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Items: 1 to 20 of 98

1.

Paragangliomas of the head and neck region show complete loss of heterozygosity at 11q22-q23 in chief cells and the flow-sorted DNA aneuploid fraction.

van Schothorst EM, Beekman M, Torremans P, Kuipers-Dijkshoorn NJ, Wessels HW, Bardoel AF, van der Mey AG, van der Vijver MJ, van Ommen GJ, Devilee P, Cornelisse CJ.

Hum Pathol. 1998 Oct;29(10):1045-9.

PMID:
9781639
3.

Allelotype of head and neck paragangliomas: allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL.

Devilee P, van Schothorst EM, Bardoel AF, Bonsing B, Kuipers-Dijkshoorn N, James MR, Fleuren G, van der Mey AG, Cornelisse CJ.

Genes Chromosomes Cancer. 1994 Oct;11(2):71-8.

PMID:
7529551
4.

Molecular pathogenesis in sporadic head and neck paraganglioma.

Bikhazi PH, Messina L, Mhatre AN, Goldstein JA, Lalwani AK.

Laryngoscope. 2000 Aug;110(8):1346-8.

PMID:
10942138
5.

Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes.

van Schothorst EM, Jansen JC, Bardoel AF, van der Mey AG, James MJ, Sobol H, Weissenbach J, van Ommen GJ, Cornelisse CJ, Devilee P.

Eur J Hum Genet. 1996;4(5):267-73.

PMID:
8946172
6.

Founder effect at PGL1 in hereditary head and neck paraganglioma families from the Netherlands.

van Schothorst EM, Jansen JC, Grooters E, Prins DE, Wiersinga JJ, van der Mey AG, van Ommen GJ, Devilee P, Cornelisse CJ.

Am J Hum Genet. 1998 Aug;63(2):468-73.

7.

Molecular genetic analysis of flow-sorted ovarian tumour cells: improved detection of loss of heterozygosity.

Abeln EC, Corver WE, Kuipers-Dijkshoorn NJ, Fleuren GJ, Cornelisse CJ.

Br J Cancer. 1994 Aug;70(2):255-62.

8.

Definition of a region of loss of heterozygosity at chromosome 11q23.3-25 in head and neck squamous cell carcinoma using laser capture microdissection technique.

Tan D, Wiseman S, Zhou Y, Li Q, Ward P, Slocum HK, Alrawi S, Loree T, Hicks W, Rigual N, Anderson G, Stoler D.

Diagn Mol Pathol. 2004 Mar;13(1):33-40.

PMID:
15163007
9.

Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases.

Riemann K, Sotlar K, Kupka S, Braun S, Zenner HP, Preyer S, Pfister M, Pusch CM, Blin N.

Cancer Genet Cytogenet. 2004 Apr 15;150(2):128-35.

PMID:
15066320
10.

Identification of a candidate tumor suppressor gene RHOBTB1 located at a novel allelic loss region 10q21 in head and neck cancer.

Beder LB, Gunduz M, Ouchida M, Gunduz E, Sakai A, Fukushima K, Nagatsuka H, Ito S, Honjo N, Nishizaki K, Shimizu K.

J Cancer Res Clin Oncol. 2006 Jan;132(1):19-27. Epub 2005 Sep 17.

PMID:
16170569
11.

Familial paragangliomas: linkage to chromosome 11q23 and clinical implications.

Milunsky J, DeStefano AL, Huang XL, Baldwin CT, Michels VV, Jako G, Milunsky A.

Am J Med Genet. 1997 Oct 3;72(1):66-70.

PMID:
9295078
12.

Familial paragangliomas: the emerging impact of molecular genetics on evaluation and management.

Bikhazi PH, Roeder E, Attaie A, Lalwani AK.

Am J Otol. 1999 Sep;20(5):639-43.

PMID:
10503587
13.

[Loss of heterozygosity on chromosome 9p13-23 in microdissected laryngeal squamous cell carcinoma by microsatellite analysis].

Xu X, An Q, Zhang J, Tang P, Cheng S.

Zhonghua Er Bi Yan Hou Ke Za Zhi. 2001 Oct;36(5):367-71. Chinese.

PMID:
12761947
14.

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.

Taschner PE, Jansen JC, Baysal BE, Bosch A, Rosenberg EH, Bröcker-Vriends AH, van Der Mey AG, van Ommen GJ, Cornelisse CJ, Devilee P.

Genes Chromosomes Cancer. 2001 Jul;31(3):274-81.

PMID:
11391798
15.
16.

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity.

Mariman EC, van Beersum SE, Cremers CW, Struycken PM, Ropers HH.

Hum Genet. 1995 Jan;95(1):56-62.

PMID:
7814027
17.

Loss of heterozygosity at 11q23 in squamous cell carcinoma of the head and neck is associated with recurrent disease.

Lazar AD, Winter MR, Nogueira CP, Larson PS, Finnemore EM, Dolan RW, Fuleihan N, Chakravarti A, Zietman A, Rosenberg CL.

Clin Cancer Res. 1998 Nov;4(11):2787-93.

18.
19.

High level of aneuploidy of chromosome 6 by FISH analysis of head and neck squamous cell carcinoma: limited applicability of LOH analysis to define HLA loss.

Koene GJ, Arts-Hilkes YH, van Dijk AJ, van der Ven KJ, Slootweg PJ, de Weger RA, Tilanus MG.

Hum Immunol. 2004 Dec;65(12):1455-62.

PMID:
15603873
20.

Identification of new minimally lost regions on 18q in head and neck squamous cell carcinoma.

Takebayashi S, Ogawa T, Jung KY, Muallem A, Mineta H, Fisher SG, Grenman R, Carey TE.

Cancer Res. 2000 Jul 1;60(13):3397-403.

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