Works matching DE "HEREDITARY cancer syndromes"

Results: 1102

Susceptibility to Breast Cancer: Hereditary Syndromes and Low Penetrance Genes.

Published in:

Breast Disease, 2007, v. 27, n. 1, p. 21

By:

Peshkin, Beth N.;
Nusbaum, Rachel;
Vogel, Kristen J.;
Ready, Kaylene

Publication type:

Article

Breast Cancer Risk Assessment and Genetic Testing: Complexities, Conundrums, and Community.

Published in:

Breast Disease, 2007, v. 27, n. 1, p. 1, doi. 10.3233/BD-2007-27101

By:

Peshkin, Beth N.

Publication type:

Article

Recent advances in pediatric colorectal cancer: a systematic review.

Published in:

Pediatric Surgery International, 2025, v. 41, n. 1, p. 1, doi. 10.1007/s00383-025-06076-w

By:

Dhoat, Navdeep;
Sharma, Shilpa

Publication type:

Article

Early-Onset Sarcoma With Germline MAX Variant: Expanding the Spectrum in Hereditary Pheochromocytoma and Paraganglioma Open Access.

Published in:

JCEM Case Reports, 2025, v. 3, n. 7, p. 1, doi. 10.1210/jcemcr/luaf119

By:

Eren, Aysegul;
Brock, Pamela L;
Dedhia, Priya H

Publication type:

Article

Constitutional Mismatch Repair Deficiency, the Most Aggressive Cancer Predisposition Syndrome : Clinical Presentation, Surveillance, and Management.

Published in:

Journal of Korean Neurosurgical Society, 2025, v. 68, n. 3, p. 294, doi. 10.3340/jkns.2025.0024

By:

Kang, Eungu;
Suh, Jin Kyung;
Kim, Sang-Dae

Publication type:

Article

Dual Inhibition of HIF-1α and HIF-2α as a Promising Treatment for VHL-Associated Hemangioblastomas: A Pilot Study Using Patient-Derived Primary Cell Cultures.

Published in:

Biomedicines, 2025, v. 13, n. 5, p. 1234, doi. 10.3390/biomedicines13051234

By:

Perona-Moratalla, Ana B.;
Carrión, Blanca;
Villar Gómez de las Heras, Karina;
Arias-Salazar, Lourdes;
Yélamos-Sanz, Blanca;
Segura, Tomás;
Serrano-Heras, Gemma

Publication type:

Article

A Multi‐Level Analysis of Barriers and Promoting Factors to Cascade Screening Uptake Among Male Relatives of BRCA1/2 Carriers: A Qualitative Study.

Published in:

Psycho-Oncology, 2025, v. 34, n. 5, p. 1, doi. 10.1002/pon.70160

By:

Ongaro, G.;
Hamilton, J. G.;
Groner, V.;
Hay, J. L.;
Calvello, M.;
Oliveri, S.;
Bonanni, B.;
Feroce, I.;
Pravettoni, G.

Publication type:

Article

Constitutional Mismatch Repair Deficiency: Scoping Review of a Cancer‐Predisposition Syndrome With Distinctive Cutaneous Findings.

Published in:

Pediatric Dermatology, 2025, v. 42, n. 3, p. 437, doi. 10.1111/pde.15878

By:

Mar, Kristie;
Ameri, Kimia;
Lam, Joseph M.

Publication type:

Article

Germinal pathogenic CHEK2, novel APC and somatic JAK2V617F variants in a young patient with colorectal cancer, atypical leukemia, cerebral tumour and aggressive course.

Published in:

Ecancermedicalscience, 2025, v. 19, n. 1824-1915, p. 1, doi. 10.3332/ecancer.2025.1833

By:

Rodriguez Rojas, Lisa Ximena;
Olave Rodriguez, Jorge Andrés;
Bonilla Navarrete, Sebastián;
Valentina Carvajal, Laura;
Albán Silva, Juan José;
Doza Martínez, Liliana;
Nastasi Catanese, Jose Antonio

Publication type:

Article

The Jeter/Kohlmann/Gruber Article Reviewed.

Published in:

Oncology (08909091), 2006, v. 20, n. 3, p. 286

By:

Burt, Randall W.

Publication type:

Article

The Jeter/Kohlmann/Gruber Article Reviewed.

