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Items: 20

1.

Design and synthesis of 2-oxindole based multi-targeted inhibitors of PDK1/Akt signaling pathway for the treatment of glioblastoma multiforme.

Sestito S, Nesi G, Daniele S, Martelli A, Digiacomo M, Borghini A, Pietra D, Calderone V, Lapucci A, Falasca M, Parrella P, Notarangelo A, Breschi MC, Macchia M, Martini C, Rapposelli S.

Eur J Med Chem. 2015 Nov 13;105:274-88. doi: 10.1016/j.ejmech.2015.10.020. Epub 2015 Oct 22.

PMID:
26498573
2.

Translocation of the proto-oncogene Bcl-6 in human glioblastoma multiforme.

Ruggieri S, Tamma R, Marzullo A, Annese T, Marinaccio C, Errede M, Susca FC, Senetta R, Cassoni P, Vacca A, Albano F, Saracino C, Notarangelo A, Specchia G, Ribatti D, Nico B.

Cancer Lett. 2014 Oct 10;353(1):41-51. doi: 10.1016/j.canlet.2014.06.017. Epub 2014 Jul 17.

3.

Establishment and genetic characterization of ANGM-CSS, a novel, immortal cell line derived from a human glioblastoma multiforme.

Notarangelo A, Trombetta D, D'Angelo V, Parrella P, Palumbo O, Storlazzi CT, Impera L, Muscarella LA, La Torre A, Affuso A, Fazio VM, Carella M, Zelante L.

Int J Oncol. 2014 Mar;44(3):717-24. doi: 10.3892/ijo.2013.2224. Epub 2013 Dec 23.

PMID:
24366606
4.

Sedlin controls the ER export of procollagen by regulating the Sar1 cycle.

Venditti R, Scanu T, Santoro M, Di Tullio G, Spaar A, Gaibisso R, Beznoussenko GV, Mironov AA, Mironov A Jr, Zelante L, Piemontese MR, Notarangelo A, Malhotra V, Vertel BM, Wilson C, De Matteis MA.

Science. 2012 Sep 28;337(6102):1668-72.

5.

[Counseling on life style delivered during cancer secondary prevention practice: considerations after the SPRINT study experience in Florence, Mantua and Turin].

Grechi E, Chellini E, Bellati C; Gruppo di lavoro SPRINT.

Epidemiol Prev. 2012 Jan;36(1):56-8. Italian.

PMID:
22418804
6.

Regulation of KEAP1 expression by promoter methylation in malignant gliomas and association with patient's outcome.

Muscarella LA, Barbano R, D'Angelo V, Copetti M, Coco M, Balsamo T, la Torre A, Notarangelo A, Troiano M, Parisi S, Icolaro N, Catapano D, Valori VM, Pellegrini F, Merla G, Carella M, Fazio VM, Parrella P.

Epigenetics. 2011 Mar;6(3):317-25. Epub 2011 Mar 1.

7.

Calcium-sensing receptor (CASR) mutations in hypercalcemic states: studies from a single endocrine clinic over three years.

Guarnieri V, Canaff L, Yun FH, Scillitani A, Battista C, Muscarella LA, Wong BY, Notarangelo A, D'Agruma L, Sacco M, Cole DE, Hendy GN.

J Clin Endocrinol Metab. 2010 Apr;95(4):1819-29. doi: 10.1210/jc.2008-2430. Epub 2010 Feb 17.

PMID:
20164288
8.

High specificity of quantitative methylation-specific PCR analysis for MGMT promoter hypermethylation detection in gliomas.

Parrella P, la Torre A, Copetti M, Valori VM, Barbano R, Notarangelo A, Bisceglia M, Gallo AP, Balsamo T, Poeta ML, Carella M, Catapano D, Parisi S, Dallapiccola B, Maiello E, D'Angelo V, Fazio VM.

J Biomed Biotechnol. 2009;2009:531692. doi: 10.1155/2009/531692. Epub 2009 Jun 1.

9.

Homocysteine levels in amniotic fluid. Relationship with birth-weight.

Grandone E, Colaizzo D, Vecchione G, Sciannamè N, Notarangelo A, Croce AI, Margaglione M.

Thromb Haemost. 2006 Apr;95(4):625-8.

PMID:
16601832
10.

Interstitial "de novo" tandem duplication of 7(q31.1-q35): first reported case.

Zelante L, Croce AI, Grifa A, Notarangelo A, Calvano S.

Ann Genet. 2003 Jan-Mar;46(1):49-52.

PMID:
12818530
11.

A complex mosaicism 45,X/46,X,del(Xq)/46,X,idic(Xq) in a patient with secondary amenorrhea.

Calvano S, de Cillis GP, Croce AI, Perla G, Notarangelo A, Zelante L.

Ann Genet. 2002 Jul-Sep;45(3):137-40.

PMID:
12381444
12.

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.

Melchionda S, Ahituv N, Bisceglia L, Sobe T, Glaser F, Rabionet R, Arbones ML, Notarangelo A, Di Iorio E, Carella M, Zelante L, Estivill X, Avraham KB, Gasparini P.

Am J Hum Genet. 2001 Sep;69(3):635-40. Epub 2001 Jul 20.

13.

Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions.

Centra M, Memeo E, d'Apolito M, Savino M, Ianzano L, Notarangelo A, Liu J, Doggett NA, Zelante L, Savoia A.

Genomics. 1998 Aug 1;51(3):463-7.

PMID:
9721219
14.

Positional cloning of the Fanconi anaemia group A gene.

Fanconi anaemia/Breast cancer consortium.

Nat Genet. 1996 Nov;14(3):324-8.

PMID:
8896564
15.

Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity.

Gasparini P, Calonge MJ, Bisceglia L, Purroy J, Dianzani I, Notarangelo A, Rousaud F, Gallucci M, Testar X, Ponzone A, et al.

Am J Hum Genet. 1995 Oct;57(4):781-8.

16.

The 18ph+ chromosome heteromorphism.

Zelante L, Notarangelo A, Dallapiccola B.

Prenat Diagn. 1994 Nov;14(11):1096-7. No abstract available.

PMID:
7877960
17.

Cytogenetic and molecular analysis of trisomy 9. Case report and review.

Zelante L, Notarangelo A, Croce AI, Piemontese MR, Gasparini P.

Ann Genet. 1994;37(1):21-5.

PMID:
8010708
18.

On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndrome.

Martini G, Carillo G, Catizone F, Notarangelo A, Mingarelli R, Dallapiccola B.

Prenat Diagn. 1993 Aug;13(8):763-6.

PMID:
8284294
19.

The parental origin of hydatidiform moles and blighted ova: molecular probing with hypervariable DNA polymorphisms.

Trabetti E, Galavotti R, Zanini L, Zardini E, Zatti N, Bernardi F, Notarangelo A, Croce AI, Pignatti PF, Gasparini P.

Mol Cell Probes. 1993 Aug;7(4):325-9.

PMID:
8232349
20.

Ring chromosome 21 in healthy persons: different consequences in females and in males.

Dallapiccola B, De Filippis V, Notarangelo A, Perla G, Zelante L.

Hum Genet. 1986 Jul;73(3):218-20.

PMID:
3733078

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