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1. Full Text Molecular pathways: Fumarate Hydratase-deficient kidney cancer - Targeting the warburg effect in cancer
by Linehan, W. Marston and Rouault, Tracey A
Clinical cancer research, ISSN 1078-0432, 07/2013, Volume 19, Issue 13, pp. 3345 - 3352
Life Sciences & Biomedicine | Oncology | Science & Technology | Tumors of the urinary system | Kidneys | Pharmacology. Drug treatments | Nephrology. Urinary tract diseases | Biological and medical sciences | Multiple tumors. Solid tumors. Tumors in childhood (general aspects) | Medical sciences | Antineoplastic agents | Tumors | Uterine Neoplasms - genetics | AMP-Activated Protein Kinases - metabolism | Uterine Neoplasms - metabolism | Skin Neoplasms - drug therapy | Humans | Translational Medical Research | Leiomyomatosis - metabolism | Antineoplastic Agents - therapeutic use | Fumarate Hydratase - deficiency | Fumarate Hydratase - genetics | Molecular Targeted Therapy | Neoplastic Syndromes, Hereditary | Skin Neoplasms - metabolism | Fumarate Hydratase - metabolism | Basic Helix-Loop-Helix Transcription Factors - metabolism | Signal Transduction - drug effects | Leiomyomatosis - drug therapy | Skin Neoplasms - genetics | Uterine Neoplasms - drug therapy | Antineoplastic Agents - pharmacology | Leiomyomatosis - genetics | Index Medicus
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2. Full Text “It’s not if I get cancer, it’s when I get cancer”: BRCA-positive patients’ (un)certain health experiences regarding hereditary breast and ovarian cancer risk
by Dean, Marleah
Social science & medicine (1982), ISSN 0277-9536, 08/2016, Volume 163, pp. 21 - 27
BRCA | Genetic risk | Hereditary breast and ovarian cancer | Communication | Public, Environmental & Occupational Health | Social Sciences | Life Sciences & Biomedicine | Biomedical Social Sciences | Social Sciences, Biomedical | Science & Technology | Decision Making | Genetic Predisposition to Disease - psychology | Ovarian Neoplasms - psychology | Risk Assessment - methods | Uncertainty | Humans | Middle Aged | Ovarian Neoplasms - genetics | Breast Neoplasms - genetics | Breast Neoplasms - psychology | Texas | Genes, BRCA2 | Adult | Female | Genes, BRCA1 | Women - psychology | Risk Assessment - standards | Development and progression | Breast cancer | Genetic aspects | Health aspects | Risk factors | Ovarian cancer | Health | Certainty | Attitudes | Risk | Mothers | Patients | Trauma | Medicine | Womens health | Risk assessment | Genetics | Internet | Mass media | Genetic testing | Mutation | Females | Cancer | Index Medicus
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3. Genetic disorders sourcebook
: basic consumer health information about heritable disorders, including disorders resulting from abnormalities in specific genes, such as hemophilia, sickle cell disease, and cystic fibrosis, chromosomal disorders, such as down syndrome, fragile x syndrome, and klinefelter syndrome, and complex disorders with environmental and genetic components, such as alzheimer disease, cancer, heart disease, and obesity; along with information about the human genome project, genetic testing and newborn screen
by Judd, Sandra J
2014, 5th edition., Health reference series, ISBN 0780813014, xxi, 716
Human chromosome abnormalities
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4. Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial colorectal cancer type X
by Lindor, Noralane M and Rabe, Kari and Petersen, Gloria M and Haile, Robert and Casey, Graham and Baron, John and Gallinger, Steve and Bapat, Bharati and Aronson, Melyssa and Hopper, John and Jass, Jeremy and LeMarchand, Loic and Grove, John and Potter, John and Newcomb, Polly and Terdiman, Jonathan P and Conrad, Peggy and Moslein, Gabriella and Goldberg, Richard and Ziogas, Argyrios and Anton-Culver, Hoda and De Andrade, Mariza and Siegmund, Kim and Thibodeau, Stephen N and Boardman, Lisa A and Seminara, Daniela
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 04/2005, Volume 293, Issue 16, pp. 1979 - 1985
