Hager E - Search Results

1

Neurotransmitter alterations in embryonic succinate semialdehyde dehydrogenase (SSADH) deficiency suggest a heightened excitatory state during development.

Jansen EE, Struys E, Jakobs C, Hager E, Snead OC, Gibson KM. Jansen EE, et al. Among authors: hager e. BMC Dev Biol. 2008 Nov 28;8:112. doi: 10.1186/1471-213X-8-112. BMC Dev Biol. 2008. PMID: 19040727 Free PMC article.

2

Hepatocyte transplantation (HTx) corrects selected neurometabolic abnormalities in murine intermediate maple syrup urine disease (iMSUD).

Skvorak KJ, Hager EJ, Arning E, Bottiglieri T, Paul HS, Strom SC, Homanics GE, Sun Q, Jansen EE, Jakobs C, Zinnanti WJ, Gibson KM. Skvorak KJ, et al. Among authors: hager ej. Biochim Biophys Acta. 2009 Oct;1792(10):1004-10. doi: 10.1016/j.bbadis.2009.08.006. Epub 2009 Aug 19. Biochim Biophys Acta. 2009. PMID: 19699299 Free PMC article.

3

Mevalonate kinase deficiency and autoinflammation.

Hager EJ, Gibson KM. Hager EJ, et al. N Engl J Med. 2007 Nov 1;357(18):1871-2. doi: 10.1056/NEJMc072799. N Engl J Med. 2007. PMID: 17978300 No abstract available.

4

Deletion of a single mevalonate kinase (Mvk) allele yields a murine model of hyper-IgD syndrome.

Hager EJ, Tse HM, Piganelli JD, Gupta M, Baetscher M, Tse TE, Pappu AS, Steiner RD, Hoffmann GF, Gibson KM. Hager EJ, et al. J Inherit Metab Dis. 2007 Nov;30(6):888-95. doi: 10.1007/s10545-007-0776-7. Epub 2007 Nov 19. J Inherit Metab Dis. 2007. PMID: 18008182

5

Aberrant expression of costimulatory molecules in splenocytes of the mevalonate kinase-deficient mouse model of human hyper-IgD syndrome (HIDS).

Hager EJ, Piganelli JD, Tse HM, Gibson KM. Hager EJ, et al. J Inherit Metab Dis. 2012 Jan;35(1):159-68. doi: 10.1007/s10545-011-9349-x. Epub 2011 May 24. J Inherit Metab Dis. 2012. PMID: 21607759 Free PMC article.

6

Long chain fatty acid (Lcfa) abnormalities in hyper Igd syndrome (Hids) and Familial Mediterranean Fever (Fmf): new insight into heritable periodic fevers.

Simon A, Drenth JP, Matern D, Goetzman ES, Hager EJ, Gibson KM. Simon A, et al. Mol Genet Metab. 2013 Mar;108(3):166-71. doi: 10.1016/j.ymgme.2013.01.004. Epub 2013 Jan 15. Mol Genet Metab. 2013. PMID: 23375471 Free PMC article.

7

Identification and characterization of spdR mutations that bypass the BsgA protease-dependent regulation of developmental gene expression in Myxococcus xanthus.

Hager E, Tse H, Gill RE. Hager E, et al. Mol Microbiol. 2001 Feb;39(3):765-80. doi: 10.1046/j.1365-2958.2001.02266.x. Mol Microbiol. 2001. PMID: 11169116 Free article.

8

Developmentally regulated expression of three slow isoforms of myosin heavy chain: diversity among the first fibers to form in avian muscle.

Page S, Miller JB, DiMario JX, Hager EJ, Moser A, Stockdale FE. Page S, et al. Among authors: hager ej. Dev Biol. 1992 Nov;154(1):118-28. doi: 10.1016/0012-1606(92)90053-j. Dev Biol. 1992. PMID: 1426621 Free article.

9

Characterization of bcsA mutations that bypass two distinct signaling requirements for Myxococcus xanthus development.

Cusick JK, Hager E, Gill RE. Cusick JK, et al. Among authors: hager e. J Bacteriol. 2002 Sep;184(18):5141-50. doi: 10.1128/JB.184.18.5141-5150.2002. J Bacteriol. 2002. PMID: 12193631 Free PMC article.

10

Identification of a mutant locus that bypasses the BsgA protease requirement for social development in Myxococcus xanthus.

Cusick JK, Hager E, Gill RE. Cusick JK, et al. Among authors: hager e. FEMS Microbiol Lett. 2015 Jan;362(1):1-8. doi: 10.1093/femsle/fnu028. Epub 2014 Dec 4. FEMS Microbiol Lett. 2015. PMID: 25790505

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