Carpinelli MR - Search Results

1

Vitamin D-deficient diet rescues hearing loss in Klotho mice.

Carpinelli MR, Wise AK, Burt RA. Carpinelli MR, et al. Hear Res. 2011 May;275(1-2):105-9. doi: 10.1016/j.heares.2010.12.009. Epub 2010 Dec 16. Hear Res. 2011. PMID: 21167925

2

Anti-apoptotic gene Bcl2 is required for stapes development and hearing.

Carpinelli MR, Wise AK, Arhatari BD, Bouillet P, Manji SS, Manning MG, Cooray AA, Burt RA. Carpinelli MR, et al. Cell Death Dis. 2012 Aug 9;3(8):e362. doi: 10.1038/cddis.2012.100. Cell Death Dis. 2012. PMID: 22874999 Free PMC article.

3

Two ENU-induced alleles of Atp2b2 cause deafness in mice.

Carpinelli MR, Manning MG, Kile BT, Burt RA. Carpinelli MR, et al. PLoS One. 2013 Jun 24;8(6):e67479. doi: 10.1371/journal.pone.0067479. Print 2013. PLoS One. 2013. PMID: 23826306 Free PMC article.

4

A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination.

Carpinelli MR, Voss AK, Manning MG, Perera AA, Cooray AA, Kile BT, Burt RA. Carpinelli MR, et al. Dis Model Mech. 2014 Jun;7(6):649-57. doi: 10.1242/dmm.014605. Epub 2014 Mar 28. Dis Model Mech. 2014. PMID: 24682784 Free PMC article.

5

CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairment.

Ogier JM, Carpinelli MR, Arhatari BD, Symons RC, Kile BT, Burt RA. Ogier JM, et al. Among authors: carpinelli mr. PLoS One. 2014 May 19;9(5):e97559. doi: 10.1371/journal.pone.0097559. eCollection 2014. PLoS One. 2014. PMID: 24840056 Free PMC article.

6

Genetic Modifier Screens in Mice.

Carpinelli MR, Burt RA, Kile BT. Carpinelli MR, et al. Curr Protoc Mouse Biol. 2012 Mar 1;2(1):75-87. doi: 10.1002/9780470942390.mo110161. Curr Protoc Mouse Biol. 2012. PMID: 26069006

7

Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen Syndrome.

Carpinelli MR, Kruse EA, Arhatari BD, Debrincat MA, Ogier JM, Bories JC, Kile BT, Burt RA. Carpinelli MR, et al. Am J Pathol. 2015 Jul;185(7):1867-76. doi: 10.1016/j.ajpath.2015.03.026. Am J Pathol. 2015. PMID: 26093983 Free article.

8

An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome.

Ogier JM, Arhatari BD, Carpinelli MR, McColl BK, Wilson MA, Burt RA. Ogier JM, et al. Among authors: carpinelli mr. Sci Rep. 2018 Apr 3;8(1):5482. doi: 10.1038/s41598-018-23856-8. Sci Rep. 2018. PMID: 29615807 Free PMC article.

9

An ethyl-nitrosourea-induced point mutation in phex causes exon skipping, x-linked hypophosphatemia, and rickets.

Carpinelli MR, Wicks IP, Sims NA, O'Donnell K, Hanzinikolas K, Burt R, Foote SJ, Bahlo M, Alexander WS, Hilton DJ. Carpinelli MR, et al. Am J Pathol. 2002 Nov;161(5):1925-33. doi: 10.1016/S0002-9440(10)64468-9. Am J Pathol. 2002. PMID: 12414538 Free PMC article.

10

Thrombocytopenia and kidney disease in mice with a mutation in the C1galt1 gene.

Alexander WS, Viney EM, Zhang JG, Metcalf D, Kauppi M, Hyland CD, Carpinelli MR, Stevenson W, Croker BA, Hilton AA, Ellis S, Selan C, Nandurkar HH, Goodnow CC, Kile BT, Nicola NA, Roberts AW, Hilton DJ. Alexander WS, et al. Among authors: carpinelli mr. Proc Natl Acad Sci U S A. 2006 Oct 31;103(44):16442-7. doi: 10.1073/pnas.0607872103. Epub 2006 Oct 24. Proc Natl Acad Sci U S A. 2006. PMID: 17062753 Free PMC article.

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