Gennarelli M - Search Results

1

Genomic instability associated with myotonic dystrophy does not involve p53 expression and activity.

Gennarelli M, Lucarelli M, Amicucci P, Soddu S, Novelli G, Dallapiccola B. Gennarelli M, et al. Cell Biochem Funct. 1998 Jun;16(2):117-22. doi: 10.1002/(SICI)1099-0844(199806)16:2<117::AID-CBF776>3.0.CO;2-X. Cell Biochem Funct. 1998. PMID: 9636999

2

Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscle.

Novelli G, Gennarelli M, Zelano G, Sangiuolo F, Lo Cicero S, Samson F, Dallapiccola B. Novelli G, et al. Among authors: gennarelli m. Cell Biochem Funct. 1992 Dec;10(4):251-6. doi: 10.1002/cbf.290100407. Cell Biochem Funct. 1992. PMID: 1473264

3

Discordant clinical outcome in myotonic dystrophy relatives showing (CTG)n > 700 repeats.

Novelli G, Gennarelli M, Menegazzo E, Angelini C, Dallapiccola B. Novelli G, et al. Among authors: gennarelli m. Neuromuscul Disord. 1995 Mar;5(2):157-9. doi: 10.1016/0960-8966(94)00044-a. Neuromuscul Disord. 1995. PMID: 7767095

4

Failure in detecting mRNA transcripts from the mutated allele in myotonic dystrophy muscle.

Novelli G, Gennarelli M, Zelano G, Pizzuti A, Fattorini C, Caskey CT, Dallapiccola B. Novelli G, et al. Among authors: gennarelli m. Biochem Mol Biol Int. 1993 Feb;29(2):291-7. Biochem Mol Biol Int. 1993. PMID: 8495213

5

Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats.

Gennarelli M, Novelli G, Andreasi Bassi F, Martorell L, Cornet M, Menegazzo E, Mostacciuolo ML, Martinez JM, Angelini C, Pizzuti A, Baiget M, Dallapiccola B. Gennarelli M, et al. Am J Med Genet. 1996 Nov 11;65(4):342-7. doi: 10.1002/(SICI)1096-8628(19961111)65:4<342::AID-AJMG18>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8923947

6

A single polymerase chain reaction-based protocol for detecting normal and expanded alleles in myotonic dystrophy.

Gennarelli M, Pavoni M, Amicucci P, Novelli G, Dallapiccola B. Gennarelli M, et al. Diagn Mol Pathol. 1998 Jun;7(3):135-7. doi: 10.1097/00019606-199806000-00002. Diagn Mol Pathol. 1998. PMID: 9836067

7

Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients.

Gennarelli M, Pavoni M, Amicucci P, Angelini C, Menegazzo E, Zelano G, Novelli G, Dallapiccola B. Gennarelli M, et al. Neuromuscul Disord. 1999 Jun;9(4):215-9. doi: 10.1016/s0960-8966(99)00003-6. Neuromuscul Disord. 1999. PMID: 10399747

8

CTG repeats distribution and Alu insertion polymorphism at myotonic dystrophy (DM) gene in Amhara and Oromo populations of Ethiopia.

Gennarelli M, Pavoni M, Cruciani F, De Stefano G, Dallapiccola B, Novelli G. Gennarelli M, et al. Hum Genet. 1999 Jul-Aug;105(1-2):165-7. doi: 10.1007/s004399900091. Hum Genet. 1999. PMID: 10480373

9

Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma.

Amicucci P, Gennarelli M, Novelli G, Dallapiccola B. Amicucci P, et al. Among authors: gennarelli m. Clin Chem. 2000 Feb;46(2):301-2. Clin Chem. 2000. PMID: 10657396 Clinical Trial. No abstract available.

10

Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients.

Salehi LB, Bonifazi E, Stasio ED, Gennarelli M, Botta A, Vallo L, Iraci R, Massa R, Antonini G, Angelini C, Novelli G. Salehi LB, et al. Among authors: gennarelli m. Genet Test. 2007 Spring;11(1):84-90. doi: 10.1089/gte.2006.0511. Genet Test. 2007. PMID: 17394397

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