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Colorectal Neoplasms, Hereditary Nonpolyposis - classification | MutL Protein Homolog 1 | Colorectal Neoplasms - genetics | Humans | Middle Aged | Male | DNA Repair - genetics | Base Pair Mismatch - genetics | Neoplastic Syndromes, Hereditary - epidemiology | Neoplasms - genetics | Adult | Female | Neoplastic Syndromes, Hereditary - genetics | Neoplasm Proteins - genetics | Chromosomal Instability | Microsatellite Repeats | Carrier Proteins | Colorectal Neoplasms - epidemiology | SEER Program | Risk Assessment | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Proto-Oncogene Proteins - genetics | Colorectal Neoplasms - classification | MutS Homolog 2 Protein | DNA-Binding Proteins - genetics | Mutation - genetics | Nuclear Proteins | Adaptor Proteins, Signal Transducing | Mass Screening | Colorectal Neoplasms, Hereditary Nonpolyposis - epidemiology | Pedigree | Heterozygote | Aged | Neoplastic Syndromes, Hereditary - classification | Neoplasms - epidemiology | Heredity | Health risk assessment | Genes | Deoxyribonucleic acid--DNA | Colorectal cancer
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5. Full Text Gynecologic Cancer as a “Sentinel Cancer” for Women With Hereditary Nonpolyposis Colorectal Cancer Syndrome
by Lu, Karen H and Dinh, Mai and Kohlmann, Wendy and Watson, Patrice and Green, Jane and Syngal, Sapna and Bandipalliam, Prathap and Chen, Lee-May and Allen, Brian and Conrad, Peggy and Terdiman, Jonathan and Sun, Charlotte and Daniels, Molly and Burke, Thomas and Gershenson, David M and Lynch, Henry and Lynch, Patrick and Broaddus, Russell R
Obstetrics and gynecology (New York. 1953), ISSN 0029-7844, 03/2005, Volume 105, Issue 3, pp. 569 - 574
Gastroenterology. Liver. Pancreas. Abdomen | Stomach. Duodenum. Small intestine. Colon. Rectum. Anus | Gynecology. Andrology. Obstetrics | Biological and medical sciences | Medical sciences | Tumors | Time Factors | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | Ovarian Neoplasms - diagnosis | Humans | Middle Aged | Adult | Female | Aged | Endometrial Neoplasms - diagnosis | Neoplasms, Multiple Primary - diagnosis | Neoplasms, Second Primary - diagnosis | Index Medicus | Abridged Index Medicus
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6. Full Text Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment
by Menko, F.H and Maher, E.R and Schmidt, L.S and Middelton, L.A and Aittomaki, K and Tomlinson, I and Richard, S and Linehan, W
Familial cancer, ISSN 1389-9600, 2014, Volume 13, Issue 4, pp. 637 - 644
Human Genetics | Tricarboxylic acid cycle | Fumarate hydratase | Biomedicine | Surveillance | Nephrectomy | Targeted therapy | Hereditary leiomyomatosis and renal cell cancer | Cancer Research | Type 2 papillary renal cell cancer | Epidemiology | Biomedicine general | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Kidney Neoplasms - genetics | Early Detection of Cancer - methods | Humans | Middle Aged | Carcinoma, Renal Cell - genetics | Male | Kidney Neoplasms - diagnosis | Neoplastic Syndromes, Hereditary | Skin Neoplasms - complications | Leiomyomatosis - complications | Carcinoma, Renal Cell - diagnosis | Uterine Neoplasms - complications | Female | Enzymes | Medical genetics | Genetic aspects | Health aspects | Population genetics | Risk factors | Cancer | Index Medicus | targeted therapy | tricarboxylic acid cycle | fumarate hydratase | nephrectomy | surveillance | hereditary leiomyomatosis and renal cell cancer | papillary type 2 renal cancer
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7. Full Text Hereditary colorectal cancer syndromes: American society of clinical oncology clinical practice guideline endorsement of familial risk-colorectal cancer: European Society for medical oncology clinical practice guidelines
by Stoffel, Elena M and Mangu, Pamela B and Gruber, Stephen B and Hamilton, Stanley R and Kalady, Matthew F and Lau, Michelle Wan Yee and Lu, Karen H and Roach, Nancy and Limburg, Paul J and European Society of Clinical Oncology and American Society of Clinical Oncology
Journal of clinical oncology, ISSN 0732-183X, 10/2015, Volume 33, Issue 2, pp. 209 - 217
Life Sciences & Biomedicine | Oncology | Science & Technology | Medical History Taking | Microsatellite Instability | Genetic Testing | Sigmoidoscopy | Early Detection of Cancer - methods | Adenomatous Polyposis Coli - prevention & control | Humans | Genetic Counseling | Colorectal Neoplasms, Hereditary Nonpolyposis - prevention & control | Colorectal Neoplasms, Hereditary Nonpolyposis - therapy | Anticarcinogenic Agents - administration & dosage | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | Colonoscopy | DNA Mismatch Repair | Germ-Line Mutation | Adenomatous Polyposis Coli - therapy | Adenomatous Polyposis Coli - genetics | Population Surveillance - methods | Adenomatous Polyposis Coli Protein - genetics | Genetic Predisposition to Disease | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | DNA Glycosylases - genetics | Heterozygote | Adenomatous Polyposis Coli - diagnosis | Chemoprevention - methods | Index Medicus | Gic2 | To4 | ASCO Special | Gic1 | To8 | Gdln1
