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IFRD1 gene

Known as: TETRADECANOYL PHORBOL ACETATE-INDUCED SEQUENCE 7, interferon related developmental regulator 1, TPA-INDUCED SEQUENCE 7 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Identification of IFRD1 variant in a Han Chinese family with autosomal dominant hereditary spastic paraplegia associated with peripheral neuropathy and ataxia
Spinocerebellar ataxias (SCAs) are a group of autosomal dominant, clinically heterogeneous neurodegenerative disorders. SCA18 is… Expand
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2017
2017
The transcriptional modulator Ifrd1 is a negative regulator of BMP-2-dependent osteoblastogenesis.
We previously demonstrated that the transcriptional coactivator/repressor interferon-related developmental regulator 1 (Ifrd1… Expand
2016
2016
TIS7 induces transcriptional cascade of methylosome components required for muscle differentiation
BackgroundTPA Induced Sequence 7 acts as a transcriptional co-regulator controlling the expression of genes involved in… Expand
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2016
2016
Expression and regulation of the differentiation regulators ERBB Receptor Feedback Inhibitor 1 (ERRFI1) and Interferon‐related Developmental Regulator 1 (IFRD1) during the periovulatory period in the…
The current study investigated the regulation and the spatiotemporal expression pattern of Errfi1 and Ifrd1, genex encoding… Expand
2014
2014
IFRD1 polymorphisms and gastric cancer risk in a Chinese population
The association between gene polymorphisms of IFRD1 and gastric cancer is not clear. The aim of this study was to investigate the… Expand
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2010
2010
Proprotein convertase inhibitory activities of flavonoids isolated from Oroxylum indicum.
BACKGROUND Proprotein Convertases (PCs) or Proprotein Convertase Subtilisin/Kexins (PCSKs) belong to a family of calcium… Expand
Highly Cited
2009
Highly Cited
2009
Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease
Lung disease is the major cause of morbidity and mortality in cystic fibrosis, an autosomal recessive disease caused by mutations… Expand
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2009
2009
IFRD1 polymorphisms in cystic fibrosis with potential link to altered neutrophil function
Lung disease is the major cause of morbidity and mortality in cystic fibrosis (CF), an autosomal recessive disease caused by… Expand
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1998
1998
Cloning of the human interferon-related developmental regulator (IFRD1) gene coding for the PC4 protein, a member of a novel family of developmentally regulated genes.
The rat PC4 gene had been initially isolated as a nerve growth factor-inducible sequence in PC12 cells. Although its function… Expand
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1993
1993
Expression of immediate early genes after treatment of human astrocytoma cells with radiation and taxol.
PURPOSE The promising chemotherapeutic agent, taxol, has been shown to sensitize the G18 line of human astrocytoma cells to… Expand
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