Splicing mutations in the PDHA1 gene

Splicing mutations in the PDHA1 gene

Bibliografski detalji
Glavni autori:	Ridout, C, Brown, R, Brown, G
Format:	Journal article
Izdano:	2008

Slični predmeti

A putative exonic splicing enhancer in exon 7 of the PDHA1 gene affects splicing of adjacent exons.
od: Ridout, C, i dr.
Izdano: (2008)

Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiency
od: Ridout, C, i dr.
Izdano: (2008)

Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiency.
od: Ridout, C, i dr.
Izdano: (2008)

ERN1 KNOCKDOWN AFFECTS THE EXPRESSION OF PDHA1, PDHB, PDHX, DLD, AND DLAT GENES AND MODIFIES THEIR HYPOXIC REGULATION
od: Y.P. KHIKHLO, i dr.
Izdano: (2024-04-01)

RNF4 mediated degradation of PDHA1 promotes colorectal cancer metabolism and metastasis
od: Jierong Chen, i dr.
Izdano: (2024-11-01)

Comprehensive analyses of PDHA1 that serves as a predictive biomarker for immunotherapy response in cancer
od: Langmei Deng, i dr.
Izdano: (2022-08-01)

Clinical exome sequencing reveals a mutation in PDHA1 in Leigh syndrome: A case of a Chinese boy with lethal neuropathy
od: Ke Gong, i dr.
Izdano: (2021-04-01)

AMPK maintains TCA cycle through sequential phosphorylation of PDHA to promote tumor metastasis
od: Zhen Cai, i dr.
Izdano: (2020-11-01)

Artificial intelligence reveals dysregulation of osteosarcoma and cuproptosis-related biomarkers, PDHA1, CDKN2A and neutrophils
od: Jie Jiang, i dr.
Izdano: (2023-03-01)

PDHA1 hyperacetylation-mediated lactate overproduction promotes sepsis-induced acute kidney injury via Fis1 lactylation
od: Sheng An, i dr.
Izdano: (2023-07-01)

Multi-omics Insights into PDHA1 as a Predictive Biomarker for Prognosis, Immunotherapy Efficacy, and Drug Sensitivity in Hepatocellular Carcinoma
od: Yong Pan, i dr.
Izdano: (2024-11-01)

SIRT3 elicited an anti‐Warburg effect through HIF1α/PDK1/PDHA1 to inhibit cholangiocarcinoma tumorigenesis
od: Lei Xu, i dr.
Izdano: (2019-05-01)

Case Report: A novel hemizygous missense PDHA1 variant in a Vietnamese boy with pyruvate dehydrogenase E1-alpha deficiency
od: Thi Thanh Ngan Nguyen, i dr.
Izdano: (2024-12-01)

Identification of immunogenic proteins and evaluation of recombinant PDHA1 and GAPDH as potential vaccine candidates against Streptococcus iniae infection in flounder (Paralichthys olivaceus).
od: Xiuzhen Sheng, i dr.
Izdano: (2018-01-01)

Identification of aberrant splicing events in myelodysplastic syndrome patients with splicing factor gene mutations
od: Pellagatti, A, i dr.
Izdano: (2017)

Functional analysis of splicing mutations in exon 7 of <it>NF1 </it>gene
od: Calvieri Stefano, i dr.
Izdano: (2007-02-01)

Hereditary cancer genes are highly susceptible to splicing mutations.
od: Christy L Rhine, i dr.
Izdano: (2018-03-01)

Exosomal miR-21-5p from glioma associated mesenchymal stem cells promotes the progression and glycolysis of glioblastoma via PDHA1
od: Yanbin Zhang, i dr.
Izdano: (2025-01-01)

Splice site mutations in the ATP7A gene.
od: Tina Skjørringe, i dr.
Izdano: (2011-04-01)

codY and pdhA Expression Is Induced in Staphylococcus epidermidis Biofilm and Planktonic Populations With Higher Proportions of Viable but Non-Culturable Cells
od: Vânia Gaio, i dr.
Izdano: (2021-11-01)

Deep learning for alternative splicing
od: Brown, R
Izdano: (2019)

Functional analysis of the GPAT4 gene mutation predicted to affect splicing
od: Sergey A. Bursakov, i dr.
Izdano: (2024-12-01)

Splicing factor mutations in the myelodysplastic syndromes: target genes and therapeutic approaches
od: Armstrong, R, i dr.
Izdano: (2017)

Alternative Splicing of Barley Clock Genes in Response to Low Temperature.
od: Cristiane P G Calixto, i dr.
Izdano: (2016-01-01)

Adaptive mutation in influenza A virus non-structural gene is linked to host switching and induces a novel protein by alternative splicing
od: Mohammed Selman, i dr.
Izdano: (2012-07-01)

An extended nomenclature for mammalian V-ATPase subunit genes and splice variants.
od: Kevin C Miranda, i dr.
Izdano: (2010-03-01)

NF1 Gene Novel Splicing Mutations in a Chinese Family with Neurofibromatosis Type 1: Case Series
od: Wu T, i dr.
Izdano: (2022-10-01)

Calculation of Splicing Potential from the Alternative Splicing Mutation Database
od: Afonin Kirill A, i dr.
Izdano: (2008-02-01)

Induced splice site mutation generates alternative intron splicing in starch synthase II (SSII) gene in rice
od: Chao Chen, i dr.
Izdano: (2017-11-01)

Exploring the Crosstalk Between LMNA and Splicing Machinery Gene Mutations in Dilated Cardiomyopathy
od: Hind C. Zahr, i dr.
Izdano: (2018-07-01)

Identification of a novel splice site mutation in the SERAC1 gene responsible for the MEGDHEL syndrome
od: Sarah Snanoudj, i dr.
Izdano: (2019-08-01)

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in <it>MR </it>gene
od: Kaito Hiroshi, i dr.
Izdano: (2009-11-01)

Mutations in hnRNP A1 drive neurodegeneration and alternative RNA splicing of neuronal gene targets
od: Ansalna Ansari, i dr.
Izdano: (2025-03-01)

The Alternative Splicing Mutation Database: a hub for investigations of alternative splicing using mutational evidence
od: Afonin Kirill A, i dr.
Izdano: (2008-02-01)

Development and Evaluation of Recombinant B-Cell Multi-Epitopes of PDHA1 and GAPDH as Subunit Vaccines against <i>Streptococcus iniae</i> Infection in Flounder (<i>Paralichthys olivaceus</i>)
od: Xiuzhen Sheng, i dr.
Izdano: (2023-03-01)

Partial rescue of truncating mutations in the ATRX gene through unusual intra-exonic splicing
od: Malik, N, i dr.
Izdano: (2006)

Alternative Splicing of Circadian Clock Genes Correlates With Temperature in Field-Grown Sugarcane
od: Luíza L. B. Dantas, i dr.
Izdano: (2019-12-01)

Mutations in the gene for the E1β subunit: a novel cause of pyruvate dehydrogenase deficiency
od: Brown, R, i dr.
Izdano: (2004)

Correction: When is a mutation not a mutation: the case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in trans
od: Michelle Wong-Brown, i dr.
Izdano: (2022-05-01)

A functional alternative splicing mutation in AIRE gene causes autoimmune polyendocrine syndrome type 1.
od: Junyu Zhang, i dr.
Izdano: (2013-01-01)