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4.7 - RF-to-dc Energy Conversion in Beam-Type Devices

Generation, Transmission, Rectification, 1968, p.320-338

1968

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566 IDENTIFICATION OF GENETIC MARKERS ASSOCIATED WITH RESPONSE TO BACILLUS CALMETTE-GUÉRIN INTRAVESICAL THERAPY IN NON-MUSCLE-INVASIVE BLADDER CANCER

The Journal of urology, 2012-04, Vol.187 (4), p.e231-e231

2012

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915 EXOME SEQUENCING OF EXTREME PHENOTYPES TO IDENTIFY VARIANTS PREDICTIVE OF RESPONSE TO CHEMOTHERAPY IN BLADDER CANCER

The Journal of urology, 2013-04, Vol.189 (4), p.e376-e376

2013

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995 ANALYSIS OF STATIN MEDICATION, GENETIC VARIATION AND PROSTATE CANCER OUTCOMES

The Journal of urology, 2011-04, Vol.185 (4), p.e401-e401

2011

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995 ANALYSIS OF STATIN MEDICATION, GENETIC VARIATION AND PROSTATE CANCER OUTCOMES

The Journal of urology, 2011, Vol.185 (4), p.e401-e401

2011

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Abstract 1281: Germline mutations in NBN conferring DNA damage response defects are found in patients with multiple cancer types

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.1281-1281

2017

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Abstract 1291: High and moderate penetrance germline mutations in a number of genes are responsible for a small proportion of familial breast cancer risk in BRCAx families

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.1291-1291

2014

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Abstract 1318: A genome-wide association study of Waldenström macroglobulinemia/lymphoplasmacytic lymphoma demonstrates association with chromosome 6

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.1318-1318

2017

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Abstract 1572: Inherited truncating RAD52 variant discovered using integrated germline- somatic analysis predicts clinical outcome in patients with lung cancers

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.1572-1572

2019

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Abstract 2033: Germline mutations in ETV6 confer risk of thrombocytopenia and acute lymphocytic leukemia

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.2033-2033

2015

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Abstract 221: Inherited variants at 3q13.33 and 3p24.1 influences risk of diffuse large B-cell lymphoma

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.221-221

2018

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Abstract 2378: Harmonization of next generation sequencing data within consortia for gene discovery in familial breast cancer

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.2378-2378

2014

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Abstract 2600: SLX4 mutation in hereditary breast cancer

Cancer research (Chicago, Ill.), 2012-04, Vol.72 (8_Supplement), p.2600-2600

2012

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Abstract 2742: Potential burden of germline findings in targeted tumor sequencing using matched normal DNA

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.2742-2742

2015

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Abstract 3258: Preclinical evaluation of enhanced irofulven antitumor activity in an ERCC3 mutant background by in vitro and in vivo tumor models

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.3258-3258

2018

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Abstract 3282: Determination of cancer susceptibility in probands with breast and ovarian cancer

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.3282-3282

2014

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Abstract 4265: Risks of familial breast cancer associated with known and proposed breast cancer susceptibility genes

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.4265-4265

2017

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Abstract 4280: FH (rs367543046, chr1:241661227 A/ATTT) heterozygous carrier status does not confer risk to hereditary leiomyomatosis and renal cell cancer (HLRCC) and prostate cancer

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.4280-4280

2017

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Abstract 4626: Genetic susceptibility to diffuse large B-cell lymphoma in a pooled study of three Eastern Asian populations

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.4626-4626

2015

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Abstract 5071: A genome-wide association study suggests evidence of variants at 6p21.32 associated with marginal zone lymphoma

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.5071-5071

2014

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Abstract 5220: Evaluation of ACMG guideline classified variants in 180 cancer and incidental non-cancer genes in families with breast/ovarian cancer

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (14_Supplement), p.5220-5220

2016

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Abstract 5220: Evaluation of ACMG guideline classified variants in 180 cancer and incidental non-cancer genes in families with breastovarian cancer

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (14_Supplement), p.5220-5220

2016

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Abstract 5229: Pathogenic germline mutations and risk of multiple myeloma

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.5229-5229

2023

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11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood

4.7 - RF-to-dc Energy Conversion in Beam-Type Devices

566 IDENTIFICATION OF GENETIC MARKERS ASSOCIATED WITH RESPONSE TO BACILLUS CALMETTE-GUÉRIN INTRAVESICAL THERAPY IN NON-MUSCLE-INVASIVE BLADDER CANCER

915 EXOME SEQUENCING OF EXTREME PHENOTYPES TO IDENTIFY VARIANTS PREDICTIVE OF RESPONSE TO CHEMOTHERAPY IN BLADDER CANCER

995 ANALYSIS OF STATIN MEDICATION, GENETIC VARIATION AND PROSTATE CANCER OUTCOMES

995 ANALYSIS OF STATIN MEDICATION, GENETIC VARIATION AND PROSTATE CANCER OUTCOMES

Abstract 1281: Germline mutations in NBN conferring DNA damage response defects are found in patients with multiple cancer types

Abstract 1291: High and moderate penetrance germline mutations in a number of genes are responsible for a small proportion of familial breast cancer risk in BRCAx families

Abstract 1318: A genome-wide association study of Waldenström macroglobulinemia/lymphoplasmacytic lymphoma demonstrates association with chromosome 6

Abstract 1572: Inherited truncating RAD52 variant discovered using integrated germline- somatic analysis predicts clinical outcome in patients with lung cancers

Abstract 2033: Germline mutations in ETV6 confer risk of thrombocytopenia and acute lymphocytic leukemia

Abstract 221: Inherited variants at 3q13.33 and 3p24.1 influences risk of diffuse large B-cell lymphoma

Abstract 2378: Harmonization of next generation sequencing data within consortia for gene discovery in familial breast cancer

Abstract 2600: SLX4 mutation in hereditary breast cancer

Abstract 2742: Potential burden of germline findings in targeted tumor sequencing using matched normal DNA

Abstract 3258: Preclinical evaluation of enhanced irofulven antitumor activity in an ERCC3 mutant background by in vitro and in vivo tumor models

Abstract 3282: Determination of cancer susceptibility in probands with breast and ovarian cancer

Abstract 4265: Risks of familial breast cancer associated with known and proposed breast cancer susceptibility genes

Abstract 4280: FH (rs367543046, chr1:241661227 A/ATTT) heterozygous carrier status does not confer risk to hereditary leiomyomatosis and renal cell cancer (HLRCC) and prostate cancer

Abstract 4626: Genetic susceptibility to diffuse large B-cell lymphoma in a pooled study of three Eastern Asian populations

Abstract 5071: A genome-wide association study suggests evidence of variants at 6p21.32 associated with marginal zone lymphoma

Abstract 5072: Meta-analysis of genome-wide association studies identifies novel susceptibility loci for follicular lymphoma

Abstract 5220: Evaluation of ACMG guideline classified variants in 180 cancer and incidental non-cancer genes in families with breast/ovarian cancer

Abstract 5220: Evaluation of ACMG guideline classified variants in 180 cancer and incidental non-cancer genes in families with breastovarian cancer

Abstract 5229: Pathogenic germline mutations and risk of multiple myeloma

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