Published in:

Oncology (08909091), 2006, v. 20, n. 3, p. 285

By:

Offit, Kenneth

Publication type:

Article

Radiation-induced tumors and secondary malignancies following radiotherapy.

Published in:

Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2022, v. 79, n. 7, p. 643, doi. 10.2298/VSP201210017D

By:

Dedović Stojaković, Jelena;
Jovanović, Luka;
Filipović, Predrag;
Marinković, Tamara;
Marinković, Mladen;
Vujanac, Vukač;
Plešinac Karapandžić, Vesna

Publication type:

Article

Transfer of embryos with positive results following preimplantation genetic testing for monogenic disorders (PGT-M): experience of two high-volume fertility clinics.

Published in:

Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 9, p. 1949, doi. 10.1007/s10815-019-01538-2

By:

Besser, Andria G.;
Blakemore, Jennifer K.;
Grifo, James A.;
Mounts, Emily L.

Publication type:

Article

King for a Year.

Published in:

Bio-IT World, 2004, v. 3, n. 11, p. 20

By:

Davies, Kevin

Publication type:

Article

Von Hippel-Lindau syndrome: clinical features, genetic foundations, and management strategies.

Published in:

Molecular Biology Reports, 2025, v. 52, n. 1, p. 1, doi. 10.1007/s11033-025-10403-8

By:

Harbi, Emirhan;
Aschner, Michael

Publication type:

Article

Protein kinase C iota (PKCι) and pVHL are both needed for lysosomal degradation of α5 integrin in renal carcinoma cells.

Published in:

Molecular Biology Reports, 2025, v. 52, n. 1, p. 1, doi. 10.1007/s11033-025-10272-1

By:

Schurr, Alissa F.;
Dave, Chandni S.;
Shah, Prachi J.;
Meth, Jennifer L.;
Jaramillo, Alexandria S.;
Bartley, Kelly;
Schoenfeld, Alan R.

Publication type:

Article

Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: Identification of novel and recurrent deletions by MLPA(Communicated by Richard Cotton).

Published in:

Human Mutation, 2003, v. 22, n. 6, p. 428, doi. 10.1002/humu.10291

By:

C.F. Taylor;
R.S. Charlton;
J. Burn;
E. Sheridan

Publication type:

Article

Insights into the molecular features of the von Hippel–Lindau-like protein.

Published in:

Amino Acids, 2019, v. 51, n. 10-12, p. 1461, doi. 10.1007/s00726-019-02781-8

By:

Minervini, Giovanni;
Quaglia, Federica;
Tabaro, Francesco;
Tosatto, Silvio C. E.

Publication type:

Article

Cancer Risk Assessment and the Genetic Counseling Process: Using Hereditary Breast and Ovarian Cancer as an Example.

Published in:

Medical Principles & Practice, 2008, v. 17, n. 3, p. 173, doi. 10.1159/000117790

By:

Prucka, Sandra K.;
McIlvried, Dawn E.;
Korf, Bruce R.

Publication type:

Article

Increased Number of Colorectal Interval Cancers in Lynch Syndrome after the SARS-CoV-2 Pandemic: A Survey-Based Study.

Published in:

Digestive Diseases, 2023, v. 41, n. 2, p. 227, doi. 10.1159/000524393

By:

Russo, Michele;
Barchi, Alberto;
Mannucci, Alessandro;
Puzzono, Marta;
Zuppardo, Raffaella Alessia;
Biamonte, Paolo;
Bencardino, Sarah;
Leandro, Gioacchino;
Cannizzaro, Renato;
Monica, Fabio;
Zagari, Rocco Maurizio;
Pasquale, Luigi;
Goni, Elisabetta;
Di Leo, Milena;
Ricciardiello, Luigi;
Cavestro, Giulia Martina

Publication type:

Article

THE ALARMING SURGE OF EARLY ONSET COLORECTAL CANCER: A CALL FOR EARLY DETECTION AND PREVENTATIVE MEASURES.

Published in:

Turkish Medical Student Journal, 2025, v. 12, n. 1, p. 1, doi. 10.4274/tmsj.galenos.2025.2024-10-3

By:

Tenekeci, Ateş Kutay;
Ünal, Ahmet Arda;
Çeltikçi, Başak

Publication type:

Article

Referral challenges for early-onset colorectal cancer: a qualitative study in UK primary care.

