Cargando…

Role of p16 deletion and Bmi1 copy number variation in glioma

Detalles Bibliográficos
Autores principales:	Chetan, GK, Sibin, M K, Bhat, Dhananjaya I, Lavanya, Ch, Jeru, Manoj M, Geethashree, N
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2014
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042331/ http://dx.doi.org/10.1186/1755-8166-7-S1-P11

Ejemplares similares

Correlation o P16 and Bmi1 gene expression in human high grade glioma
por: Sibin, M K, et al.
Publicado: (2014)

Promoter methylation of PTEN gene in high grade gliomas
por: Lavanya, C, et al.
Publicado: (2014)

Two gene polymorphisms (rs4977756 and rs11515) in CDKN2A/B and glioma risk in South Indian population
por: Sibin, M.K., et al.
Publicado: (2016)

The role of direct DNA repair gene O6-methylguanine-DNA methyltransferase (MGMT) in high grade malignant glioma
por: Manoj, M Jeru, et al.
Publicado: (2014)

Polymorphisms of apolipoprotein E and aneurysmal subarachnoid haemorrhage: A meta-analysis
por: Arati, S., et al.
Publicado: (2016)

Rare Copy Number Deletions Predict Individual Variation in Intelligence
por: Yeo, Ronald A., et al.
Publicado: (2011)

Identification of copy number variations and common deletion polymorphisms in cattle
por: Bae, Joon Seol, et al.
Publicado: (2010)

Who ever heard of 16p11.2 deletion syndrome? Parents’ perspectives on a susceptibility copy number variation syndrome
por: Kleinendorst, Lotte, et al.
Publicado: (2020)

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome
por: Bassett, Anne S., et al.
Publicado: (2008)

DPYD Exon 4 Deletion Associated with Fluoropyrimidine Toxicity and Importance of Copy Number Variation
por: Wigle, Theodore J., et al.
Publicado: (2023)

Comparing copy-number profiles under multi-copy amplifications and deletions
por: Cordonnier, Garance, et al.
Publicado: (2020)

Copy number variations and cancer
por: Shlien, Adam, et al.
Publicado: (2009)

Copy number variations and stroke
por: Colaianni, Valeria, et al.
Publicado: (2016)

Copy Number Variations and Schizophrenia
por: Szecówka, Kamila, et al.
Publicado: (2022)

Copy Number Variation and Osteoporosis
por: Lovšin, Nika
Publicado: (2023)

Deletions of CDKN2A and MTAP Detected by Copy-Number Variation Array Are Associated with Loss of p16 and MTAP Protein in Pleural Mesothelioma
por: Vrugt, Bart, et al.
Publicado: (2023)

Genomic copy number variation correlates with survival outcomes in WHO grade IV glioma
por: Buchwald, Zachary S., et al.
Publicado: (2020)

Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development
por: Qiu, Yuqi, et al.
Publicado: (2019)

Copy Number Variations Due to Large Genomic Deletion in X-Linked Chronic Granulomatous Disease
por: Arai, Takashi, et al.
Publicado: (2012)

Deleted copy number variation of Hanwoo and Holstein using next generation sequencing at the population level
por: Shin, Dong-Hyun, et al.
Publicado: (2014)

Gene expression patterns of chicken neuregulin 3 in association with copy number variation and frameshift deletion
por: Abe, Hideaki, et al.
Publicado: (2017)

Copy number variation in bipolar disorder
por: Green, E K, et al.
Publicado: (2016)

Copy-number-variation and copy-number-alteration region detection by cumulative plots
por: Li, Wentian, et al.
Publicado: (2009)

Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing
por: Bai, Wei, et al.
Publicado: (2023)

Insertion-deletions burden in copy number polymorphisms of the Tibetan population
por: Veerappa, Avinash M., et al.
Publicado: (2014)

Identification of Dysregulated Competitive Endogenous RNA Networks Driven by Copy Number Variations in Malignant Gliomas
por: Xu, Jinyuan, et al.
Publicado: (2019)

Systematic analysis of enhancer regulatory circuit perturbation driven by copy number variations in malignant glioma
por: Xiao, Jun, et al.
Publicado: (2021)

New Copy Number Variations in Schizophrenia
por: Magri, Chiara, et al.
Publicado: (2010)

Copy number variation in African Americans
por: McElroy, Joseph P, et al.
Publicado: (2009)

Copy number variation goes clinical
por: Le Caignec, Cédric, et al.
Publicado: (2009)

Copy number variation in Parkinson's disease
por: Toft, Mathias, et al.
Publicado: (2010)

Copy number variation in the bovine genome
por: Fadista, João, et al.
Publicado: (2010)

Copy Number Variation in Thai Population
por: Suktitipat, Bhoom, et al.
Publicado: (2014)

Copy Number Variation in the Horse Genome
por: Ghosh, Sharmila, et al.
Publicado: (2014)

Copy number variations among silkworms
por: Zhao, Qian, et al.
Publicado: (2014)

Copy number variation and neuropsychiatric illness
por: Rees, Elliott, et al.
Publicado: (2021)

Copy Number Variations in Neuropsychiatric Disorders
por: Büki, Gergely, et al.
Publicado: (2023)

Plasmodium copy number variation scan: gene copy numbers evaluation in haploid genomes
por: Beghain, Johann, et al.
Publicado: (2016)

Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi Arabia
por: Naseer, Muhammad Imran, et al.
Publicado: (2015)

Genomic characteristics of cattle copy number variations
por: Hou, Yali, et al.
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_i1g4a9fcgj9ooc1u6vm8hoc540