CyclinD1 Down‐Regulation and Increased Apoptosis Are Common Features of Cohesinopathies
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A. Giordano | M. Mazzola | A. Selicorni | V. Massa | A. Biondi | L. Bettini | G. Cazzaniga | G. Bellipanni | F. Cotelli | A. Pistocchi | G. Fazio | A. Cereda | L. Ferrari | V. Scagliotti | C. Gaston-Massuet | Federica Graziola | Laura Rachele Bettini | Gianfranco Bellipanni
[1] K. Jones,et al. SMADs and YAP compete to control elongation of β-catenin:LEF-1-recruited RNAPII during hESC differentiation. , 2015, Molecular cell.
[2] A. Giordano,et al. The Coiled‐Coil Domain Containing 80 (ccdc80) Gene Regulates gadd45β2 Expression in the Developing Somites of Zebrafish as a New Player of the Hedgehog Pathway , 2015, Journal of cellular physiology.
[3] A. Giordano,et al. The Increase in Maternal Expression of axin1 and axin2 Contribute to the Zebrafish Mutant Ichabod Ventralized Phenotype , 2015, Journal of cellular biochemistry.
[4] U. Nagaraj,et al. Neuroimaging features of Cornelia de Lange syndrome , 2015, Pediatric Radiology.
[5] A. Giordano,et al. FAS/FASL are dysregulated in chordoma and their loss-of-function impairs zebrafish notochord formation , 2014, Oncotarget.
[6] D. Balciunas,et al. Extreme Thermal Noxious Stimuli Induce Pain Responses in Zebrafish Larvae , 2014, Journal of cellular physiology.
[7] C. Tiribelli,et al. Alterations in the Cell Cycle in the Cerebellum of Hyperbilirubinemic Gunn Rat: A Possible Link with Apoptosis? , 2013, PloS one.
[8] L. Garavelli,et al. Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrum , 2013, American journal of medical genetics. Part A.
[9] A. Selicorni,et al. Cornelia de Lange Syndrome: NIPBL haploinsufficiency downregulates canonical Wnt pathway in zebrafish embryos and patients fibroblasts , 2013, Cell Death and Disease.
[10] A. Giordano,et al. The zebrafish as a model for nociception studies , 2013, Journal of cellular physiology.
[11] M. Eccles,et al. Cohesin Is Required for Activation of MYC by Estradiol , 2012, PloS one.
[12] Gabriele Gillessen-Kaesbach,et al. HDAC8 mutations in Cornelia de Lange Syndrome affect the cohesin acetylation cycle , 2012, Nature.
[13] Jacqueline N. Crawley,et al. Autistic-like behavior and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice , 2012, Nature.
[14] I. Krantz,et al. RAD21 mutations cause a human cohesinopathy. , 2012, American journal of human genetics.
[15] K. Shirahige,et al. The Prereplication Complex Recruits XEco2 to Chromatin to Promote Cohesin Acetylation in Xenopus Egg Extracts , 2012, Current Biology.
[16] F. Cotelli,et al. ccdc80-l1 Is Involved in Axon Pathfinding of Zebrafish Motoneurons , 2012, PloS one.
[17] J. Lucas,et al. GSK-3 Mouse Models to Study Neuronal Apoptosis and Neurodegeneration , 2011, Front. Mol. Neurosci..
[18] K. Nasmyth. Cohesin: a catenase with separate entry and exit gates? , 2011, Nature Cell Biology.
[19] A. Lander,et al. Multifactorial Origins of Heart and Gut Defects in nipbl-Deficient Zebrafish, a Model of Cornelia de Lange Syndrome , 2011, PLoS biology.
[20] S. A. Jayakody,et al. Increased Wingless (Wnt) signaling in pituitary progenitor/stem cells gives rise to pituitary tumors in mice and humans , 2011, Proceedings of the National Academy of Sciences.
[21] D. Dorsett. Cohesin: genomic insights into controlling gene transcription and development. , 2011, Current opinion in genetics & development.
[22] David G. Wilkinson,et al. Morpholino artifacts provide pitfalls and reveal a novel role for pro-apoptotic genes in hindbrain boundary development , 2011, Developmental biology.
[23] D. Dorsett,et al. Dosage-Sensitive Regulation of Cohesin Chromosome Binding and Dynamics by Nipped-B, Pds5, and Wapl , 2010, Molecular and Cellular Biology.
