Jerome-Majewska LA - Search Results

1

Sf3b4 regulates chromatin remodeler splicing and Hox expression.

Kumar S, Alam SS, Bareke E, Beauchamp MC, Dong Y, Chan W, Majewski J, Jerome-Majewska LA. Kumar S, et al. Among authors: jerome majewska la. Differentiation. 2023 May-Jun;131:59-73. doi: 10.1016/j.diff.2023.04.004. Epub 2023 May 4. Differentiation. 2023. PMID: 37167859

2

Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development.

Moraes F, Nóvoa A, Jerome-Majewska LA, Papaioannou VE, Mallo M. Moraes F, et al. Mech Dev. 2005 Feb;122(2):199-212. doi: 10.1016/j.mod.2004.10.004. Mech Dev. 2005. PMID: 15652707 Free article.

3

Tbx3, the ulnar-mammary syndrome gene, and Tbx2 interact in mammary gland development through a p19Arf/p53-independent pathway.

Jerome-Majewska LA, Jenkins GP, Ernstoff E, Zindy F, Sherr CJ, Papaioannou VE. Jerome-Majewska LA, et al. Dev Dyn. 2005 Dec;234(4):922-33. doi: 10.1002/dvdy.20575. Dev Dyn. 2005. PMID: 16222716 Free article.

4

Mammary gland, limb and yolk sac defects in mice lacking Tbx3, the gene mutated in human ulnar mammary syndrome.

Davenport TG, Jerome-Majewska LA, Papaioannou VE. Davenport TG, et al. Development. 2003 May;130(10):2263-73. doi: 10.1242/dev.00431. Development. 2003. PMID: 12668638

5

Aortic arch and pharyngeal phenotype in the absence of BMP-dependent neural crest in the mouse.

Ohnemus S, Kanzler B, Jerome-Majewska LA, Papaioannou VE, Boehm T, Mallo M. Ohnemus S, et al. Mech Dev. 2002 Dec;119(2):127-35. doi: 10.1016/s0925-4773(02)00345-3. Mech Dev. 2002. PMID: 12464426 Free article.

6

The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis.

Kelly RG, Jerome-Majewska LA, Papaioannou VE. Kelly RG, et al. Hum Mol Genet. 2004 Nov 15;13(22):2829-40. doi: 10.1093/hmg/ddh304. Epub 2004 Sep 22. Hum Mol Genet. 2004. PMID: 15385444

7

Alternative splicing is frequent during early embryonic development in mouse.

Revil T, Gaffney D, Dias C, Majewski J, Jerome-Majewska LA. Revil T, et al. BMC Genomics. 2010 Jun 23;11:399. doi: 10.1186/1471-2164-11-399. BMC Genomics. 2010. PMID: 20573213 Free PMC article.

8

Mutations in SCARF2 are responsible for Van Den Ende-Gupta syndrome.

Anastasio N, Ben-Omran T, Teebi A, Ha KC, Lalonde E, Ali R, Almureikhi M, Der Kaloustian VM, Liu J, Rosenblatt DS, Majewski J, Jerome-Majewska LA. Anastasio N, et al. Am J Hum Genet. 2010 Oct 8;87(4):553-9. doi: 10.1016/j.ajhg.2010.09.005. Am J Hum Genet. 2010. PMID: 20887961 Free PMC article.

9

Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro-costo-mandibular syndrome.

Lynch DC, Revil T, Schwartzentruber J, Bhoj EJ, Innes AM, Lamont RE, Lemire EG, Chodirker BN, Taylor JP, Zackai EH, McLeod DR, Kirk EP, Hoover-Fong J, Fleming L, Savarirayan R; Care4Rare Canada; Majewski J, Jerome-Majewska LA, Parboosingh JS, Bernier FP. Lynch DC, et al. Nat Commun. 2014 Jul 22;5:4483. doi: 10.1038/ncomms5483. Nat Commun. 2014. PMID: 25047197 Free PMC article.

10

Non-alcoholic fatty liver disease in mice with heterozygous mutation in TMED2.

Hou W, Gupta S, Beauchamp MC, Yuan L, Jerome-Majewska LA. Hou W, et al. PLoS One. 2017 Aug 10;12(8):e0182995. doi: 10.1371/journal.pone.0182995. eCollection 2017. PLoS One. 2017. PMID: 28797121 Free PMC article.

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