|DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1|
LA Jerome, VE Papaioannou
Nature genetics 27 (3), 286-291, 2001
|Mammary gland, limb and yolk sac defects in mice lacking Tbx3, the gene mutated in human ulnar mammary syndrome|
TG Davenport, LA Jerome-Majewska, VE Papaioannou
Development 130 (10), 2263-2273, 2003
|The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis|
RG Kelly, LA Jerome-Majewska, VE Papaioannou
Human molecular genetics 13 (22), 2829-2840, 2004
|High intake of folic acid disrupts embryonic development in mice|
L Pickell, K Brown, D Li, XL Wang, L Deng, Q Wu, J Selhub, L Luo, ...
Birth Defects Research Part A: Clinical and Molecular Teratology 91 (1), 8-19, 2011
|Tbx3, the ulnar‐mammary syndrome gene, and Tbx2 interact in mammary gland development through a p19Arf/p53‐independent pathway|
LA Jerome‐Majewska, GP Jenkins, E Ernstoff, F Zindy, CJ Sherr, ...
Developmental dynamics: an official publication of the American Association …, 2005
|Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11. 2DS|
DM McDonald-McGinn, S Fahiminiya, T Revil, BA Nowakowska, J Suhl, ...
Journal of medical genetics 50 (2), 80-90, 2013
|Alternative splicing is frequent during early embryonic development in mouse|
T Revil, D Gaffney, C Dias, J Majewski, LA Jerome-Majewska
BMC genomics 11 (1), 399, 2010
|Methylenetetrahydrofolate reductase deficiency and low dietary folate increase embryonic delay and placental abnormalities in mice|
L Pickell, D Li, K Brown, LG Mikael, XL Wang, Q Wu, L Luo, ...
Birth Defects Research Part A: Clinical and Molecular Teratology 85 (6), 531-541, 2009
|Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development|
F Moraes, A Nóvoa, LA Jerome-Majewska, VE Papaioannou, M Mallo
Mechanisms of development 122 (2), 199-212, 2005
|Mutations in SCARF2 are responsible for Van Den Ende-Gupta syndrome|
N Anastasio, T Ben-Omran, A Teebi, KCH Ha, E Lalonde, R Ali, ...
The American Journal of Human Genetics 87 (4), 553-559, 2010
|The trafficking protein Tmed2/p24β1 is required for morphogenesis of the mouse embryo and placenta|
LA Jerome-Majewska, T Achkar, L Luo, F Lupu, E Lacy
Developmental biology 341 (1), 154-166, 2010
|Aortic arch and pharyngeal phenotype in the absence of BMP-dependent neural crest in the mouse|
S Ohnemus, B Kanzler, LA Jerome-Majewska, VE Papaioannou, ...
Mechanisms of development 119 (2), 127-135, 2002
|Barriers to horizontal cell transformation by extracellular vesicles containing oncogenic H-ras|
TH Lee, S Chennakrishnaiah, B Meehan, L Montermini, D Garnier, ...
Oncotarget 7 (32), 51991, 2016
|Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro–costo–mandibular syndrome|
DC Lynch, T Revil, J Schwartzentruber, EJ Bhoj, AM Innes, RE Lamont, ...
Nature communications 5 (1), 1-6, 2014
|A novel mouse model for genetic variation in 10-formyltetrahydrofolate synthetase exhibits disturbed purine synthesis with impacts on pregnancy and embryonic development|
KE Christensen, L Deng, KY Leung, E Arning, T Bottiglieri, OV Malysheva, ...
Human molecular genetics 22 (18), 3705-3719, 2013
|Vitamin B12 metabolism during pregnancy and in embryonic mouse models|
MA Moreno-Garcia, DS Rosenblatt, LA Jerome-Majewska
Nutrients 5 (9), 3531-3550, 2013
|During Embryogenesis, Esrp1 Expression Is Restricted to a Subset of Epithelial Cells and Is Associated With Splicing of a Number of Developmentally Important …|
T Revil, LA Jerome‐Majewska
Developmental Dynamics 242 (3), 281-290, 2013
|TMED2/p24β1 is expressed in all gestational stages of human placentas and in choriocarcinoma cell lines|
A Zakariyah, W Hou, R Slim, L Jerome-Majewska
Placenta 33 (3), 214-219, 2012
|Moderate folic acid supplementation and MTHFD1-synthetase deficiency in mice, a model for the R653Q variant, result in embryonic defects and abnormal placental development|
KE Christensen, W Hou, RH Bahous, L Deng, OV Malysheva, E Arning, ...
The American journal of clinical nutrition 104 (5), 1459-1469, 2016
|Somatic overgrowth associated with homozygous mutations in both MAN1B1 and SEC23A|
S Gupta, S Fahiminiya, T Wang, LD Nunez, DS Rosenblatt, WT Gibson, ...
Molecular Case Studies 2 (3), a000737, 2016