Splicing mutations in the PDHA1 gene

Splicing mutations in the PDHA1 gene

Bibliografiset tiedot
Päätekijät:	Ridout, C, Brown, R, Brown, G
Aineistotyyppi:	Journal article
Julkaistu:	2008

Samankaltaisia teoksia

A putative exonic splicing enhancer in exon 7 of the PDHA1 gene affects splicing of adjacent exons.
Tekijä: Ridout, C, et al.
Julkaistu: (2008)

Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiency
Tekijä: Ridout, C, et al.
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Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiency.
Tekijä: Ridout, C, et al.
Julkaistu: (2008)

ERN1 KNOCKDOWN AFFECTS THE EXPRESSION OF PDHA1, PDHB, PDHX, DLD, AND DLAT GENES AND MODIFIES THEIR HYPOXIC REGULATION
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RNF4 mediated degradation of PDHA1 promotes colorectal cancer metabolism and metastasis
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Comprehensive analyses of PDHA1 that serves as a predictive biomarker for immunotherapy response in cancer
Tekijä: Langmei Deng, et al.
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Clinical exome sequencing reveals a mutation in PDHA1 in Leigh syndrome: A case of a Chinese boy with lethal neuropathy
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AMPK maintains TCA cycle through sequential phosphorylation of PDHA to promote tumor metastasis
Tekijä: Zhen Cai, et al.
Julkaistu: (2020-11-01)

Artificial intelligence reveals dysregulation of osteosarcoma and cuproptosis-related biomarkers, PDHA1, CDKN2A and neutrophils
Tekijä: Jie Jiang, et al.
Julkaistu: (2023-03-01)

PDHA1 hyperacetylation-mediated lactate overproduction promotes sepsis-induced acute kidney injury via Fis1 lactylation
Tekijä: Sheng An, et al.
Julkaistu: (2023-07-01)

Multi-omics Insights into PDHA1 as a Predictive Biomarker for Prognosis, Immunotherapy Efficacy, and Drug Sensitivity in Hepatocellular Carcinoma
Tekijä: Yong Pan, et al.
Julkaistu: (2024-11-01)

SIRT3 elicited an anti‐Warburg effect through HIF1α/PDK1/PDHA1 to inhibit cholangiocarcinoma tumorigenesis
Tekijä: Lei Xu, et al.
Julkaistu: (2019-05-01)

Case Report: A novel hemizygous missense PDHA1 variant in a Vietnamese boy with pyruvate dehydrogenase E1-alpha deficiency
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Identification of immunogenic proteins and evaluation of recombinant PDHA1 and GAPDH as potential vaccine candidates against Streptococcus iniae infection in flounder (Paralichthys olivaceus).
Tekijä: Xiuzhen Sheng, et al.
Julkaistu: (2018-01-01)

Identification of aberrant splicing events in myelodysplastic syndrome patients with splicing factor gene mutations
Tekijä: Pellagatti, A, et al.
Julkaistu: (2017)

Functional analysis of splicing mutations in exon 7 of <it>NF1 </it>gene
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Hereditary cancer genes are highly susceptible to splicing mutations.
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Julkaistu: (2018-03-01)

Exosomal miR-21-5p from glioma associated mesenchymal stem cells promotes the progression and glycolysis of glioblastoma via PDHA1
Tekijä: Yanbin Zhang, et al.
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Splice site mutations in the ATP7A gene.
Tekijä: Tina Skjørringe, et al.
Julkaistu: (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
Tekijä: Vânia Gaio, et al.
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Deep learning for alternative splicing
Tekijä: Brown, R
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Functional analysis of the GPAT4 gene mutation predicted to affect splicing
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Splicing factor mutations in the myelodysplastic syndromes: target genes and therapeutic approaches
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Alternative Splicing of Barley Clock Genes in Response to Low Temperature.
Tekijä: Cristiane P G Calixto, et al.
Julkaistu: (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
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An extended nomenclature for mammalian V-ATPase subunit genes and splice variants.
Tekijä: Kevin C Miranda, et al.
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NF1 Gene Novel Splicing Mutations in a Chinese Family with Neurofibromatosis Type 1: Case Series
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Calculation of Splicing Potential from the Alternative Splicing Mutation Database
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Induced splice site mutation generates alternative intron splicing in starch synthase II (SSII) gene in rice
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Exploring the Crosstalk Between LMNA and Splicing Machinery Gene Mutations in Dilated Cardiomyopathy
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Identification of a novel splice site mutation in the SERAC1 gene responsible for the MEGDHEL syndrome
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Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in <it>MR </it>gene
Tekijä: Kaito Hiroshi, et al.
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Mutations in hnRNP A1 drive neurodegeneration and alternative RNA splicing of neuronal gene targets
Tekijä: Ansalna Ansari, et al.
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The Alternative Splicing Mutation Database: a hub for investigations of alternative splicing using mutational evidence
Tekijä: Afonin Kirill A, et al.
Julkaistu: (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>)
Tekijä: Xiuzhen Sheng, et al.
Julkaistu: (2023-03-01)

Partial rescue of truncating mutations in the ATRX gene through unusual intra-exonic splicing
Tekijä: Malik, N, et al.
Julkaistu: (2006)

Alternative Splicing of Circadian Clock Genes Correlates With Temperature in Field-Grown Sugarcane
Tekijä: Luíza L. B. Dantas, et al.
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Mutations in the gene for the E1β subunit: a novel cause of pyruvate dehydrogenase deficiency
Tekijä: Brown, R, et al.
Julkaistu: (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
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A functional alternative splicing mutation in AIRE gene causes autoimmune polyendocrine syndrome type 1.
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