Cargando…

Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition

Hereditary predisposition to cancer concerns between 5% and 10% of cancers. The main genes involved in the most frequent syndromes (hereditary breast and ovarian cancer syndrome, hereditary nonpolyposis colorectal cancer syndrome) were identified in the 1990s. Exploration of their functional pathway...

Descripción completa

Detalles Bibliográficos
Autores principales:	Cavaillé, Mathias, Uhrhammer, Nancy, Privat, Maud, Ponelle‐Chachuat, Flora, Gay‐Bellile, Mathilde, Lepage, Mathis, Molnar, Ioana, Viala, Sandrine, Bidet, Yannick, Bignon, Yves‐Jean
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons, Inc. 2020
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756731/ https://www.ncbi.nlm.nih.gov/pubmed/33099839 http://dx.doi.org/10.1002/gcc.22911

Ejemplares similares

Feedback of extended panel sequencing in 1530 patients referred for suspicion of hereditary predisposition to adult cancers
por: Cavaillé, Mathias, et al.
Publicado: (2020)

Detection Rate and Spectrum of Pathogenic Variations in a Cohort of 83 Patients with Suspected Hereditary Risk of Kidney Cancer
por: Ouedraogo, Zangbéwendé Guy, et al.
Publicado: (2023)

Early Onset Multiple Primary Tumors in Atypical Presentation of Cowden Syndrome Identified by Whole-Exome-Sequencing
por: Cavaillé, Mathias, et al.
Publicado: (2018)

Case Series of 11 CDH1 Families (47 Carriers) Including Incidental Findings, Signet Ring Cell Colon Cancer and Review of the Literature
por: Lepage, Mathis, et al.
Publicado: (2023)

Rare duplication of the CDC73 gene and atypical hyperparathyroidism‐jaw tumor syndrome: A case report and review of the literature
por: Garrigues, Guilhaume, et al.
Publicado: (2023)

Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature
por: Cavaillé, Mathias, et al.
Publicado: (2023)

Is BRCA2 involved in early onset colorectal cancer risk?
por: Gay‐Bellile, Mathilde, et al.
Publicado: (2019)

A high expression ratio of RhoA/RhoB is associated with the migratory and invasive properties of basal-like Breast Tumors
por: Privat, Maud, et al.
Publicado: (2020)

Association between hereditary predisposition to common cancers and congenital multimalformations
por: Kwiatkowski, Fabrice, et al.
Publicado: (2019)

Improved Efficiency and Reliability of NGS Amplicon Sequencing Data Analysis for Genetic Diagnostic Procedures Using AGSA Software
por: Poulet, Axel, et al.
Publicado: (2016)

Antioxydation And Cell Migration Genes Are Identified as Potential Therapeutic Targets in Basal-Like and BRCA1 Mutated Breast Cancer Cell Lines
por: Privat, Maud, et al.
Publicado: (2018)

CHEK2 contribution to hereditary breast cancer in non-BRCA families
por: Desrichard, Alexis, et al.
Publicado: (2011)

BRCA Mutations Increase Fertility in Families at Hereditary Breast/Ovarian Cancer Risk
por: Kwiatkowski, Fabrice, et al.
Publicado: (2015)

PERCEPTION Trial protocol: Comparison of predictive and prognostic capacities of neutrophil, lymphocyte, and platelet counts and tumor-infiltrating lymphocytes in triple negative breast cancer
por: Lusho, Sejdi, et al.
Publicado: (2020)

Identification of miR-10b, miR-26a, miR-146a and miR-153 as potential triple-negative breast cancer biomarkers
por: Fkih M’hamed, Insaf, et al.
Publicado: (2015)

Hereditary Predisposition in Phthisis
Publicado: (1902)

Hereditary Predisposition in Phthisis
por: Miller, J. W.
Publicado: (1907)

Hereditary Predisposition to Dipsomania
por: Thomson, J. B.
Publicado: (1858)

ERCC1 and telomere status in breast tumours treated with neoadjuvant chemotherapy and their association with patient prognosis
por: Gay‐Bellile, Mathilde, et al.
Publicado: (2016)

Hereditary Predispositions to Myelodysplastic Syndrome
por: Bannon, Sarah A., et al.
Publicado: (2016)

The Influence of Hereditary Predisposition in Epilepsy
por: Russell, William
Publicado: (1889)

XENOBREAST Trial: A prospective study of xenografts establishment from surgical specimens of patients with triple negative or luminal b breast cancer
por: Veyssière, Hugo, et al.
Publicado: (2021)

Recurrence biomarkers of triple negative breast cancer treated with neoadjuvant chemotherapy and anti-EGFR antibodies
por: Radosevic-Robin, Nina, et al.
Publicado: (2021)

Strong Hereditary Predispositions to Colorectal Cancer
por: Hryhorowicz, Szymon, et al.
Publicado: (2022)

BRACAVENIR: an observational study of expectations and coping in young women with high hereditary risk of breast and ovarian cancer
por: Kwiatkowski, Fabrice, et al.
Publicado: (2019)

TERT promoter status and gene copy number gains: effect on TERT expression and association with prognosis in breast cancer
por: Gay-Bellile, Mathilde, et al.
Publicado: (2017)

Physiological TLR4 regulation in human fetal membranes as an explicative mechanism of a pathological preterm case
por: Belville, Corinne, et al.
Publicado: (2022)

BRACAVENIR - impact of a psychoeducational intervention on expectations and coping in young women (aged 18–30 years) exposed to a high familial breast/ovarian cancer risk: study protocol for a randomized controlled trial
por: Kwiatkowski, Fabrice, et al.
Publicado: (2016)

849. Reduced CIED Infections with an Antibacterial Envelope: Microbiologic Analysis of the WRAP-IT Study
por: Sohail, Muhammad R, et al.
Publicado: (2019)

Pancreatic cancer as a sentinel for hereditary cancer predisposition
por: Young, Erin L., et al.
Publicado: (2018)

Diagnosing hereditary cancer predisposition in men with prostate cancer
por: Pritzlaff, Mary, et al.
Publicado: (2020)

Genitourinary manifestations of hereditary cancer predisposition syndromes in children
por: Gillespie, Nali Julia, et al.
Publicado: (2020)

Hereditary Predisposition to Acute Myeloid Leukemia in Older Adults
por: Fenwarth, Laurène, et al.
Publicado: (2021)

Identification of a novel pathogenic variant in PALB2 and BARD1 genes by a multigene sequencing panel in triple negative breast cancer in Morocco
por: Laraqui, Abdelilah, et al.
Publicado: (2021)

MicroRNAs 146a and 147b Biomarkers for Colorectal Tumor's Localization
por: Omrane, Inés, et al.
Publicado: (2014)

The Content and Nature of Narrative Comments on Swiss Physician Rating Websites: Analysis of 849 Comments
por: McLennan, Stuart
Publicado: (2019)

POS-849 CHARACTERISTICS AND OUTCOMES OF HOSPITALIZED COVID-19 PATIENTS WITH ACUTE KIDNEY INJURY
por: ESCUDERO, A.E., et al.
Publicado: (2022)

Hereditary Predisposition to Prostate Cancer: From Genetics to Clinical Implications
por: Brandão, Andreia, et al.
Publicado: (2020)

Assessment of Risk of Hereditary Predisposition in Patients With Melanoma and/or Mesothelioma and Renal Neoplasia
por: Gupta, Sounak, et al.
Publicado: (2021)

Altered lipid accumulation in Nannochloropsis salina CCAP849/3 following EMS and UV induced mutagenesis
por: Beacham, T.A., et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_0taea3d3f2ajg5m4iqs6bkv9jj