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Luca Cartegni
Luca Cartegni
Associate Professor, Chemical Biology, School of Pharmacy, Rutgers University
Verified email at pharmacy.rutgers.edu - Homepage
Title
Cited by
Cited by
Year
Listening to silence and understanding nonsense: exonic mutations that affect splicing
L Cartegni, SL Chew, AR Krainer
Nature reviews genetics 3 (4), 285-298, 2002
27442002
ESEfinder: a web resource to identify exonic splicing enhancers
L Cartegni, J Wang, Z Zhu, MQ Zhang, AR Krainer
Nucleic acids research 31 (13), 3568-3571, 2003
18462003
Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1
L Cartegni, AR Krainer
Nature genetics 30 (4), 377-384, 2002
9272002
A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes
HX Liu, L Cartegni, MQ Zhang, AR Krainer
Nature genetics 27 (1), 55-58, 2001
5932001
Correction of disease-associated exon skipping by synthetic exon-specific activators
L Cartegni, AR Krainer
Nature structural biology 10 (2), 120-125, 2003
3782003
Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2
L Cartegni, ML Hastings, JA Calarco, E de Stanchina, AR Krainer
The American Journal of Human Genetics 78 (1), 63-77, 2006
3702006
Exonic splicing enhancer motif recognized by human SC35 under splicing conditions
HX Liu, SL Chew, L Cartegni, MQ Zhang, AR Krainer
Molecular and cellular biology 20 (3), 1063-1071, 2000
2922000
hnRNP A1 selectively interacts through its Gly-rich domain with different RNA-binding proteins
L Cartegni, M Maconi, E Morandi, F Cobianchi, S Riva, G Biamonti
Journal of molecular biology 259 (3), 337-348, 1996
2401996
Splicing factor hnRNPH drives an oncogenic splicing switch in gliomas
CV LeFave, M Squatrito, S Vorlova, GL Rocco, CW Brennan, EC Holland, ...
The EMBO journal 30 (19), 4084-4097, 2011
1862011
Antitumorigenic potential of STAT3 alternative splicing modulation
F Zammarchi, E de Stanchina, E Bournazou, T Supakorndej, K Martires, ...
Proceedings of the National Academy of Sciences 108 (43), 17779-17784, 2011
1772011
Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy
L Cartegni, MR di Barletta, R Barresi, S Squarzoni, P Sabatelli, N Maraldi, ...
Human molecular genetics 6 (13), 2257-2264, 1997
1631997
Seemingly neutral polymorphic variants may confer immunity to splicing-inactivating mutations: a synonymous SNP in exon 5 of MCAD protects from deleterious mutations in a …
KB Nielsen, S Sørensen, L Cartegni, TJ Corydon, TK Doktor, ...
The American Journal of Human Genetics 80 (3), 416-432, 2007
1552007
Induction of antagonistic soluble decoy receptor tyrosine kinases by intronic polyA activation
S Vorlová, G Rocco, CV LeFave, FM Jodelka, K Hess, ML Hastings, ...
Molecular cell 43 (6), 927-939, 2011
1542011
A novel hnRNP protein (HAP/SAF-B) enters a subset of hnRNP complexes and relocates in nuclear granules in response to heat shock
F Weighardt, F Cobianchi, L Cartegni, I Chiodi, A Villa, S Riva, G Biamonti
Journal of cell science 112 (10), 1465-1476, 2000
1532000
Peptide-conjugated antisense oligonucleotides for targeted inhibition of a transcriptional regulator in vivo
E Henke, J Perk, J Vider, P De Candia, Y Chin, DB Solit, V Ponomarev, ...
Nature biotechnology 26 (1), 91-100, 2008
1372008
BRCA2 T2722R is a deleterious allele that causes exon skipping
JD Fackenthal, L Cartegni, AR Krainer, OI Olopade
The American Journal of Human Genetics 71 (3), 625-631, 2002
1162002
Therapeutic hemoglobin levels after gene transfer in β-thalassemia mice and in hematopoietic cells of β-thalassemia and sickle cells disease patients
L Breda, C Casu, S Gardenghi, N Bianchi, L Cartegni, M Narla, ...
PloS one 7 (3), e32345, 2012
1072012
KLF4 is a novel candidate tumor suppressor gene in pancreatic ductal carcinoma
F Zammarchi, M Morelli, M Menicagli, C Di Cristofano, K Zavaglia, ...
The American journal of pathology 178 (1), 361-372, 2011
962011
p53Ψ is a transcriptionally inactive p53 isoform able to reprogram cells toward a metastatic-like state
S Senturk, Z Yao, M Camiolo, B Stiles, T Rathod, AM Walsh, ...
Proceedings of the National Academy of Sciences 111 (32), E3287-E3296, 2014
912014
X‐linked emery‐dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample
M Mora, L Cartegni, C Di Blasi, R Barresi, S Bione, MR di Barletta, ...
Annals of Neurology: Official Journal of the American Neurological …, 1997
721997
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