[24] G. C. Wagner,et al. Animal model of autism using GSTM1 knockout mice and early post-natal sodium valproate treatment , 2010, Behavioural Brain Research.
[25] I. Krantz,et al. Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey , 2010, American journal of medical genetics. Part A.
[26] E. Weinberg,et al. Molecular dissection of Otx1 functional domains in the zebrafish embryo , 2010, Journal of cellular physiology.
[27] M. Eccles,et al. Expression of cohesin and condensin genes during zebrafish development supports a non-proliferative role for cohesin. , 2009, Gene expression patterns : GEP.
[28] Susan Grepper,et al. Blockade of Wnt-1 signaling leads to anti-tumor effects in hepatocellular carcinoma cells , 2009, Molecular Cancer.
[29] B. Hallgrímsson,et al. Multiple Organ System Defects and Transcriptional Dysregulation in the Nipbl +/− Mouse, a Model of Cornelia de Lange Syndrome , 2009, PLoS genetics.
[30] N. Greene,et al. Apoptosis is not required for mammalian neural tube closure , 2009, Proceedings of the National Academy of Sciences.
[31] Zhe Zhang,et al. Transcriptional Dysregulation in NIPBL and Cohesin Mutant Human Cells , 2009, PLoS biology.
[32] I. Krantz,et al. Dosage Effects of Cohesin Regulatory Factor PDS5 on Mammalian Development: Implications for Cohesinopathies , 2009, PloS one.
[33] D. Colomer,et al. Cyclin D1 mediates resistance to apoptosis through upregulation of molecular chaperones and consequent redistribution of cell death regulators , 2008, Oncogene.
[34] K. Nasmyth,et al. The cohesin ring concatenates sister DNA molecules , 2008, Nature.
[35] R. Ohlsson,et al. Chromatin insulators and cohesins , 2008, EMBO reports.
[36] D. Dorsett. Running rings around chromosomes to trim axons and target dendrites. , 2008, Developmental cell.
[37] C. Lehner,et al. Cell-Type-Specific TEV Protease Cleavage Reveals Cohesin Functions in Drosophila Neurons , 2008, Developmental cell.
[38] S. Maegawa,et al. Chordin expression, mediated by Nodal and FGF signaling, is restricted by redundant function of two β-catenins in the zebrafish embryo , 2007, Mechanisms of Development.
[39] G. Scarano,et al. Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutation , 2007, Clinical genetics.
[40] Kathryn E. Crosier,et al. Cohesin-dependent regulation of Runx genes , 2007, Development.
[41] I. Krantz,et al. Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation. , 2007, American journal of human genetics.
[42] D. Dorsett. Roles of the sister chromatid cohesion apparatus in gene expression, development, and human syndromes , 2007, Chromosoma.
[43] A. Musio,et al. X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations , 2006, Nature Genetics.
[44] R. Balice-Gordon,et al. Neuromuscular synaptogenesis in wild-type and mutant zebrafish. , 2005, Developmental biology.
[45] Nancy Hopkins,et al. Identification of 315 genes essential for early zebrafish development. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[46] I. Krantz,et al. Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B , 2004, Nature Genetics.
[47] I. Krantz,et al. A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3 , 2004, Human Genetics.
[48] Tom Strachan,et al. NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome , 2004, Nature Genetics.
[49] D. Dorsett,et al. Drosophila Nipped-B Protein Supports Sister Chromatid Cohesion and Opposes the Stromalin/Scc3 Cohesion Factor To Facilitate Long-Range Activation of the cut Gene , 2004, Molecular and Cellular Biology.
[50] Thomas D. Schmittgen,et al. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.
[51] C. Albanese,et al. The cyclin D1 gene is a target of the beta-catenin/LEF-1 pathway. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[52] M. Hayashi,et al. Septo-optic dysplasia with cerebellar hypoplasia in Cornelia de Lange syndrome , 1996, Acta Neuropathologica.
[53] J. Postlethwait,et al. Structure of the zebrafish snail1 gene and its expression in wild-type, spadetail and no tail mutant embryos. , 1993, Development.
[54] Amie Y Lee,et al. A monoclonal antibody against Wnt-1 induces apoptosis in human cancer cells. , 2004, Neoplasia.