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Items: 1 to 20 of 178

1.

Analysis of chromosome 9p21 deletion and p16 gene mutation in salivary gland carcinomas.

Cerilli LA, Swartzbaugh JR, Saadut R, Marshall CE, Rumpel CA, Moskaluk CA, Frierson HF Jr.

Hum Pathol. 1999 Oct;30(10):1242-6.

PMID:
10534174
2.

Alterations of p16-pRb pathway and chromosome locus 9p21-22 in sporadic invasive breast carcinomas.

Gorgoulis VG, Koutroumbi EN, Kotsinas A, Zacharatos P, Markopoulos C, Giannikos L, Kyriakou V, Voulgaris Z, Gogas I, Kittas C.

Mol Med. 1998 Dec;4(12):807-22.

3.

Loss of heterozygosity on chromosome 6q correlates with decreased thrombospondin-2 expression in human salivary gland carcinomas.

Kishi M, Nakamura M, Nishimine M, Ishida E, Shimada K, Kirita T, Konishi N.

Cancer Sci. 2003 Jun;94(6):530-5.

4.

Somatic INK4a-ARF locus mutations: a significant mechanism of gene inactivation in squamous cell carcinomas of the head and neck.

Poi MJ, Yen T, Li J, Song H, Lang JC, Schuller DE, Pearl DK, Casto BC, Tsai MD, Weghorst CM.

Mol Carcinog. 2001 Jan;30(1):26-36.

PMID:
11255261
5.

Homozygous deletions at chromosome 9p21 and mutation analysis of p16 and p15 in microdissected primary non-small cell lung cancers.

Packenham JP, Taylor JA, White CM, Anna CH, Barrett JC, Devereux TR.

Clin Cancer Res. 1995 Jul;1(7):687-90.

6.

Definition of three minimal deleted regions by comprehensive allelotyping and mutational screening of FHIT,p16(INK4A), and p19(ARF) genes in nasopharyngeal carcinoma.

Ko JY, Lee TC, Hsiao CF, Lin GL, Yen SH, Chen KY, Hsiung CA, Chen PJ, Hsu MM, Jou YS.

Cancer. 2002 Apr 1;94(7):1987-96.

7.

Hybrid carcinomas of the salivary glands: report of nine cases with a clinicopathologic, immunohistochemical, and p53 gene alteration analysis.

Nagao T, Sugano I, Ishida Y, Asoh A, Munakata S, Yamazaki K, Konno A, Iwaya K, Shimizu T, Serizawa H, Ebihara Y.

Mod Pathol. 2002 Jul;15(7):724-33.

8.
9.

Loss of heterozygosity and mutation analysis of the p16 (9p21) and p53 (17p13) genes in squamous cell carcinoma of the head and neck.

González MV, Pello MF, López-Larrea C, Suárez C, Menéndez MJ, Coto E.

Clin Cancer Res. 1995 Sep;1(9):1043-9.

10.

p16MTS1/CDK4I mutations and concomitant loss of heterozygosity at 9p21-23 are frequent events in squamous cell carcinoma of the larynx.

Jares P, Fernández PL, Nadal A, Cazorla M, Hernández L, Pinyol M, Hernández S, Traserra J, Cardesa A, Campo E.

Oncogene. 1997 Sep 18;15(12):1445-53.

11.

[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
12.

Loss of heterozygosity at chromosome 9p21 is a frequent finding in enteropathy-type T-cell lymphoma.

Obermann EC, Diss TC, Hamoudi RA, Munson P, Wilkins BS, Camozzi ML, Isaacson PG, Du MQ, Dogan A.

J Pathol. 2004 Feb;202(2):252-62.

PMID:
14743509
13.

Frequency of mutation and deletion of the tumor suppressor gene CDKN2A (MTS1/p16) in hepatocellular carcinoma from an Australian population.

Biden K, Young J, Buttenshaw R, Searle J, Cooksley G, Xu DB, Leggett B.

Hepatology. 1997 Mar;25(3):593-7.

PMID:
9049204
14.

Alterations of p16(INK4a) and p14(ARF) in patients with severe oral epithelial dysplasia.

Kresty LA, Mallery SR, Knobloch TJ, Song H, Lloyd M, Casto BC, Weghorst CM.

Cancer Res. 2002 Sep 15;62(18):5295-300.

15.

Chromosome 6 deletion and candidate tumor suppressor genes in adenoid cystic carcinoma.

Rutherford S, Yu Y, Rumpel CA, Frierson HF Jr, Moskaluk CA.

Cancer Lett. 2006 May 18;236(2):309-17.

PMID:
16054751
17.

9p21 deletion correlates with recurrence in head and neck cancer.

Lydiatt WM, Davidson BJ, Schantz SP, Caruana S, Chaganti RS.

Head Neck. 1998 Mar;20(2):113-8.

PMID:
9484941
18.

Analysis of p16 (CDKN2/MTS-1/INK4A) alterations in primary sporadic uveal melanoma.

Merbs SL, Sidransky D.

Invest Ophthalmol Vis Sci. 1999 Mar;40(3):779-83.

PMID:
10067984
19.

Homozygous deletions at chromosome 9p21 involving p16 and p15 are associated with histologic progression in follicle center lymphoma.

Elenitoba-Johnson KS, Gascoyne RD, Lim MS, Chhanabai M, Jaffe ES, Raffeld M.

Blood. 1998 Jun 15;91(12):4677-85.

20.

INK4a-ARF alterations and p53 mutations in primary and consecutive squamous cell carcinoma of the head and neck.

Weber A, Bellmann U, Bootz F, Wittekind C, Tannapfel A.

Virchows Arch. 2002 Aug;441(2):133-42.

PMID:
12189502

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