SCOPUS 정보 검색 플랫폼

Volumn 69, Issue 3, 2000, Pages 391-394

A frequent deletion polymorphism on chromosome 22q13 identified by representational difference analysis of ovarian cancer

(3) Lin, Hsingchi a Pizer, Ellen S b Morin, Patrice J a,b

a NATIONAL INSTITUTE ON AGING (United States)

b DEPARTMENT OF PATHOLOGY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; BASE MISPAIRING; CHROMOSOME 22Q; COLON CANCER; CONTROLLED STUDY; DNA SEQUENCE; EXPRESSED SEQUENCE TAG; FEMALE; GENE DELETION; GENE INSERTION; GENETIC POLYMORPHISM; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; OVARY CANCER; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

FALLOPIA;

EID: 0034331289 PISSN: 08887543 EISSN: None Source Type: Journal
DOI: 10.1006/geno.2000.6357 Document Type: Article

Times cited : (23)

References (13)

1
- 0019996193
- On the formation of spontaneous deletions: The importance of short sequence homologies in the generation of large deletions
- (1982) Cell , vol.29 , pp. 319-328
- Albertini, A.M.¹ Hofer, M.² Calos, M.P.³ Miller, J.H.⁴

2
- 0032835528
- Mapping of a target region of allelic loss to a 0.5-cM interval on chromosome 22q13 in human colorectal cancer
- (1999) Gastroenterology , vol.117 , pp. 831-837
- Castells, A.¹ Ino, Y.² Louis, D.N.³ Ramesh, V.⁴ Gusella, J.F.⁵ Rustgi, A.K.⁶

3
- 0027269573
- Human epithelial ovarian cancer allelotype
- (1993) Cancer Res. , vol.53 , pp. 2393-2398
- Cliby, W.¹ Ritland, S.² Hartmann, L.³ Dodson, M.⁴ Halling, K.C.⁵ Keeney, G.⁶ Podratz, K.C.⁷ Jenkins, R.B.⁸

4
- 0027995519
- Loss of heterozygosity on chromosome 22 in ovarian carcinoma is distal to and is not accompanied by mutations in NF2 at 22q12
- (1994) Br. J. Cancer , vol.79 , pp. 905-907
- Englefield, P.¹ Foulkes, W.D.² Campbell, I.G.³

5
- 0025182598
- Partial deletion of human alpha-galactosidase A gene in Fabry disease: Direct repeat sequences as a possible cause of slipped mispairing
- (1990) Biochem. Biophys. Res. Commun. , vol.179 , pp. 296-300
- Fukuhara, Y.¹ Sakuraba, H.² Oshima, A.³ Shimmoto, M.⁴ Nagao, Y.⁵ Nadaoka, Y.⁶ Suzuki, T.⁷ Suzuki, Y.⁸

6
- 0034100180
- Rare activation of the TCF/beta-catenin pathway in ovarian cancer
- (2000) Gynecol. Oncol. , vol.77 , pp. 97-104
- Furlong, M.T.¹ Morin, P.J.²

7
- 0027468779
- Cloning the differences between two complex genomes
- (1993) Science , vol.259 , pp. 946-951
- Lisitsyn, N.¹ Lisitsyn, N.² Wigler, M.³

8
- 0028939263
- Comparative genomic analysis of tumors: Detection of DNA losses and amplification
- (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 151-155
- Lisitsyn, N.A.¹ Lisitsina, N.M.² Dalbagni, G.³ Barker, P.⁴ Sanchez, C.A.⁵ Gnarra, J.⁶ Linehan, W.M.⁷ Reid, B.J.⁸ Wigler, M.H.⁹

9
- 0028121082
- Relationships between angiotensin I converting enzyme gene polymorphism, plasma levels, and diabetic retinal and renal complications
- (1994) Diabetes , vol.43 , pp. 384-388
- Marre, M.¹ Bernadet, P.² Gallois, Y.³ Savagner, F.⁴ Guyene, T.T.⁵ Hallab, M.⁶ Cambien, F.⁷ Passa, P.⁸ Alhenc-Gelas, F.⁹

10
- 0034037394
- An insertion/deletion polymorphism in intron 18 of the type B human natriuretic peptide receptor gene is not associated with cerebral infarction
- (2000) Hypertens. Res. , vol.23 , pp. 173-176
- Rahmutula, D.¹ Nakayama, T.² Soma, M.³ Takahashi, Y.⁴ Uwabo, J.⁵ Sato, M.⁶ Izumi, Y.⁷ Kanmatsuse, K.⁸ Ozawa, Y.⁹

11
- 0032539693
- A unified view of polymer, dumbbell, and oligonucleotide DNA nearest-neighbor thermodynamics
- (1998) Proc. Natl. Acad. Sci. USA , vol.95 , pp. 1460-1465
- SantaLucia, J.J.¹

12
- 0025796855
- Microdeletions within 22q11 associated with sporadic and familial Di-George syndrome
- (1991) Genomics , vol.10 , pp. 201-206
- Scambler, P.J.¹ Carey, A.² Wyse, R.K.³ Roach, S.⁴ Dumanski, J.P.⁵ Nordenskjold, M.⁶ Williamson, R.⁷

13
- 0030838316
- Polymorphism of the angiotensin-converting enzyme gene and cardiovascular disease
- (1997) J. Mol. Med. , vol.75 , pp. 867-875
- Schunkert, H.¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.