Loydie A. Jerome-Majewska
Loydie A. Jerome-Majewska
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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
Oxford University Press for The Company of Biologists Limited 130 (10), 2263 …, 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
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
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
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
Alternative splicing is frequent during early embryonic development in mouse
T Revil, D Gaffney, C Dias, J Majewski, LA Jerome-Majewska
BMC genomics 11, 1-17, 2010
Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation
CB Gurumurthy, AR O’brien, RM Quadros, J Adams, P Alcaide, S Ayabe, ...
Genome biology 20 (1), 1-14, 2019
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
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
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), 4483, 2014
Control of anterior GR adient 2 (AGR 2) dimerization links endoplasmic reticulum proteostasis to inflammation
M Maurel, J Obacz, T Avril, YP Ding, O Papadodima, X Treton, F Daniel, ...
EMBO molecular medicine 11 (6), e10120, 2019
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
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
Transmembrane emp24 domain proteins in development and disease.
R Aber, W Chan, S Mugisha, LA Jerome-Majewska
Genetics Research 101, e14, 2019
Spliceosomopathies and neurocristopathies: Two sides of the same coin?
MC Beauchamp, SS Alam, S Kumar, LA Jerome‐Majewska
Developmental Dynamics 249 (8), 924-945, 2020
Non-alcoholic fatty liver disease in mice with heterozygous mutation in TMED2
W Hou, S Gupta, MC Beauchamp, L Yuan, LA Jerome-Majewska
PLoS One 12 (8), e0182995, 2017
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