Cargando…

Effect of the novel Moroccan BRCA1 and BRCA2 frameshift mutations

Detalles Bibliográficos
Autores principales:	Tazzite, Amal, Jouhadi, Hassan, Hamzi, Khalil, Benider, Abdellatif, Nadifi, Sellama
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2013
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3758742/ https://www.ncbi.nlm.nih.gov/pubmed/24019637 http://dx.doi.org/10.4103/0971-6866.116114

Ejemplares similares

Clinical and pathological features of BRCA1/2 tumors in a sample of high-risk Moroccan breast cancer patients
por: Jouhadi, Hassan, et al.
Publicado: (2016)

Relationship Between Family History of Breast Cancer and Clinicopathological Features in Moroccan Patients
por: Tazzite, Amal, et al.
Publicado: (2013)

Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients
por: El Khachibi, Meryam, et al.
Publicado: (2015)

Association between ABCB1 C3435T polymorphism and breast cancer risk: a Moroccan case-control study and meta-analysis
por: Tazzite, Amal, et al.
Publicado: (2016)

The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population
por: Marouf, Chaymaa, et al.
Publicado: (2015)

Large scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,297 individuals
por: Hamzi, Khalil, et al.
Publicado: (2013)

Next-generation sequencing of BRCA1 and BRCA2 genes in Moroccan prostate cancer patients with positive family history
por: Salmi, Fatiha, et al.
Publicado: (2021)

Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals
por: Hamzi, Khalil, et al.
Publicado: (2011)

Duchenne muscular dystrophy: Advances in molecular appraoch
por: Benitto, Afaf, et al.
Publicado: (2013)

Comparison of Targeted Next-Generation and Sanger Sequencing for the BRCA1 and BRCA2 Mutation Screening
por: Park, Joonhong, et al.
Publicado: (2016)

Comment on ‘The incidence of leukaemia in women with BRCA1 and BRCA2 mutations: an International Prospective Cohort Study'
por: Friedenson, Bernard
Publicado: (2016)

Comment on ‘The incidence of leukaemia in women with BRCA1 and BRCA2 mutations: an International Prospective Cohort Study'
por: Paradiso, A V, et al.
Publicado: (2016)

Response to ‘Comments on 'The incidence of leukaemia in women with BRCA1 and BRCA2 mutations: an International Prospective Cohort Study''
por: Narod, Steven A
Publicado: (2016)

Novel BRCA1 and BRCA2 genomic rearrangements in Southern Chinese breast/ovarian cancer patients
por: Kwong, Ava, et al.
Publicado: (2012)

A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report
por: Karkar, Adnane, et al.
Publicado: (2015)

Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?
por: Hamzi, Khalil, et al.
Publicado: (2010)

BRCA2 Reversion Mutation Identified by Liquid Biopsy After Durable Response to FOLFIRINOX in BRCA2-Associated Pancreatic Cancer
por: Kondo, Tomohiro, et al.
Publicado: (2020)

Analysis of PTEN in two BRCA1 and BRCA2 wild-type familial breast cancer patients
por: Akouchekian, Mansoureh, et al.
Publicado: (2015)

Genetics of Glioblastoma in Moroccan population: Review of literature
por: Idrissi, Hossam Hilal El, et al.
Publicado: (2018)

BRCA1 c.4987-3C>G is a pathogenic mutation
por: Brandão, Rita D., et al.
Publicado: (2011)

Prevalence and reclassification of BRCA1 and BRCA2 variants in a large, unselected Chinese Han breast cancer cohort
por: Liu, Yun, et al.
Publicado: (2021)

IL23R and ATG16L1 variants in Moroccan patients with inflammatory bowel disease
por: Serbati, Nadia, et al.
Publicado: (2014)

BRCA1 polymorphisms.
por: Campbell, I. G., et al.
Publicado: (1997)

Reduced DNA repair in BRCA1 mutation carriers undetectable before onset of breast cancer?
por: Vogel, W, et al.
Publicado: (2007)

MTHFR C677T polymorphism and risk of nonsyndromic cleft lip with or without cleft palate in the Moroccan population
por: Rafik, Amine, et al.
Publicado: (2019)

The Moroccan human mutation database
por: Ratbi, Ilham, et al.
Publicado: (2008)

Molecular Trajectory of BRCA1 and BRCA2 Mutations
por: Hatano, Yuichiro, et al.
Publicado: (2020)

Mutation Screening of the BRCA1 Gene in Early Onset and Familial Breast/Ovarian Cancer in Moroccan Population
por: Laraqui, Abdelilah, et al.
Publicado: (2012)

Incorporating tumor immunohistochemical markers in BRCA1 and BRCA2 carrier prediction
por: Tai, Yu Chuan, et al.
Publicado: (2008)

Reply: Reduced DNA repair in BRCA1 mutation carriers undetectable before onset of breast cancer?
por: Narod, S A
Publicado: (2007)

BRCA1 frameshift variants leading to extended incorrect protein C termini
por: Nepomuceno, Thales C., et al.
Publicado: (2023)

Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile
por: Kindil, Zineb, et al.
Publicado: (2017)

Analysis of BRCA1- and BRCA2-Related Pancreatic Cancer and Survival
por: Boursi, Ben, et al.
Publicado: (2023)

BRCA1 and BRCA2 mutations in Scotland and Northern Ireland
Publicado: (2003)

The germline mutational landscape of BRCA1 and BRCA2 in Brazil
por: Palmero, Edenir Inêz, et al.
Publicado: (2018)

Prediction of carrying a BRCA1 or BRCA2 mutation
por: Lee, Kyung-Hun
Publicado: (2023)

Association of Multidrug Resistance Gene-1 (MDR1 C1236T) Polymorphism with the Risk of Acute Myeloid Leukemia in a Moroccan Population
por: Boujmia, Oum Kaltoum Ait, et al.
Publicado: (2020)

Germline mutations in 5’ to c.7914 of BRCA2 significantly increase risk of prostate cancer
por: Ruan, Xiao-Hao, et al.
Publicado: (2022)

Germline BRCA1/BRCA2 mutations among high risk breast cancer patients in Jordan
por: Abdel-Razeq, Hikmat, et al.
Publicado: (2018)

Predominance of BRCA2 Mutation and Estrogen Receptor Positivity in Unselected Breast Cancer with BRCA1 or BRCA2 Mutation
por: Pujol, Pascal, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_q4r7aj48rp1ov1l4h4i76i83rk