Cargando…

Cloning and characterization of a novel alternatively spliced transcript of the human CHD7 putative helicase

BACKGROUND: The CHD7 (Chromodomain Helicase DNA binding protein 7) gene encodes a member of the chromodomain family of ATP-dependent chromatin remodeling enzymes. Mutations in the CHD7 gene are found in individuals with CHARGE, a syndrome characterized by multiple birth malformations in several tiss...

Descripción completa

Detalles Bibliográficos
Autores principales:	Colin, Christian, Tobaruella, Flávia S, Correa, Ricardo G, Sogayar, Mari C, Demasi, Marcos A
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2010
Materias:	Short Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966464/ https://www.ncbi.nlm.nih.gov/pubmed/20925924 http://dx.doi.org/10.1186/1756-0500-3-252

Ejemplares similares

CHD7 promotes glioblastoma cell motility and invasiveness through transcriptional modulation of an invasion signature
por: Machado, Raquel A. C., et al.
Publicado: (2019)

Evidence of a synthetic lethality interaction between SETDB1 histone methyltransferase and CHD4 chromatin remodeling protein in a triple negative breast cancer cell line
por: Moraes-Almeida, M.S., et al.
Publicado: (2023)

AS-EAST: a functional annotation tool for putative proteins encoded by alternatively spliced transcripts
por: Shionyu, Masafumi, et al.
Publicado: (2012)

CHARGE syndrome‐associated proteins FAM172A and CHD7 influence male sex determination and differentiation through transcriptional and alternative splicing mechanisms
por: Bélanger, Catherine, et al.
Publicado: (2022)

Modulatory role of RNA helicases in MBNL-dependent alternative splicing regulation
por: Taylor, Katarzyna, et al.
Publicado: (2023)

Genetic Variability of the Functional Domains of Chromodomains Helicase DNA-Binding (CHD) Proteins
por: Cardoso, Ana R., et al.
Publicado: (2021)

Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes
por: Ng, David, et al.
Publicado: (2008)

Cloning and characterization of the mouse Mcoln1 gene reveals an alternatively spliced transcript not seen in humans
por: Falardeau, John L, et al.
Publicado: (2002)

Alternative Spliced Transcripts as Cancer Markers
por: Caballero, Otavia L., et al.
Publicado: (2001)

Role of Chromodomain-Helicase-DNA-Binding Protein 4 (CHD4) in Breast Cancer
por: Novillo, Apolonia, et al.
Publicado: (2021)

CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing
por: Kerschbamer, Emanuela, et al.
Publicado: (2022)

Alternative splicing of helicase-like transcription factor (Hltf): Intron retention-dependent activation of immune tolerance at the feto-maternal interface
por: Kaur, Gurvinder, et al.
Publicado: (2018)

The Ski2-family helicase Obelus regulates Crumbs alternative splicing and cell polarity
por: Vichas, Athea, et al.
Publicado: (2015)

Relationships between putative G-quadruplex-forming sequences, RecQ helicases, and transcription
por: Smestad, John A., et al.
Publicado: (2015)

Isolation and characterization of novel RECK tumor suppressor gene splice variants
por: Trombetta-Lima, Marina, et al.
Publicado: (2015)

Determining the impact of alternative splicing events on transcriptome dynamics
por: Wilhelm, Emmanuelle, et al.
Publicado: (2008)

Mapping splice QTLs reveals distinct transcriptional and post-transcriptional regulatory variation of gene expression and identifies putative alternative splicing variation mediating complex trait variation in pigs
por: Zhang, Fei, et al.
Publicado: (2023)

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
por: Snijders Blok, Lot, et al.
Publicado: (2018)

Advances in Chromodomain Helicase DNA-Binding (CHD) Proteins Regulating Stem Cell Differentiation and Human Diseases
por: Liu, Caojie, et al.
Publicado: (2021)

Connections between Alternative Transcription and Alternative Splicing in Mammals
por: Shabalina, Svetlana A., et al.
Publicado: (2010)

Extensive Alternative Splicing of KIR Transcripts
por: Bruijnesteijn, Jesse, et al.
Publicado: (2018)

Alternative Splicing and Transcription Elongation in Plants
por: Godoy Herz, Micaela A., et al.
Publicado: (2019)

Comprehensive analysis of mutually exclusive alternative splicing in C. elegans
por: Kuroyanagi, Hidehito, et al.
Publicado: (2014)

Changes in Alternative Splicing as Pharmacodynamic Markers for Sudemycin D6
por: Thurman, Morgan, et al.
Publicado: (2017)

DDX5/p68 RNA helicase expression is essential for initiating adipogenesis
por: Ramanathan, Nardev, et al.
Publicado: (2015)

An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome
por: Ogier, Jacqueline M., et al.
Publicado: (2018)

Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of CHD8 Haploinsufficiency
por: Wade, A. Ayanna, et al.
Publicado: (2019)

The role of chromodomain helicase DNA binding protein 1 (CHD1) in promoting an invasive prostate cancer phenotype
por: Kareddula, Aparna, et al.
Publicado: (2021)

An unclassified variant of CHD7 activates a cryptic splice site in a patient with CHARGE syndrome
por: Katoh-Fukui, Yuko, et al.
Publicado: (2018)

Fine-Tuning of the Grain Size by Alternative Splicing of GS3 in Rice
por: Liu, Lei, et al.
Publicado: (2022)

Putative transcription antiterminator RfaH contributes to Erwinia amylovora virulence
por: Klee, Sara M., et al.
Publicado: (2022)

Complexity of Bidirectional Transcription and Alternative Splicing at Human RCAN3 Locus
por: Facchin, Federica, et al.
Publicado: (2011)

Alberto Kornblihtt: Coupling alternative splicing with transcription
por: Casadio, Melina
Publicado: (2017)

Roles of alternative splicing in modulating transcriptional regulation
por: Li, Jin, et al.
Publicado: (2017)

Alternative splicing: transcriptional regulatory network in agroforestry
por: Hussain, Syed Sarfaraz, et al.
Publicado: (2023)

The putative RNase P motif in the DEAD box helicase Hera is dispensable for efficient interaction with RNA and helicase activity
por: Linden, Martin H., et al.
Publicado: (2008)

Alternative Splicing Generates Different 5′ UTRs in OCT4B Variants
por: Poursani, Ensieh M., et al.
Publicado: (2017)

The chromodomain helicase CHD4 regulates ERBB2 signaling pathway and autophagy in ERBB2(+) breast cancer cells
por: D'Alesio, Carolina, et al.
Publicado: (2019)

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
por: Blok, Lot Snijders, et al.
Publicado: (2019)

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
por: Snijders Blok, Lot, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_j6pv4fqne6s4uipd35p42tupoq