Pizzuti A - Search Results

1

Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster.

Ratti A, Amati F, Bozzali M, Conti E, Sangiuolo F, Berloco M, Palumbo G, Botta A, Pizzuti A, Novelli G, Dallapiccola B. Ratti A, et al. Among authors: pizzuti a. Cytogenet Cell Genet. 2001;92(3-4):279-82. doi: 10.1159/000056916. Cytogenet Cell Genet. 2001. PMID: 11435701

2

Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.

Pizzuti A, Novelli G, Mari A, Ratti A, Colosimo A, Amati F, Penso D, Sangiuolo F, Calabrese G, Palka G, Silani V, Gennarelli M, Mingarelli R, Scarlato G, Scambler P, Dallapiccola B. Pizzuti A, et al. Am J Hum Genet. 1996 Apr;58(4):722-9. Am J Hum Genet. 1996. PMID: 8644734 Free PMC article.

3

cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene.

Pizzuti A, Amati F, Calabrese G, Mari A, Colosimo A, Silani V, Giardino L, Ratti A, Penso D, Calzà L, Palka G, Scarlato G, Novelli G, Dallapiccola B. Pizzuti A, et al. Hum Mol Genet. 1996 Jul;5(7):953-8. doi: 10.1093/hmg/5.7.953. Hum Mol Genet. 1996. PMID: 8817329

4

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome.

Pizzuti A, Novelli G, Ratti A, Amati F, Mari A, Calabrese G, Nicolis S, Silani V, Marino B, Scarlato G, Ottolenghi S, Dallapiccola B. Pizzuti A, et al. Hum Mol Genet. 1997 Feb;6(2):259-65. doi: 10.1093/hmg/6.2.259. Hum Mol Genet. 1997. PMID: 9063746

5

Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 gene.

Botta A, Jurecic V, Pizzuti A, Novelli G, Dallapiccola B, Baldini A. Botta A, et al. Among authors: pizzuti a. Cytogenet Cell Genet. 1997;77(3-4):264-5. doi: 10.1159/000134592. Cytogenet Cell Genet. 1997. PMID: 9284932 No abstract available.

6

Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L).

Novelli G, Mari A, Amati F, Colosimo A, Sangiuolo F, Bengala M, Conti E, Ratti A, Bordoni R, Pizzuti A, Baldini A, Crinelli R, Pandolfi F, Magnani M, Dallapiccola B. Novelli G, et al. Among authors: pizzuti a. Biochim Biophys Acta. 1998 Mar 9;1396(2):158-62. doi: 10.1016/s0167-4781(97)00211-x. Biochim Biophys Acta. 1998. PMID: 9540831

7

Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome.

Pizzuti A, Novelli G, Ratti A, Amati F, Bordoni R, Mandich P, Bellone E, Conti E, Bengala M, Mari A, Silani V, Dallapiccola B. Pizzuti A, et al. Mol Genet Metab. 1999 Jul;67(3):227-35. doi: 10.1006/mgme.1999.2868. Mol Genet Metab. 1999. PMID: 10381330

8

Characterization of a new TSPY gene family member in Yq (TSPYq1).

Ratti A, Stuppia L, Gatta V, Fogh I, Calabrese G, Pizzuti A, Palka G. Ratti A, et al. Among authors: pizzuti a. Cytogenet Cell Genet. 2000;88(1-2):159-62. doi: 10.1159/000015510. Cytogenet Cell Genet. 2000. PMID: 10773691

9

Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene.

Digilio MC, Conti E, Sarkozy A, Mingarelli R, Dottorini T, Marino B, Pizzuti A, Dallapiccola B. Digilio MC, et al. Among authors: pizzuti a. Am J Hum Genet. 2002 Aug;71(2):389-94. doi: 10.1086/341528. Epub 2002 Jun 7. Am J Hum Genet. 2002. PMID: 12058348 Free PMC article.

10

Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.

Wadey R, McKie J, Papapetrou C, Sutherland H, Lohman F, Osinga J, Frohn I, Hofstra R, Meijers C, Amati F, Conti E, Pizzuti A, Dallapiccola B, Novelli G, Scambler P. Wadey R, et al. Among authors: pizzuti a. Am J Hum Genet. 1999 Jul;65(1):247-9. doi: 10.1086/302468. Am J Hum Genet. 1999. PMID: 10364538 Free PMC article. No abstract available.

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