Published in:

BJGP Open, 2023, v. 7, n. 4, p. 1, doi. 10.3399/BJGPO.2023.0123

By:

O'Neill, Orla M.;
Coleman, Helen G.;
Reid, Helen

Publication type:

Article

Potential pathogenic germline variant reporting from tumor comprehensive genomic profiling complements classic approaches to germline testing.

Published in:

NPJ Precision Oncology, 2023, v. 7, n. 1, p. 1, doi. 10.1038/s41698-023-00429-1

By:

Tung, Nadine;
Dougherty, Kali Chatham;
Gatof, Emily Stern;
DeLeonardis, Kim;
Hogan, Lauren;
Tukachinsky, Hanna;
Gornstein, Erica;
Oxnard, Geoffrey R.;
McGregor, Kimberly;
Keller, Rachel B.

Publication type:

Article

THERAPEUTICAL TARGETS IN BREAST CANCER: ESR1 AND BRCA1 MUTATIONS.

Published in:

Genetics & Applications, 2023, p. 73

By:

Dalila, Žilić;
Amina, Kurtović-Kozarić

Publication type:

Article

THE ROLE OF GENETICS IN THE DISCOVERY OF CANCER TREATMENTS.

Published in:

Genetics & Applications, 2023, p. 19

By:

Amina, Kurtović-Kozarić

Publication type:

Article

Strategies to Assess Risk for Hereditary Cancer in Primary Care Clinics: A Cluster Randomized Clinical Trial.

Published in:

JAMA Network Open, 2025, v. 8, n. 3, p. e250185, doi. 10.1001/jamanetworkopen.2025.0185

By:

Swisher, Elizabeth M.;
Harris, Heather M.;
Knerr, Sarah;
Theoryn, Tesla N.;
Norquist, Barbara M.;
Brant, Jeannine;
Shirts, Brian H.;
Beers, Faith;
Cameron, DaLaina;
Dusic, Emerson J.;
Riemann, Laurie A.;
Devine, Beth;
Raff, Michael L.;
Kadel, Rabindra;
Cabral, Howard J.;
Wang, Catharine

Publication type:

Article

Clinician-Reported Impact of Germline Multigene Panel Testing on Cancer Risk Management Recommendations.

Published in:

JNCI Cancer Spectrum, 2022, v. 6, n. 2, p. 1, doi. 10.1093/jncics/pkac002

By:

Horton, Carolyn;
Blanco, Kirsten;
Lo, Min-Tzu;
Speare, Virginia;
LaDuca, Holly;
Dolinsky, Jill S;
Kurian, Allison W

Publication type:

Article

Double Hit in Clear-Cell Renal Cell Carcinoma With Germline Pathogenic ATM Mutation and Somatic VHL Mutation.

Published in:

Journal of Investigative Medicine High Impact Case Reports, 2024, p. 1, doi. 10.1177/23247096241286370

By:

Chan, Kok Hoe;
Clavijo, Nicolas Duque;
Ayala, Gustavo;
Hall, Ryan;
Wray, Curtis;
Cen, Putao

Publication type:

Article

Hereditary leiomyomatosis and renal cell carcinoma/fumarate hydratase‐deficient renal cell carcinoma: two primaries in one.

Published in:

ANZ Journal of Surgery, 2020, v. 90, n. 4, p. E93, doi. 10.1111/ans.15323

By:

Storey, Benjamin;
Shugg, Nathan;
Grant, Alexander

Publication type:

Article

Clinical implications of the genetics of sporadic colorectal cancer.

Published in:

ANZ Journal of Surgery, 2019, v. 89, n. 10, p. 1224, doi. 10.1111/ans.15074

By:

Fischer, Jesse;
Walker, Logan C.;
Robinson, Bridget A.;
Frizelle, Frank A.;
Church, James M.;
Eglinton, Tim W.

Publication type:

Article

Cancer in Māori: lessons from prostate, colorectal and gastric cancer and progress in hereditary stomach cancer in New Zealand.

Published in:

ANZ Journal of Surgery, 2013, v. 83, n. 1/2, p. 42, doi. 10.1111/ans.12042

By:

Blair, Vanessa;
Kahokehr, Arman;
Sammour, Tarik

Publication type:

Article

Evaluation of Neurofibromatosis Gene Expression in Non-Hereditary Breast Cancer.

