Tessarollo L - Search Results

1

Berthet C, Aleem E, Coppola V, Tessarollo L, Kaldis P. Berthet C, et al. Among authors: tessarollo l. Curr Biol. 2003 Oct 14;13(20):1775-85. doi: 10.1016/j.cub.2003.09.024. Curr Biol. 2003. PMID: 14561402 Free article.

2

Evidence for a role of truncated trkC receptor isoforms in mouse development.

Palko ME, Coppola V, Tessarollo L. Palko ME, et al. Among authors: tessarollo l. J Neurosci. 1999 Jan 15;19(2):775-82. doi: 10.1523/JNEUROSCI.19-02-00775.1999. J Neurosci. 1999. PMID: 9880597 Free PMC article.

3

Brain-derived neurotrophic factor-deficient mice develop aggressiveness and hyperphagia in conjunction with brain serotonergic abnormalities.

Lyons WE, Mamounas LA, Ricaurte GA, Coppola V, Reid SW, Bora SH, Wihler C, Koliatsos VE, Tessarollo L. Lyons WE, et al. Among authors: tessarollo l. Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):15239-44. doi: 10.1073/pnas.96.26.15239. Proc Natl Acad Sci U S A. 1999. PMID: 10611369 Free PMC article.

4

Targeted disruption of the Nijmegen breakage syndrome gene NBS1 leads to early embryonic lethality in mice.

Zhu J, Petersen S, Tessarollo L, Nussenzweig A. Zhu J, et al. Among authors: tessarollo l. Curr Biol. 2001 Jan 23;11(2):105-9. doi: 10.1016/s0960-9822(01)00019-7. Curr Biol. 2001. PMID: 11231126 Free article.

5

Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice.

Wilson SM, Householder DB, Coppola V, Tessarollo L, Fritzsch B, Lee EC, Goss D, Carlson GA, Copeland NG, Jenkins NA. Wilson SM, et al. Among authors: tessarollo l. Genomics. 2001 Jun 1;74(2):228-33. doi: 10.1006/geno.2001.6554. Genomics. 2001. PMID: 11386759

6

Dissection of NT3 functions in vivo by gene replacement strategy.

Coppola V, Kucera J, Palko ME, Martinez-De Velasco J, Lyons WE, Fritzsch B, Tessarollo L. Coppola V, et al. Among authors: tessarollo l. Development. 2001 Nov;128(21):4315-27. doi: 10.1242/dev.128.21.4315. Development. 2001. PMID: 11684666

7

Genomic instability in mice lacking histone H2AX.

Celeste A, Petersen S, Romanienko PJ, Fernandez-Capetillo O, Chen HT, Sedelnikova OA, Reina-San-Martin B, Coppola V, Meffre E, Difilippantonio MJ, Redon C, Pilch DR, Olaru A, Eckhaus M, Camerini-Otero RD, Tessarollo L, Livak F, Manova K, Bonner WM, Nussenzweig MC, Nussenzweig A. Celeste A, et al. Among authors: tessarollo l. Science. 2002 May 3;296(5569):922-7. doi: 10.1126/science.1069398. Epub 2002 Apr 4. Science. 2002. PMID: 11934988 Free PMC article.

8

Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease.

Wilson SM, Bhattacharyya B, Rachel RA, Coppola V, Tessarollo L, Householder DB, Fletcher CF, Miller RJ, Copeland NG, Jenkins NA. Wilson SM, et al. Among authors: tessarollo l. Nat Genet. 2002 Nov;32(3):420-5. doi: 10.1038/ng1006. Epub 2002 Oct 7. Nat Genet. 2002. PMID: 12368914

9

BRCA2 deficiency in mice leads to meiotic impairment and infertility.

Sharan SK, Pyle A, Coppola V, Babus J, Swaminathan S, Benedict J, Swing D, Martin BK, Tessarollo L, Evans JP, Flaws JA, Handel MA. Sharan SK, et al. Among authors: tessarollo l. Development. 2004 Jan;131(1):131-42. doi: 10.1242/dev.00888. Epub 2003 Dec 3. Development. 2004. PMID: 14660434

10

NT-3 replacement with brain-derived neurotrophic factor redirects vestibular nerve fibers to the cochlea.

Tessarollo L, Coppola V, Fritzsch B. Tessarollo L, et al. J Neurosci. 2004 Mar 10;24(10):2575-84. doi: 10.1523/JNEUROSCI.5514-03.2004. J Neurosci. 2004. PMID: 15014133 Free PMC article.

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