Antonio Baldini
Antonio Baldini
Department of Molecular Medicine and Medical Biotech., University Federico II, Naples, Italy
Verified email at unina.it
Title
Cited by
Cited by
Year
p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene.
S Matsuoka, MC Edwards, C Bai, S Parker, P Zhang, A Baldini, JW Harper, ...
Genes & development 9 (6), 650-662, 1995
11601995
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice
EA Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, ...
Nature 410 (6824), 97-101, 2001
9172001
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia
B Lee, K Thirunavukkarasu, L Zhou, L Pastore, A Baldini, J Hecht, ...
Nature genetics 16 (3), 307-310, 1997
5901997
Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy
T Ried, A Baldini, TC Rand, DC Ward
Proceedings of the National Academy of Sciences 89 (4), 1388-1392, 1992
5161992
Improved telomere detection using a telomere repeat probe (TTAGGG) n generated by PCR.
JW Ijdo, RA Wells, A Baldini, ST Reeders
Nucleic acids research 19 (17), 4780, 1991
5131991
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome
SD Dreyer, G Zhou, A Baldini, A Winterpacht, B Zabel, W Cole, ...
Nature genetics 19 (1), 47-50, 1998
4811998
Congenital heart disease in mice deficient for the DiGeorge syndrome region
EA Lindsay, A Botta, V Jurecic, S Carattini-Rivera, YC Cheah, ...
Nature 401 (6751), 379-383, 1999
3931999
Origin of human chromosome 2: an ancestral telomere-telomere fusion.
JW Ijdo, A Baldini, DC Ward, ST Reeders, RA Wells
Proceedings of the National Academy of Sciences 88 (20), 9051-9055, 1991
3851991
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract
H Xu, M Morishima, JN Wylie, RJ Schwartz, BG Bruneau, EA Lindsay, ...
Development 131 (13), 3217-3227, 2004
3582004
A pivotal role for endogenous TGF-β-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway
M Xie, D Zhang, JRB Dyck, Y Li, H Zhang, M Morishima, DL Mann, ...
Proceedings of the National Academy of Sciences 103 (46), 17378-17383, 2006
3532006
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways
F Vitelli, M Morishima, I Taddei, EA Lindsay, A Baldini
Human molecular genetics 11 (8), 915-922, 2002
3202002
A genetic link between Tbx1 and fibroblast growth factor signaling
F Vitelli, I Taddei, M Morishima, EN Meyers, EA Lindsay, A Baldini
Development 129 (19), 4605-4611, 2002
2852002
Human acetyl-CoA carboxylase 2 molecular cloning, characterization, chromosomal mapping, and evidence for two isoforms
L Abu-Elheiga, DB Almarza-Ortega, A Baldini, SJ Wakil
Journal of Biological Chemistry 272 (16), 10669-10677, 1997
2581997
Human acetyl-CoA carboxylase: characterization, molecular cloning, and evidence for two isoforms.
L Abu-Elheiga, A Jayakumar, A Baldini, SS Chirala, SJ Wakil
Proceedings of the National Academy of Sciences 92 (9), 4011-4015, 1995
2071995
DOC-2, a candidate tumor suppressor gene in human epithelial ovarian cancer
SC Mok, WY Chan, KK Wong, KK Cheung, CC Lau, SW Ng, A Baldini, ...
Oncogene 16 (18), 2381-2387, 1998
1931998
Identification of a gene that reverses the immortal phenotype of a subset of cells and is a member of a novel family of transcription factor-like genes
MJ Bertram, NG Berube, X Hang-Swanson, Q Ran, JK Leung, S Bryce, ...
Molecular and cellular biology 19 (2), 1479-1485, 1999
1771999
Canonical Wnt signaling functions in second heart field to promote right ventricular growth
D Ai, X Fu, J Wang, MF Lu, L Chen, A Baldini, WH Klein, JF Martin
Proceedings of the National Academy of Sciences 104 (22), 9319-9324, 2007
1752007
Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development
Z Zhang, T Huynh, A Baldini
Development 133 (18), 3587-3595, 2006
1672006
Molecular analyses of 17p11. 2 deletions in 62 Smith-Magenis syndrome patients.
RC Juyal, LE Figuera, X Hauge, SH Elsea, JR Lupski, F Greenberg, ...
American journal of human genetics 58 (5), 998, 1996
1571996
Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity
EE Eichler, ML Budarf, M Rocchi, LL Deaven, NA Doggett, A Baldini, ...
Human molecular genetics 6 (7), 991-1002, 1997
1551997
The system can't perform the operation now. Try again later.
Articles 1–20