Published in:

Novelty in Biomedicine, 2023, v. 11, n. 1, p. 16

By:

Kavousi, Mahsa;
Smailzadeh, Fatemeh;
Mehrabadi, Jalil Fallah;
Geranpayeh, Lobat

Publication type:

Article

Current status and perspectives of genetic testing in gastrointestinal cancer (Review).

Published in:

Oncology Letters, 2024, v. 27, n. 1, p. N.PAG, doi. 10.3892/ol.2023.14155

By:

Matsuoka, Tasuku;
Yashiro, Masakazu

Publication type:

Article

Improving the overall diagnostic rate of early gastric cancer by managing family members with hereditary cancer syndromes.

Published in:

Oncology Letters, 2020, v. 20, n. 6, p. N.PAG, doi. 10.3892/ol.2020.12158

By:

Zhang, Hao

Publication type:

Article

Downregulation of ZNF365 by methylation predicts poor prognosis in patients with colorectal cancer by decreasing phospho-p53 (Ser15) expression.

Published in:

Oncology Letters, 2020, v. 20, n. 4, p. N.PAG, doi. 10.3892/ol.2020.11946

By:

Wang, Chan;
Liu, Shuiping;
Kuang, Yeye;
Hu, Xiaotong;
Fang, Xiao

Publication type:

Article

Novel loss-of-function mutation in BRCA2 gene identified in a Chinese female with a family history of ovarian cancer: A case report.

Published in:

Oncology Letters, 2019, v. 17, n. 3, p. 3350

By:

Cui, Yanzhi;
Wang, Yanyan;
Zhang, Ningzhi;
He, Jun;
Huang, Hui;
Liu, Fengling;
Wei, Suju;
Dong, Qian;
Wu, Jing;
Lin, Keke;
Chen, Weixi;
Xiang, Jiale;
Jin, Hui;
Peng, Zhiyu;
Zhao, Qiang;
Li, Wei;
Jiang, Da;
Banerjee, Santasree

Publication type:

Article

BRCA1 mutation in breast cancer patients: Analysis of prognostic factors and survival.

Published in:

Oncology Letters, 2019, v. 17, n. 2, p. 1986

By:

Huszno, Joanna;
Kołosza, Zofia;
Grzybowska, Ewa

Publication type:

Article

Diaphragmatic clear cell carcinoma with Lynch syndrome after surgery for atypical endometrial hyperplasia and ovarian endometriosis: A case report.

Published in:

2024

By:

Ueda, Makiko;
Watanabe, Takafumi;
Momma, Tomoyuki;
Kanke, Yasuyuki;
Kato, Asami;
Okabe, Chikako;
Sato, Tetsu;
Kamo, Norihito;
Endo, Yuta;
Furukawa, Shigenori;
Soeda, Shu;
Fujimori, Keiya

Publication type:

Case Study

Relationship between MUTYH, OGG1 and BRCA1 mutations and mRNA expression in breast and ovarian cancer predisposition.

Published in:

Molecular & Clinical Oncology, 2021, v. 14, n. 1, p. N.PAG

By:

Moscatello, Carmelo;
Di Nicola, Marta;
Veschi, Serena;
Di Gregorio, Patrizia;
Cianchetti, Ettore;
Stuppia, Liborio;
Battista, Pasquale;
Cama, Alessandro;
Curia, Maria Cristina;
Aceto, Gitana Maria

Publication type:

Article

PALB2 mutation in a woman with bilateral breast cancer: A case report.

Published in:

Molecular & Clinical Oncology, 2017, v. 6, n. 4, p. 556, doi. 10.3892/mco.2017.1189

By:

HIROSHI NAKAGOMI;
YOSUKE HIROTSU;
KENICHIRO OKIMOTO;
IKUKO SAKAMOTO;
KENJI AMEMIYA;
SATOKO NAKAGOMI;
TAKEO KUBOTA;
HITOSHI MOCHIZUKI;
MASAO OMATA

Publication type:

Article

Deficient immune function of peripheral blood mononuclear cells from patients with Gardner syndrome.

Published in:

Clinical & Experimental Immunology, 1985, v. 60, n. 3, p. 525

By:

Warren, R. P.;
Stembridge, A. M.;
Gardner, E. J.

