Cargando…

Targeted next-generation sequencing of 21 candidate genes in hereditary ovarian cancer patients from the Republic of Bashkortostan

About 5–10% of all ovarian cancer cases show familial clustering, and some 15–25% of familial ovarian cancer cases are mediated by high-penetrance mutations in the BRCA1 and BRCA2 genes. Only few other genes have been identified for familial ovarian cancer. We conducted targeted next-generation sequ...

Descripción completa

Detalles Bibliográficos
Autores principales:	Prokofyeva, D. S., Mingazheva, E. T., Valova, Ya. V., Sakaeva, D. D., Faishanova, R. R., Nurgalieva, A. Kh., Valiev, R. R., Bogdanova, N., Dörk, T., Khusnutdinova, E. K.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2023
Materias:	Brief Communication
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071671/ https://www.ncbi.nlm.nih.gov/pubmed/37013556 http://dx.doi.org/10.1186/s13048-023-01119-z

Ejemplares similares

Whole Exome Sequencing Study Suggests an Impact of FANCA, CDH1 and VEGFA Genes on Diffuse Gastric Cancer Development
por: Nurgalieva, Alfiia, et al.
Publicado: (2023)

Soil fertility analysis in the Republic of Bashkortostan
por: Mirsayapov, Ramil, et al.
Publicado: (2022)

A Splice Site Variant of CDK12 and Breast Cancer in Three Eurasian Populations
por: Bogdanova, Natalia V., et al.
Publicado: (2019)

Systemic juvenile idiopathic arthritis in the republic of Bashkortostan
por: Malievskiy, VA
Publicado: (2011)

Cost-effective horse breeding in the Republic of Bashkortostan, Russia
por: Askarov, Almir, et al.
Publicado: (2020)

Predicting Mortality by Causes in the Republic of Bashkortostan Using the Lee–Carter Model
por: Lakman, I. A., et al.
Publicado: (2021)

Genetic Polymorphisms of Cytochromes P450 in Finno-Permic Populations of Russia
por: Dzhaubermezov, Murat, et al.
Publicado: (2022)

Osteogenesis Imperfecta: Search for Mutations in Patients from the Republic of Bashkortostan (Russia)
por: Nadyrshina, Dina, et al.
Publicado: (2022)

Prevalence and incidence of juvenile idiopathic arthritis in children in the republic of Bashkortostan: the epidemiological study
por: Malievskiy, VA
Publicado: (2011)

Utilization of poultry manure when cultivating potatoes in the southern steppe of the Republic of Bashkortostan
por: Shafeeva, Elina, et al.
Publicado: (2022)

Studying the relationship between mental health literacy and emotional state among young people in Republic of Bashkortostan
por: Galyautdinova, S., et al.
Publicado: (2022)

Identification of promising alfalfa varieties in conditions of the southern forest-steppe zone (Republic of Bashkortostan): a study of economic and biological characteristics
por: Kuznetsov, Igor, et al.
Publicado: (2022)

Hereditary breast cancer: ever more pieces to the polygenic puzzle
por: Bogdanova, Natalia, et al.
Publicado: (2013)

Mutation Analysis of the ERCC4/FANCQ Gene in Hereditary Breast Cancer
por: Kohlhase, Sandra, et al.
Publicado: (2014)

Prevalence of depression, anxiety and suicidal ideas and associated factors, in particular sensory impairments, in a population of Bashkortostan in Russia
por: Bikbov, Mukharram M., et al.
Publicado: (2023)

Bioethical issues of preventing hereditary diseases with late onset in the Sakha Republic (Yakutia)
por: Kononova, Sardana K., et al.
Publicado: (2014)

Epidemiology of Hereditary Diseases in the Karachay-Cherkess Republic
por: Zinchenko, Rena A., et al.
Publicado: (2020)

Prevalence of and factors associated with low Back pain, thoracic spine pain and neck pain in Bashkortostan, Russia: the Ural Eye and Medical Study
por: Bikbov, Mukharram M., et al.
Publicado: (2020)

Molecular Genetics of Breast and Ovarian Cancer: Recent Advances and Clinical Implications
por: Bogdanova, N, et al.
Publicado: (2012)

Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing
por: Stanislaw, Christine, et al.
Publicado: (2016)

P1527: NEXT GENERATION SEQUENCING IN HEREDITARY SPHEROCYTOSIS DIAGNOSIS
por: García Feria, A., et al.
Publicado: (2022)

Genetic and Preventive Services for Hereditary Breast and Ovarian Cancer in the Czech Republic
por: Foretova, Lenka, et al.
Publicado: (2006)

ALS-N: a candidate for a next-generation synchrotron light source
por: Jackson, A, et al.
Publicado: (1998)

Preparedness for the next wave of COVID-19 in the Republic of Korea
por: Lee, Jong-Koo
Publicado: (2022)

Association of common candidate variants with vascular malformations and intracranial hemorrhage in hereditary hemorrhagic telangiectasia
por: Pawlikowska, Ludmila, et al.
Publicado: (2018)

Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia–Alania
por: Petrova, Nika, et al.
Publicado: (2023)

Candidate Modifier Genes for the Penetrance of Leber’s Hereditary Optic Neuropathy
por: Cheng, Hui-Chen, et al.
Publicado: (2022)

1201. Sarcoidosis Candidate Microbes Identified by Next Generation Sequencing
por: Kriesel, John D, et al.
Publicado: (2020)

The Genetic Basis of the Hereditary Ataxias
por: Critchley, E. M. R.
Publicado: (1969)

Hereditary Thrombophilia and thrombotic events in pregnancy: single-center experience
por: Coriu, L, et al.
Publicado: (2014)

Hereditary Cancer Risk Assessment: Challenges for the Next-Gen Sequencing Era
por: Pinheiro, Hugo, et al.
Publicado: (2015)

Targeted Next Generation Sequencing (NGS) to Diagnose Hereditary Hemolytic Anemias
por: Bharadwaj, Rishab, et al.
Publicado: (2020)

Hereditary prostate cancer in African American families: linkage analysis using markers that map to five candidate susceptibility loci
por: Brown, W M, et al.
Publicado: (2004)

Oscillospira - a candidate for the next-generation probiotics
por: Yang, Jingpeng, et al.
Publicado: (2021)

Could nucleocapsid be a next-generation COVID-19 vaccine candidate – author's reply
por: Oronsky, Bryan, et al.
Publicado: (2022)

Lynch Syndrome Germline Mutations in Breast Cancer: Next Generation Sequencing Case-Control Study of 1,263 Participants
por: Nikitin, Aleksey G., et al.
Publicado: (2020)

Design and validation of a next generation sequencing assay for hereditary BRCA1 and BRCA2 mutation testing
por: Kang, Hyunseok P., et al.
Publicado: (2016)

Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study
por: D'Amore, Angelica, et al.
Publicado: (2018)

High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic
por: Vasickova, Petra, et al.
Publicado: (2007)

Detecting genetic variations in hereditary retinal dystrophies with next-generation sequencing technology
por: Jin, Xin, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_kunqv40pfvjab16k0oi1mpv3a4