vol. 14 (10), pp. e0222284. Date of Electronic Publication: 2019 Oct 02 (Print Publication: 2019).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

Discoveries beyond BRCA1/2: Multigene testing in an Asian multi-ethnic cohort suspected of hereditary breast cancer syndrome in the real world.

  • Authors : Ow SGW; Department of Hematology-Oncology, National University Cancer Institute, Singapore, Singapore.; Ong PY

Subjects: Mutation*; Asian People/Asian People/Asian People/*genetics ; BRCA1 Protein/BRCA1 Protein/BRCA1 Protein/*genetics

  • Source: PloS one [PLoS One] 2019 Mar 15; Vol. 14 (3), pp. e0213746. Date of Electronic Publication: 2019 Mar 15 (Print Publication: 2019).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

The combined survival effect of codon 72 polymorphisms and p53 somatic mutations in breast cancer depends on race and molecular subtype.

  • Authors : Hebert-Magee S; Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, United States of America.; Yu H

Subjects: Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*genetics ; Codon/Codon/Codon/*genetics ; Mutation/Mutation/Mutation/*genetics

  • Source: PloS one [PLoS One] 2019 Feb 07; Vol. 14 (2), pp. e0211734. Date of Electronic Publication: 2019 Feb 07 (Print Publication: 2019).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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