Publication type:

Article

A New MEN2 Syndrome with Clinical Features of Both MEN2A and MEN2B Associated with a New RET Germline Deletion.

Published in:

Case Reports in Endocrinology, 2020, p. 1, doi. 10.1155/2020/4147097

By:

Giani, Carlotta;
Ramone, Teresa;
Romei, Cristina;
Ciampi, Raffaele;
Tacito, Alessia;
Valerio, Laura;
Agate, Laura;
Ugolini, Clara;
Marinò, Michele;
Basolo, Fulvio;
Franchi, Alessandro;
Borsari, Simona;
Michelucci, Angela;
Selli, Cesare;
Materazzi, Gabriele;
Cetani, Filomena;
Elisei, Rossella

Publication type:

Article

Preferences for Genetic Testing to Predict the Risk of Developing Hereditary Cancer: A Systematic Review of Discrete Choice Experiments.

Published in:

Medical Decision Making, 2024, v. 44, n. 3, p. 252, doi. 10.1177/0272989X241227425

By:

Morrish, N.;
Snowsill, T.;
Dodman, S.;
Medina-Lara, A.

Publication type:

Article

Mechanistic Targets and Nutritionally Relevant Intervention Strategies to Break Obesity–Breast Cancer Links.

Published in:

Frontiers in Endocrinology, 2021, v. 11, p. N.PAG, doi. 10.3389/fendo.2021.632284

By:

Bustamante-Marin, Ximena M.;
Merlino, Jenna L.;
Devericks, Emily;
Carson, Meredith S.;
Hursting, Stephen D.;
Stewart, Delisha A.

Publication type:

Article

Mechanistic Targets and Nutritionally Relevant Intervention Strategies to Break Obesity--Breast Cancer Links.

Published in:

Frontiers in Endocrinology, 2021, v. 11, p. 1, doi. 10.3389/fendo.2021.632284

By:

Bustamante-Marin, Ximena M.;
Merlino, Jenna L.;
Devericks, Emily;
Carson, Meredith S.;
Hursting, Stephen D.;
Stewart, Delisha A.

Publication type:

Article

Whole Genome Sequencing Prioritizes CHEK2, EWSR1 , and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer.

Published in:

Frontiers in Endocrinology, 2021, v. 11, p. N.PAG, doi. 10.3389/fendo.2021.600682

By:

Srivastava, Aayushi;
Giangiobbe, Sara;
Skopelitou, Diamanto;
Miao, Beiping;
Paramasivam, Nagarajan;
Diquigiovanni, Chiara;
Bonora, Elena;
Hemminki, Kari;
Försti, Asta;
Bandapalli, Obul Reddy

Publication type:

Article

Incidental Serous Tubal Intraepithelial Carcinoma that Developed into Primary Peritoneal Serous Carcinoma in a Patient without BRCA Mutation.

Published in:

American Journal of Case Reports, 2020, v. 21, p. 1, doi. 10.12659/AJCR.921146

By:

Gun Oh Chong;
Ji Young Park;
Hyun Jung Lee

Publication type:

Article

GENETIC CONSIDERATIONS OF DISEASES AND DISORDERS THAT AFFECT ORAL CAVITY.

Published in:: Oral Health (0974-3960), 2020, v. 14, n. 10, p. 22
Publication type:: Article

Genetic Features of Tumours Arising in the Context of Suspected Hereditary Cancer Syndromes with RAD50 , RAD51C/D , and BRIP1 Germline Mutations, Results of NGS-Reanalysis of BRCA/MMR-Negative Families.

Published in:

Genes, 2025, v. 16, n. 4, p. 458, doi. 10.3390/genes16040458

By:

Arranz-Ledo, Mónica;
Infante, Mar;
Lastra, Enrique;
Olaverri, Amaya;
Orozco, Marta;
Mateo, Lucia C.;
Martínez, Noemí;
Hernández, Lara;
Durán, Mercedes

Publication type:

Article

Constitutional Mutation of PIK3CA : A Variant of Cowden Syndrome?

Published in:

2024

By:

Vida-Navas, Elena;
Barca-Tierno, Verónica;
López-Gómez, Victoria;
Salazar, María Teresa;
Moreno-Pelayo, Miguel A.;
Guillén-Ponce, Carmen

Publication type:

Case Study