Gentile M - Search Results

1

Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defects.

Gentile M, Ranieri C, Loconte DC, Ponzi E, Ficarella R, Volpe P, Scalzo G, Lepore Signorile M, Grossi V, Cordella A, Ventola GM, Susca FC, Turchiano A, Simone C, Resta N. Gentile M, et al. Clin Genet. 2021 Mar;99(3):425-429. doi: 10.1111/cge.13890. Epub 2020 Nov 30. Clin Genet. 2021. PMID: 33236357

2

Familial adenomatous polyposis: identification of a new frameshift mutation of the APC gene in an Italian family.

Stella A, Lonoce A, Resta N, Gentile M, Susca F, Mareni C, Brescia G, Origoni P, Montero MP, Guanti G. Stella A, et al. Among authors: gentile m. Biochem Biophys Res Commun. 1992 May 15;184(3):1357-63. doi: 10.1016/s0006-291x(05)80032-4. Biochem Biophys Res Commun. 1992. PMID: 1350438

3

Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients.

Stella A, Montera M, Resta N, Marchese C, Susca F, Gentile M, Romio L, Pilia S, Prete F, Mareni C, et al. Stella A, et al. Among authors: gentile m. Hum Mol Genet. 1994 Sep;3(9):1687-8. doi: 10.1093/hmg/3.9.1687. Hum Mol Genet. 1994. PMID: 7833931 No abstract available.

4

Linkage studies in Italian families with familial adenomatous polyposis.

Mareni C, Stella A, Origone P, Susca F, Montera MP, Lonoce A, Ponz de Leon M, Sassatelli R, Gentile M, Straface A, et al. Mareni C, et al. Among authors: gentile m. Hum Genet. 1993 Jan;90(5):545-50. doi: 10.1007/BF00217456. Hum Genet. 1993. PMID: 8094067

5

Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP).

Stella A, Resta N, Gentile M, Susca F, Mareni C, Montera MP, Guanti G. Stella A, et al. Among authors: gentile m. Am J Hum Genet. 1993 Nov;53(5):1031-7. Am J Hum Genet. 1993. PMID: 8213830 Free PMC article.

6

Infertility in carriers of two bisatellited marker chromosomes.

Gentile M, Susca F, Resta N, Stella A, Cascone A, Guanti G. Gentile M, et al. Clin Genet. 1993 Aug;44(2):71-5. doi: 10.1111/j.1399-0004.1993.tb03849.x. Clin Genet. 1993. PMID: 8275562

7

An unusual dicentric Y chromosome with a functional centromere with no detectable alpha-satellite.

Bukvic N, Susca F, Gentile M, Tangari E, Ianniruberto A, Guanti G. Bukvic N, et al. Among authors: gentile m. Hum Genet. 1996 Apr;97(4):453-6. doi: 10.1007/BF02267065. Hum Genet. 1996. PMID: 8834241

8

COACH syndrome: report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation.

Gentile M, Di Carlo A, Susca F, Gambotto A, Caruso ML, Panella C, Vajro P, Guanti G. Gentile M, et al. Am J Med Genet. 1996 Aug 23;64(3):514-20. doi: 10.1002/(SICI)1096-8628(19960823)64:3<514::AID-AJMG13>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8862632

9

The familial adenomatous polyposis region exhibits many different haplotypes.

Stella A, Resta N, Polizzi A, Montera M, Cariola F, Susca F, Gismondi V, Bertario L, Marchese C, Tenconi R, Tibiletti MG, Izzo P, Gentile M, Prete F, Pannarale O, Di Matteo G, Sala P, Varesco L, Mareni C, Guanti G. Stella A, et al. Among authors: gentile m. Hum Genet. 1998 Jun;102(6):624-8. doi: 10.1007/s004390050752. Hum Genet. 1998. PMID: 9703421

10

STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer.

Resta N, Simone C, Mareni C, Montera M, Gentile M, Susca F, Gristina R, Pozzi S, Bertario L, Bufo P, Carlomagno N, Ingrosso M, Rossini FP, Tenconi R, Guanti G. Resta N, et al. Among authors: gentile m. Cancer Res. 1998 Nov 1;58(21):4799-801. Cancer Res. 1998. PMID: 9809980

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