Identification of Novel Proteins Co-Purifying with Cockayne Syndrome Group B (CSB) Reveals Potential Roles for CSB in RNA Metabolism and Chromatin Dynamics.

CSB ablation induced apoptosis is mediated by increased endoplasmic reticulum stress response. PLoS One (2017) 0.75

Cell-type specific role of the RNA-binding protein, NONO, in the DNA double-strand break response in the mouse testes. DNA Repair (Amst) (2017) 0.75

A generic protein purification method for protein complex characterization and proteome exploration. Nat Biotechnol (1999) 25.13

An early haematopoietic defect in mice lacking the transcription factor GATA-2. Nature (1994) 8.60

RNA and disease. Cell (2009) 7.98

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes. Cell (1992) 4.80

Clinical application of exome sequencing in undiagnosed genetic conditions. J Med Genet (2012) 3.33

Regulation of dendritic development by neuron-specific chromatin remodeling complexes. Neuron (2007) 2.89

Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo. Mol Cell (2006) 2.84

The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH. Cell (1995) 2.78

DNA helicases: enzymes with essential roles in all aspects of DNA metabolism. Bioessays (1994) 2.65

The in vivo kinetics of RNA polymerase II elongation during co-transcriptional splicing. PLoS Biol (2011) 2.58

Laser microsurgery provides evidence for merotelic kinetochore attachments in fission yeast cells lacking Pcs1 or Clr4. Cell Cycle (2010) 2.48

ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor. Mol Cell Biol (2000) 2.34

Cockayne syndrome group B protein enhances elongation by RNA polymerase II. Proc Natl Acad Sci U S A (1997) 2.16

Identification of mutations in CUL7 in 3-M syndrome. Nat Genet (2005) 2.10

Activation of RNA polymerase I transcription by cockayne syndrome group B protein and histone methyltransferase G9a. Mol Cell (2007) 1.96

CSB is a component of RNA pol I transcription. Mol Cell (2002) 1.93

Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome. Mol Cell (2005) 1.89

Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes. Mol Cell Biol (1997) 1.83

A ubiquitin-binding domain in Cockayne syndrome B required for transcription-coupled nucleotide excision repair. Mol Cell (2010) 1.79

Reduced RNA polymerase II transcription in intact and permeabilized Cockayne syndrome group B cells. Proc Natl Acad Sci U S A (1997) 1.74

Cockayne syndrome group B protein (CSB) plays a general role in chromatin maintenance and remodeling. Proc Natl Acad Sci U S A (2006) 1.64

When transcription and repair meet: a complex system. Trends Genet (2006) 1.62

Unwinding chromatin for development and growth: a few genes at a time. Trends Genet (2007) 1.57

Involvement of Matrin 3 and SFPQ/NONO in the DNA damage response. Cell Cycle (2010) 1.48

Activation of p53 or loss of the Cockayne syndrome group B repair protein causes metaphase fragility of human U1, U2, and 5S genes. Mol Cell (2000) 1.46

Cockayne syndrome group B cellular and biochemical functions. Am J Hum Genet (2003) 1.46

Identification of the polypyrimidine tract binding protein-associated splicing factor.p54(nrb) complex as a candidate DNA double-strand break rejoining factor. J Biol Chem (2004) 1.46

High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44. Hum Genet (2011) 1.43

The sensitivity of Cockayne's syndrome cells to DNA-damaging agents is not due to defective transcription-coupled repair of active genes. Mol Cell Biol (1996) 1.41

Cockayne syndrome: defective repair of transcription? EMBO J (1997) 1.40

Neuropathology of Cockayne syndrome: Evidence for impaired development, premature aging, and neurodegeneration. Mech Ageing Dev (2009) 1.37

Casein kinase 1 is required for efficient removal of Rec8 during meiosis I. Cell Cycle (2010) 1.36

Efficient immortalization and morphological transformation of human fibroblasts by transfection with SV40 DNA linked to a dominant marker. Exp Cell Res (1986) 1.35

Cockayne syndrome B protein regulates the transcriptional program after UV irradiation. EMBO J (2006) 1.34

Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage? DNA Repair (Amst) (2008) 1.25

Multiple roles of class I HDACs in proliferation, differentiation, and development. Cell Mol Life Sci (2012) 1.22

Increased apoptosis, p53 up-regulation, and cerebellar neuronal degeneration in repair-deficient Cockayne syndrome mice. Proc Natl Acad Sci U S A (2007) 1.15

Tandem affinity purification of functional TAP-tagged proteins from human cells. Nat Protoc (2007) 1.15

CSB protein is (a direct target of HIF-1 and) a critical mediator of the hypoxic response. EMBO J (2008) 1.13

New insights for understanding the transcription-coupled repair pathway. DNA Repair (Amst) (2006) 1.12

A role for DEAD box 1 at DNA double-strand breaks. Mol Cell Biol (2008) 1.10

The central role of chromatin maintenance in aging. Aging (Albany NY) (2009) 1.07

PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa. Hum Mol Genet (2011) 1.04

PSF/p54(nrb) stimulates "jumping" of DNA topoisomerase I between separate DNA helices. Biochemistry (2000) 1.01

Cockayne syndrome B protein (CSB): linking p53, HIF-1 and p300 to robustness, lifespan, cancer and cell fate decisions. Cell Cycle (2009) 0.99

CSA and CSB proteins interact with p53 and regulate its Mdm2-dependent ubiquitination. Cell Cycle (2011) 0.96

Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I-DNA covalent complex. Genes Cells (2010) 0.90

An improved strategy for tandem affinity purification-tagging of Schizosaccharomyces pombe genes. Proteomics (2009) 0.90

Interaction between the Cockayne syndrome B and p53 proteins: implications for aging. Aging (Albany NY) (2012) 0.89

Is malfunction of the ubiquitin proteasome system the primary cause of alpha-synucleinopathies and other chronic human neurodegenerative disease? Biochim Biophys Acta (2008) 0.88

Control of alternative pre-mRNA splicing by RNA Pol II elongation: faster is not always better. IUBMB Life (2003) 0.88

Does interference between replication and transcription contribute to genomic instability in cancer cells? Cell Cycle (2010) 0.85

Identification of phytochrome-interacting protein candidates in Arabidopsis thaliana by co-immunoprecipitation coupled with MALDI-TOF MS. Proteomics (2006) 0.84

The cockayne syndrome B protein is essential for neuronal differentiation and neuritogenesis. Cell Death Dis (2014) 0.83

Ku86 modulates DNA topoisomerase I-mediated radiosensitization, but not cytotoxicity, in mammalian cells. Cancer Res (2005) 0.81

The CSB repair factor is overexpressed in cancer cells, increases apoptotic resistance, and promotes tumor growth. DNA Repair (Amst) (2013) 0.80

Functional proteomics. Clin Chim Acta (2005) 0.78

Interaction between the Cockayne syndrome B and p53 proteins: implications for aging. Aging (Albany NY) (2012) 0.89