Cargando…

Missense and Nonsense Mutations of P53 Gene in Patients with Colorectal Adenocarcinoma in Isfahan, Central Iran

Detalles Bibliográficos
Autores principales:	Golmohammadi, R, Namazi, M J, Nikbakht, M, Salehi, M
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Kowsar 2011
Materias:	Letter to Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371946/ https://www.ncbi.nlm.nih.gov/pubmed/22737468

Ejemplares similares

Characterization and Prognostic Value of Mutations in Exons 5 and 6 of the p53 Gene in Patients with Colorectal Cancers in Central Iran
por: Golmohammadi, Rahim, et al.
Publicado: (2013)

Indoor Radon Levels in Selected Houses in Isfahan, Central Iran
por: REZAEE EBRAHIM SARAEE, Khadijeh, et al.
Publicado: (2014)

Accidents in Children Under 5 Years in Isfahan, Iran
por: Lak, Rohollah, et al.
Publicado: (2014)

Dermatophytes contamination of wrestling mats in sport centers of Isfahan, Iran
por: Shadzi, Shahla, et al.
Publicado: (2014)

Comment on “Prevalence of Occult Hepatitis B Virus Infection in Hemodialysis Patients in Isfahan, Iran”
por: Li Cavoli, Gioacchino, et al.
Publicado: (2017)

Hereditary nonpolyposis colorectal cancer and familial colorectal cancer in Central part of Iran, Isfahan
por: Nemati, Amin, et al.
Publicado: (2012)

A survey on herpes simplex type 2 antibody among pregnant women in Isfahan, Iran
por: Shahraki, Azar Danesh, et al.
Publicado: (2010)

Surveillance on the 2009 pandemic influenza A (H1N1) virus, Isfahan, Iran
por: Babak, Anahita, et al.
Publicado: (2011)

High Prevalence of Rare Mutations in the Beta Globin Gene in an Ethnic Group in Iran
por: Galehdari, H, et al.
Publicado: (2011)

Level of knowledge of dental practitioners in Isfahan, Iran about cone-beam computed tomography and digital radiography
por: Mehdizadeh, Mojdeh, et al.
Publicado: (2015)

Immunodeficiency and disseminated mycobacterial infection associated with homozygous nonsense mutation of IKKβ()
por: Burns, Siobhan O., et al.
Publicado: (2014)

Nonsense and missense mutation of mitochondrial ND6 gene promotes cell migration and invasion in human lung adenocarcinoma
por: Yuan, Yang, et al.
Publicado: (2015)

Gene characteristics predicting missense, nonsense and frameshift mutations in tumor samples
por: Gorlov, Ivan P., et al.
Publicado: (2018)

The emergence of multidrug-resistant clone ST664 Pseudomonas aeruginosa in a referral burn hospital, Isfahan, Iran
por: Vaez, Hamid, et al.
Publicado: (2017)

Genetic Identification of Echinococcus granulosus Isolates from Domestic Animals in Sabzevar, Northeast Iran
por: ELYASI, Hossein, et al.
Publicado: (2020)

KRAS, KIT and TP53 mutations in mother’s and daughter’s gastric cardia adenocarcinomas
por: Gluszek, Stanislaw, et al.
Publicado: (2018)

A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP
por: Çağlayan, Ahmet Okay, et al.
Publicado: (2016)

Association of TP53 gene codon 72 polymorphism with endometriosis risk in Isfahan
por: Nikbakht Dastjerdi, Mehdi, et al.
Publicado: (2013)

Case study of a patient with cryptozoospermia associated with a recessive TEX15 nonsense mutation
por: Wang, Xiong, et al.
Publicado: (2018)

Hepatitis G virus exposure in dialysis patients and blood donors in Isfahan-Iran
por: Salehi, Maryam, et al.
Publicado: (2014)

FATP4 missense and nonsense mutations cause similar features in Ichthyosis Prematurity Syndrome
por: Sobol, Maria, et al.
Publicado: (2011)

A Novel Missense Mutation in BRAF Caused Cardio-Facio-Cutaneous Syndrome
por: Hazan, Filiz, et al.
Publicado: (2013)

Costs and outcomes of colorectal cancer screening program in Isfahan, Iran
por: Rahimi, Farimah, et al.
Publicado: (2023)

Is prostatic adenocarcinoma in a relationship with Human Papilloma Virus in Isfahan -Iran
por: Mokhtari, Mojgan, et al.
Publicado: (2013)

Retinal detachment in Isfahan Feiz hospital (an epidemiologic study)
por: Kianersi, Farzan, et al.
Publicado: (2009)

Correlation of inflammatory and nutritional indexes in Isfahan hemodialysis patients
por: Kafeshani, Omolbanin, et al.
Publicado: (2010)

A missense TCF1 mutation in a patient with mody‐3 and liver adenomatosis
por: Lerario, Antonio Marcondes, et al.
Publicado: (2010)

X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase
por: Agrebi, Nourhen, et al.
Publicado: (2021)

Panel testing reveals nonsense and missense CDH1 mutations in families without hereditary diffuse gastric cancer
por: Huynh, Julie M., et al.
Publicado: (2016)

Association of Pathogenic Missense and Nonsense Mutations in Mitochondrial COII Gene with Familial Adenomatous Polyposis (FAP)
por: Shaker Ardakani, Zahra, et al.
Publicado: (2020)

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Case Report of a Novel Nonsense Mutation in the SACS Gene
por: Agarwal, Ayush, et al.
Publicado: (2020)

Geographical Distribution of Scorpion Odontobuthus doriae in Isfahan Province, Central Iran
por: Dehghani, Rouhullah, et al.
Publicado: (2017)

cDNA sequencing improves the detection of P53 missense mutations in colorectal cancer
por: Szybka, Malgorzata, et al.
Publicado: (2009)

Temporal Trends of Incidence of Colorectal Cancer in Isfahan, Iran, 2000–2011
por: Rejali, Mehri, et al.
Publicado: (2018)

A Novel Missense Mutation of Keratin 17 Gene in a Chinese Family with Steatocystoma Multiplex
por: Ha, Wei-Wei, et al.
Publicado: (2013)

Prevalence of Helicobacter pylori vacA different genotypes in Isfahan, Iran
por: Havaei, S. Asghar, et al.
Publicado: (2014)

Nosocomial infections and antimicrobial resistance pattern in a tertiary referral hospital in Hamedan, Iran
por: Ranjbar, Mitra, et al.
Publicado: (2012)

ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function
por: de Majo, Martina, et al.
Publicado: (2018)

Mice with missense and nonsense NF1 mutations display divergent phenotypes compared with human neurofibromatosis type I
por: Li, Kairong, et al.
Publicado: (2016)

A Novel Nonsense Mutation in Leucine-Rich, Glioma-Inactivated-1 Gene as the Underlying Cause of Familial Temporal Lobe Epilepsy
por: Kanwal, Sumaira, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_eviv1m86l0neku1t7fm6llc6nq