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8. Full Text A study of over 35,000 women with breast cancer tested with a 25‐gene panel of hereditary cancer genes
by Buys, Saundra S and Sandbach, John F and Gammon, Amanda and Patel, Gayle and Kidd, John and Brown, Krystal L and Sharma, Lavania and Saam, Jennifer and Lancaster, Johnathan and Daly, Mary B
Cancer, ISSN 0008-543X, 05/2017, Volume 123, Issue 10, pp. 1721 - 1730
breast cancer type 1 (BRCA1) | panel testing | hereditary breast and ovarian cancer | BRCA2 | triple‐negative breast cancer | triple-negative breast cancer | Life Sciences & Biomedicine | Oncology | Science & Technology | Genetic Testing | Age Factors | Humans | Middle Aged | Young Adult | Checkpoint Kinase 2 - genetics | Tumor Suppressor Proteins - genetics | Aged, 80 and over | Genes, BRCA2 | Adult | Female | RNA Helicases - genetics | Lynch Syndrome II - genetics | Neoplastic Syndromes, Hereditary - genetics | Genes, BRCA1 | Nuclear Proteins - genetics | Fanconi Anemia Complementation Group N Protein | Hereditary Breast and Ovarian Cancer Syndrome - genetics | DNA-Binding Proteins - genetics | Fanconi Anemia Complementation Group Proteins | Breast Neoplasms - genetics | Triple Negative Breast Neoplasms - genetics | Aged | Ataxia Telangiectasia Mutated Proteins - genetics | Ubiquitin-Protein Ligases - genetics | Women | Breast cancer | Genetic aspects | Diagnosis | Research | Health aspects | Oncogenes | BRCA2 protein | CHK2 protein | Threonine | BRCA1 protein | Genes | Health risks | Protein C | Genetic screening | DNA helicase | Men | Ataxia | Ataxia telangiectasia mutated protein | Protein-serine/threonine kinase | Mutation | Health risk assessment | Age | Cancer | Index Medicus | Abridged Index Medicus
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9. Full Text Childhood cancer predisposition syndromes—A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
by Ripperger, Tim and Bielack, Stefan S and Borkhardt, Arndt and Brecht, Ines B and Burkhardt, Birgit and Calaminus, Gabriele and Debatin, Klaus‐Michael and Deubzer, Hedwig and Dirksen, Uta and Eckert, Cornelia and Eggert, Angelika and Erlacher, Miriam and Fleischhack, Gudrun and Frühwald, Michael C and Gnekow, Astrid and Goehring, Gudrun and Graf, Norbert and Hanenberg, Helmut and Hauer, Julia and Hero, Barbara and Hettmer, Simone and von Hoff, Katja and Horstmann, Martin and Hoyer, Juliane and Illig, Thomas and Kaatsch, Peter and Kappler, Roland and Kerl, Kornelius and Klingebiel, Thomas and Kontny, Udo and Kordes, Uwe and Körholz, Dieter and Koscielniak, Ewa and Kramm, Christof M and Kuhlen, Michaela and Kulozik, Andreas E and Lamottke, Britta and Leuschner, Ivo and Lohmann, Dietmar R and Meinhardt, Andrea and Metzler, Markus and Meyer, Lüder H and Moser, Olga and Nathrath, Michaela and Niemeyer, Charlotte M and Nustede, Rainer and Pajtler, Kristian W and Paret, Claudia and Rasche, Mareike and Reinhardt, Dirk and Rieß, Olaf and Russo, Alexandra and Rutkowski, Stefan and Schlegelberger, Brigitte and Schneider, Dominik and Schneppenheim, Reinhard and Schrappe, Martin and Schroeder, Christopher and von Schweinitz, Dietrich and Simon, Thorsten and Sparber‐Sauer, Monika and Spix, Claudia and Stanulla, Martin and Steinemann, Doris and Strahm, Brigitte and Temming, Petra and Thomay, Kathrin and von Bueren, Andre O and Vorwerk, Peter and Witt, Olaf and Wlodarski, Marcin and Wössmann, Willy and Zenker, Martin and Zimmermann, Stefanie and Pfister, Stefan M and Kratz, Christian P
American journal of medical genetics. Part A, ISSN 1552-4825, 04/2017, Volume 173, Issue 4, pp. 1017 - 1037
hereditary cancer syndrome | genetic predisposition testing | genetic screening | genetic cancer predisposition | germline mutation | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Hematologic Neoplasms - diagnosis | Gene Expression | Genetic Predisposition to Disease | Genetics, Medical - methods | History, 21st Century | Humans | Genetics, Medical - history | Hematologic Neoplasms - pathology | Neoplasms - diagnosis | Genetics, Medical - instrumentation | Focus Groups - methods | Genetic Counseling - ethics | Genetic Testing - methods | Syndrome | Societies, Medical - history | Neoplasms - genetics | Adolescent | Hematologic Neoplasms - genetics | Mutation | Neoplasm Proteins - genetics | Neoplasms - pathology | Child | Pediatrics | Cancer in children | Oncology | Society | Hematology | Cancer | Index Medicus
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