Meroni G - Search Results

1

X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum.

De Falco F, Cainarca S, Andolfi G, Ferrentino R, Berti C, Rodríguez Criado G, Rittinger O, Dennis N, Odent S, Rastogi A, Liebelt J, Chitayat D, Winter R, Jawanda H, Ballabio A, Franco B, Meroni G. De Falco F, et al. Among authors: meroni g. Am J Med Genet A. 2003 Jul 15;120A(2):222-8. doi: 10.1002/ajmg.a.10265. Am J Med Genet A. 2003. PMID: 12833403 Review.

2

Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubules.

Berti C, Fontanella B, Ferrentino R, Meroni G. Berti C, et al. Among authors: meroni g. BMC Cell Biol. 2004 Feb 29;5:9. doi: 10.1186/1471-2121-5-9. BMC Cell Biol. 2004. PMID: 15070402 Free PMC article.

3

MID1 mutation screening in a large cohort of Opitz G/BBB syndrome patients: twenty-nine novel mutations identified.

Ferrentino R, Bassi MT, Chitayat D, Tabolacci E, Meroni G. Ferrentino R, et al. Among authors: meroni g. Hum Mutat. 2007 Feb;28(2):206-7. doi: 10.1002/humu.9480. Hum Mutat. 2007. PMID: 17221865

4

X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE gene.

Parenti G, Buttitta P, Meroni G, Franco B, Bernard L, Rizzolo MG, Brunetti-Pierri N, Ballabio A, Andria G. Parenti G, et al. Among authors: meroni g. Am J Med Genet. 1997 Dec 12;73(2):139-43. doi: 10.1002/(sici)1096-8628(19971212)73:2<139::aid-ajmg7>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9409863

5

TRIM9 is specifically expressed in the embryonic and adult nervous system.

Berti C, Messali S, Ballabio A, Reymond A, Meroni G. Berti C, et al. Among authors: meroni g. Mech Dev. 2002 May;113(2):159-62. doi: 10.1016/s0925-4773(02)00013-8. Mech Dev. 2002. PMID: 11960705 Free article.

6

X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variability.

Brunetti-Pierri N, Andreucci MV, Tuzzi R, Vega GR, Gray G, McKeown C, Ballabio A, Andria G, Meroni G, Parenti G. Brunetti-Pierri N, et al. Among authors: meroni g. Am J Med Genet A. 2003 Mar 1;117A(2):164-8. doi: 10.1002/ajmg.a.10950. Am J Med Genet A. 2003. PMID: 12567415

7

Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermis.

Lancioni A, Pizzo M, Fontanella B, Ferrentino R, Napolitano LM, De Leonibus E, Meroni G. Lancioni A, et al. Among authors: meroni g. J Neurosci. 2010 Feb 24;30(8):2880-7. doi: 10.1523/JNEUROSCI.4196-09.2010. J Neurosci. 2010. PMID: 20181585 Free PMC article.

8

Biochemical characterization of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctata.

Daniele A, Parenti G, d'Addio M, Andria G, Ballabio A, Meroni G. Daniele A, et al. Among authors: meroni g. Am J Hum Genet. 1998 Mar;62(3):562-72. doi: 10.1086/301746. Am J Hum Genet. 1998. PMID: 9497243 Free PMC article.

9

Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle.

Cainarca S, Messali S, Ballabio A, Meroni G. Cainarca S, et al. Among authors: meroni g. Hum Mol Genet. 1999 Aug;8(8):1387-96. doi: 10.1093/hmg/8.8.1387. Hum Mol Genet. 1999. PMID: 10400985

10

MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development.

Buchner G, Montini E, Andolfi G, Quaderi N, Cainarca S, Messali S, Bassi MT, Ballabio A, Meroni G, Franco B. Buchner G, et al. Among authors: meroni g. Hum Mol Genet. 1999 Aug;8(8):1397-407. doi: 10.1093/hmg/8.8.1397. Hum Mol Genet. 1999. PMID: 10400986

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

160 results

Search Page

Filters