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Items: 1 to 20 of 112

1.

Clinical stratification of glioblastoma based on alterations in retinoblastoma tumor suppressor protein (RB1) and association with the proneural subtype.

Goldhoff P, Clarke J, Smirnov I, Berger MS, Prados MD, James CD, Perry A, Phillips JJ.

J Neuropathol Exp Neurol. 2012 Jan;71(1):83-9. doi: 10.1097/NEN.0b013e31823fe8f1.

2.

Expression and prognostic significance of TCTN1 in human glioblastoma.

Meng D, Chen Y, Zhao Y, Wang J, Yun D, Yang S, Chen J, Chen H, Lu D.

J Transl Med. 2014 Oct 11;12:288. doi: 10.1186/s12967-014-0288-9.

3.

Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis.

Kalsoom S, Wasim M, Afzal S, Shahzad MS, Ramzan S, Awan AR, Anjum AA, Ramzan K.

Mol Vis. 2015 Sep 17;21:1085-92. eCollection 2015.

4.

CDKN2/p16 or RB alterations occur in the majority of glioblastomas and are inversely correlated.

Ueki K, Ono Y, Henson JW, Efird JT, von Deimling A, Louis DN.

Cancer Res. 1996 Jan 1;56(1):150-3.

5.

Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.

Nichols KE, Houseknecht MD, Godmilow L, Bunin G, Shields C, Meadows A, Ganguly A.

Hum Mutat. 2005 Jun;25(6):566-74.

PMID:
15884040
6.

Spectrum of RB1 mutations in argentine patients: 20-years experience in the molecular diagnosis of retinoblastoma.

Ottaviani D, Parma D, Giliberto F, Ferrer M, Fandino A, Davila MT, Chantada G, Szijan I.

Ophthalmic Genet. 2013 Dec;34(4):189-98. doi: 10.3109/13816810.2012.755553. Epub 2013 Jan 10.

PMID:
23301675
7.

Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation.

Brichard B, Heusterspreute M, De Potter P, Chantrain C, Vermylen C, Sibille C, Gala JL.

Eur J Cancer. 2006 Jan;42(1):65-72.

PMID:
16343894
8.

A c.1363C>T (p.R455X) nonsense mutation of RB1 gene in a southern Chinese retinoblastoma pedigree.

Chen CY, Xu CM, Du ZF, Chen XL, Ren GL, Zhang XN.

Genet Test Mol Biomarkers. 2010 Apr;14(2):193-6. doi: 10.1089/gtmb.2009.0162.

PMID:
20059380
9.

Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.

Abidi O, Knari S, Sefri H, Charif M, Senechal A, Hamel C, Rouba H, Zaghloul K, El Kettani A, Lenaers G, Barakat A.

Mol Vis. 2011;17:3541-7. Epub 2011 Dec 30.

10.

The survival gene MED4 explains low penetrance retinoblastoma in patients with large RB1 deletion.

Dehainault C, Garancher A, Castéra L, Cassoux N, Aerts I, Doz F, Desjardins L, Lumbroso L, Montes de Oca R, Almouzni G, Stoppa-Lyonnet D, Pouponnot C, Gauthier-Villars M, Houdayer C.

Hum Mol Genet. 2014 Oct 1;23(19):5243-50. doi: 10.1093/hmg/ddu245. Epub 2014 May 23.

PMID:
24858910
11.

RB1 germ-line deletions in Argentine retinoblastoma patients.

Fernández C, Repetto K, Dalamon V, Bergonzi F, Ferreiro V, Szijan I.

Mol Diagn Ther. 2007;11(1):55-61.

PMID:
17286450
12.

Uncommon RB1 somatic mutations in a unilateral retinoblastoma patient.

Ottaviani D, Alonso C, Szijan I.

Medicina (B Aires). 2015;75(3):137-41.

13.

Short postoperative survival for glioblastoma patients with a dysfunctional Rb1 pathway in combination with no wild-type PTEN.

Bäcklund LM, Nilsson BR, Goike HM, Schmidt EE, Liu L, Ichimura K, Collins VP.

Clin Cancer Res. 2003 Sep 15;9(11):4151-8.

14.

Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma.

Amare Kadam PS, Ghule P, Jose J, Bamne M, Kurkure P, Banavali S, Sarin R, Advani S.

Cancer Genet Cytogenet. 2004 Apr 1;150(1):33-43.

PMID:
15041221
15.

MRI-localized biopsies reveal subtype-specific differences in molecular and cellular composition at the margins of glioblastoma.

Gill BJ, Pisapia DJ, Malone HR, Goldstein H, Lei L, Sonabend A, Yun J, Samanamud J, Sims JS, Banu M, Dovas A, Teich AF, Sheth SA, McKhann GM, Sisti MB, Bruce JN, Sims PA, Canoll P.

Proc Natl Acad Sci U S A. 2014 Aug 26;111(34):12550-5. doi: 10.1073/pnas.1405839111. Epub 2014 Aug 11.

16.

Loss of heterozygosity and mutations are the major mechanisms of RB1 gene inactivation in Chinese with sporadic retinoblastoma.

Choy KW, Pang CP, Yu CB, Wong HL, Ng JS, Fan DS, Lo KW, Chai JT, Wang J, Fu W, Lam DS.

Hum Mutat. 2002 Nov;20(5):408.

PMID:
12402348
17.

Unique genome-wide map of TCF4 and STAT3 targets using ChIP-seq reveals their association with new molecular subtypes of glioblastoma.

Zhang JX, Zhang J, Yan W, Wang YY, Han L, Yue X, Liu N, You YP, Jiang T, Pu PY, Kang CS.

Neuro Oncol. 2013 Mar;15(3):279-89. doi: 10.1093/neuonc/nos306. Epub 2013 Jan 7.

18.

Linkage analysis and detection of somatic, postzygous RB1 mutations in Serbian retinoblastoma patients.

Kontic M, Palacios I, Kontic M, Alonso J, Pestana A.

J BUON. 2011 Jan-Mar;16(1):142-6.

PMID:
21674866
19.

The Biology of Retinoblastoma.

Mendoza PR, Grossniklaus HE.

Prog Mol Biol Transl Sci. 2015;134:503-16. doi: 10.1016/bs.pmbts.2015.06.012. Epub 2015 Jul 14. Review.

PMID:
26310174
20.

Automated network analysis identifies core pathways in glioblastoma.

Cerami E, Demir E, Schultz N, Taylor BS, Sander C.

PLoS One. 2010 Feb 12;5(2):e8918. doi: 10.1371/journal.pone.0008918.

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