Puliti A - Search Results

1

Deleted and normal chromosome 10 homologs from a patient with Hirschsprung disease isolated in two cell hybrids through enrichment by immunomagnetic selection.

Puliti A, Covone AE, Bicocchi MP, Bolino A, Lerone M, Martucciello G, Jasonni V, Romeo G. Puliti A, et al. Cytogenet Cell Genet. 1993;63(2):102-6. doi: 10.1159/000133510. Cytogenet Cell Genet. 1993. PMID: 8467706

2

Assignment of mouse Gfra1, the homologue of a new human HSCR candidate gene, to the telomeric region of mouse chromosome 19.

Puliti A, Cinti R, Seri M, Ceccherini I, Romeo G. Puliti A, et al. Cytogenet Cell Genet. 1997;78(3-4):291-4. doi: 10.1159/000134675. Cytogenet Cell Genet. 1997. PMID: 9465906

3

HOX11L1, a gene involved in peripheral nervous system development, maps to human chromosome 2p13.1-->p12 and mouse chromosome 6C3-D1.

Puliti A, Cinti R, Betsos N, Romeo G, Ceccherini I. Puliti A, et al. Cytogenet Cell Genet. 1999;84(1-2):115-7. doi: 10.1159/000015234. Cytogenet Cell Genet. 1999. PMID: 10343123

4

A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10.

Lyonnet S, Bolino A, Pelet A, Abel L, Nihoul-Fékété C, Briard ML, Mok-Siu V, Kaariainen H, Martucciello G, Lerone M, Puliti A, Luo Y, Weissenbach J, Devoto M, Munnich A, Romeo G. Lyonnet S, et al. Among authors: puliti a. Nat Genet. 1993 Aug;4(4):346-50. doi: 10.1038/ng0893-346. Nat Genet. 1993. PMID: 8401580

5

Preliminary results on the frequency of the delta F508 mutation in cystic fibrosis patients from the USSR.

Ronchetto P, Devoto M, Puliti A, Romeo G, Sokolov B, Kalinin VN, Vorsanova SG, Krainiaia GV, Reznik BY. Ronchetto P, et al. Among authors: puliti a. Hum Genet. 1990 Sep;85(4):423-4. doi: 10.1007/BF02428294. Hum Genet. 1990. PMID: 2210759

6

Sequence and characterisation of the RET proto-oncogene 5' flanking region: analysis of retinoic acid responsiveness at the transcriptional level.

Patrone G, Puliti A, Bocciardi R, Ravazzolo R, Romeo G. Patrone G, et al. Among authors: puliti a. FEBS Lett. 1997 Dec 8;419(1):76-82. doi: 10.1016/s0014-5793(97)01435-x. FEBS Lett. 1997. PMID: 9426223 Free article.

7

Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion.

Tassano E, Mirabelli-Badenier M, Veneselli E, Puliti A, Lerone M, Vaccari CM, Morana G, Porta S, Gimelli G, Cuoco C. Tassano E, et al. Among authors: puliti a. Mol Cytogenet. 2015 Apr 28;8:31. doi: 10.1186/s13039-015-0134-7. eCollection 2015. Mol Cytogenet. 2015. PMID: 26052347 Free PMC article.

8

Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a low-frequency noncoding RBM8A SNP: a new familial case.

Tassano E, Gimelli S, Divizia MT, Lerone M, Vaccari C, Puliti A, Gimelli G. Tassano E, et al. Among authors: puliti a. Mol Cytogenet. 2015 Nov 5;8:87. doi: 10.1186/s13039-015-0188-6. eCollection 2015. Mol Cytogenet. 2015. PMID: 26550033 Free PMC article.

9

Genomic organisation of the mouse Ret proto-oncogene.

Panetta D, Yin L, Barale R, Romeo G, Ravazzolo R, Ceccherini I, Puliti A. Panetta D, et al. Among authors: puliti a. DNA Seq. 2001;11(6):501-6. doi: 10.3109/10425170109041333. DNA Seq. 2001. PMID: 11696976

10

Assessment of copy number variations in 120 patients with Poland syndrome.

Vaccari CM, Tassano E, Torre M, Gimelli S, Divizia MT, Romanini MV, Bossi S, Musante I, Valle M, Senes F, Catena N, Bedeschi MF, Baban A, Calevo MG, Acquaviva M, Lerone M, Ravazzolo R, Puliti A. Vaccari CM, et al. Among authors: puliti a. BMC Med Genet. 2016 Nov 25;17(1):89. doi: 10.1186/s12881-016-0351-x. BMC Med Genet. 2016. PMID: 27884122 Free PMC article.

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