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Elizabeth Illingworth
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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
11032001
Timing of surgery following SARS‐CoV‐2 infection: an international prospective cohort study
H Gacaferi, GS Collaborative, COVIDSurg Collaborative
Anaesthesia 76 (6), 2021
528*2021
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus
PJ Scambler, D Kelly, E Lindsay, R Williamson, R Goldberg, R Shprintzen, ...
The Lancet 339 (8802), 1138-1139, 1992
5041992
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
4701999
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, ...
Oxford University Press for The Company of Biologists Limited 131 (13), 3217 …, 2004
4282004
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
3782002
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome
R Paylor, B Glaser, A Mupo, P Ataliotis, C Spencer, A Sobotka, C Sparks, ...
Proceedings of the National Academy of Sciences 103 (20), 7729-7734, 2006
3392006
Chromosomal microdeletions: dissecting del22q11 syndrome
EA Lindsay
Nature Reviews Genetics 2 (11), 858-868, 2001
3212001
A genetic link between Tbx1 and fibroblast growth factor signaling
F Vitelli, I Taddei, M Morishima, EN Meyers, EA Lindsay, A Baldini
Oxford University Press for The Company of Biologists Limited 129 (19), 4605 …, 2002
3202002
Confirmation that the velo‐cardio‐facial syndrome is associated with haplo‐insufficiency of genes at chromosome 22q11
D Kelly, R Goldberg, D Wilson, E Lindsay, A Carey, J Goodship, J Burn, ...
American journal of medical genetics 45 (3), 308-312, 1993
1941993
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments
R Paylor, KL McIlwain, R McAninch, A Nellis, LA Yuva-Paylor, A Baldini, ...
Human molecular genetics 10 (23), 2645-2650, 2001
1662001
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease
S Halford, R Wadey, C Roberts, SCM Daw, JA Whiting, H O'Donnell, ...
Human molecular genetics 2 (12), 2099-2107, 1993
1651993
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice
V Randall, K McCue, C Roberts, V Kyriakopoulou, S Beddow, AN Barrett, ...
The Journal of clinical investigation 119 (11), 3301-3310, 2009
1612009
Velo‐cardio‐facial syndrome: Frequency and extent of 22q1l deletions
EA Lindsay, R Goldberg, V Jurecic, B Morrow, C Carlson, ...
American journal of medical genetics 57 (3), 514-522, 1995
1571995
TBX1 is required for inner ear morphogenesis
F Vitelli, A Viola, M Morishima, T Pramparo, A Baldini, E Lindsay
Human molecular genetics 12 (16), 2041-2048, 2003
1482003
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm
A Calmont, S Ivins, KL Van Bueren, I Papangeli, V Kyriakopoulou, ...
Development 136 (18), 3173-3183, 2009
1442009
Submicroscopic deletions at 22q11. 2: variability of the clinical picture and delineation of a commonly deleted region
EA Lindsay, F Greenberg, LG Shaffer, SK Shapira, PJ Scambler, A Baldini
American journal of medical genetics 56 (2), 191-197, 1995
1441995
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development
Z Zhang, F Cerrato, H Xu, F Vitelli, M Morishima, J Vincentz, Y Furuta, ...
Oxford University Press for The Company of Biologists Limited 132 (23), 5307 …, 2005
1412005
Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes
I Taddei, M Morishima, T Huynh, EA Lindsay
Proceedings of the National Academy of Sciences 98 (20), 11428-11431, 2001
1272001
A genetic etiology for interruption of the aortic arch type B
MB Lewin, EA Lindsay, V Jurecic, V Goytia, JA Towbin, A Baldini
The American journal of cardiology 80 (4), 493-497, 1997
1271997
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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