SCOPUS 정보 검색 플랫폼

Volumn 71, Issue 1, 2001, Pages 123-126

Computational and experimental analyses reveal previously undetected coding exons of the KRIT1 (CCM1) gene

(12) Sahoo, Trilochan a Goenaga Diaz, Eduardo a Serebriiskii, Ilya G b Thomas, James W c Kotova, Elena b Cuellar, Jacob G a Peloquin, Joanna M d Golemis, Erica b Beitinjaneh, Firas e Green, Eric D c Johnson, Eric W d Marchuk, Douglas A a

a DUKE UNIVERSITY MEDICAL CENTER (United States)

b FOX CHASE CANCER CENTER (United States)

c NATIONAL HUMAN GENOME RESEARCH INSTITUTE (United States)

d BARROW NEUROLOGICAL INSTITUTE (United States)

e STONY BROOK UNIVERSITY MEDICAL CENTER (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; KRIT1 PROTEIN; RAS PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; CALCULATION; CODON; EXON; EXPRESSED SEQUENCE TAG; FRAMESHIFT MUTATION; GENE STRUCTURE; GENETIC ANALYSIS; NUCLEOTIDE SEQUENCE; PREDICTION; PRIORITY JOURNAL; START CODON;

EID: 0035145528 PISSN: 08887543 EISSN: None Source Type: Journal
DOI: 10.1006/geno.2000.6426 Document Type: Article

Times cited : (49)

References (15)

1
- 0030819029
- A physical map of human chromosome 7: An integrated YAC contig map with average STS spacing of 79 kb
- (1997) Genome Res , vol.7 , pp. 673-692
- Bouffard, G.G.¹ Idol, J.R.² Braden, V.V.³ Iyer, L.M.⁴ Cunningham, A.F.⁵ Weintraub, L.A.⁶ Touchman, J.W.⁷ Mohr-Tidwell, R.M.⁸ Peluso, D.C.⁹ Fulton, R.S.¹⁰ Ueltzen, M.S.¹¹ Weissenbach, J.¹² Magness, C.L.¹³ Green, E.D.¹⁴

2
- 0028941797
- A gene responsible for cavernous malformations of the brain maps to chromosome 7q
- (1995) Hum. Mol. Genet. , vol.4 , pp. 453-458
- Dubovsky, J.¹ Zabramski, J.M.² Kurth, J.³ Spetzler, R.F.⁴ Rich, S.S.⁵ Orr, H.T.⁶ Weber, J.L.⁷

3
- 0034702087
- KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation
- (2000) Hum. Mol. Genet. , vol.9 , Issue.9 , pp. 1351-1355
- Eerola, I.¹ Plate, K.H.² Spiegel, R.³ Boon, L.M.⁴ Mulliken, J.B.⁵ Vikkula, M.⁶

4
- 0029020926
- Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
- (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 6620-6624
- Gunel, M.¹ Awad, I.A.² Anson, J.³ Lifton, R.P.⁴

5
- 13344294378
- Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig
- (1995) Genome Res , vol.5 , pp. 368-380
- Johnson, E.W.¹ Iyer, L.M.² Rich, S.S.³ Orr, H.T.⁴ Gil-Nagel, A.⁵ Kurth, J.H.⁶ Zabramski, J.M.⁷ Marchuk, D.A.⁸ Weissenbach, J.⁹ Clericuzio, C.L.¹⁰ Davis, L.E.¹¹ Hart, B.L.¹² Gusella, J.F.¹³ Kosofsky, B.E.¹⁴ Louis, D.N.¹⁵ Morrison, L.A.¹⁶ Green, E.D.¹⁷ Weber, J.L.¹⁸

6
- 0028838285
- The natural history of cerebral cavernous malformations
- (1995) J. Neurosurg. , vol.83 , pp. 820-824
- Kondziolka, D.¹ Lunsford, L.D.² Kestle, J.R.³

7
- 0032851217
- Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas
- (1999) Nat. Genet. , vol.23 , Issue.2 , pp. 189-193
- Laberge-le Couteul, X.S.¹ Jung, H.H.² Labauge, P.³ Houtteville, J.P.⁴ Lescoat, C.⁵ Cecillon, M.⁶ Marechal, E.⁷ Joutel, A.⁸ Bach, J.F.⁹ Tournier-Lasserve, E.¹⁰

8
- 0029122978
- A locus for cerebral cavernous malformations maps to chromosome 7q in two families
- (1995) Genomics , vol.28 , pp. 311-314
- Marchuk, D.A.¹ Gallione, C.J.² Morrison, L.A.³ Clericuzio, C.L.⁴ Hart, B.L.⁵ Kosofsky, B.E.⁶ Louis, D.N.⁷ Gusella, J.F.⁸ Davis, L.E.⁹ Prenger, V.L.¹⁰

9
- 0034723456
- Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro
- (2000) DNA Res , vol.7 , pp. 65-73
- Nagase, T.¹ Kikuno, R.² Ishikawa, K.³ Hirosawa, M.⁴ Ohara, O.⁵

10
- 0023820545
- Cerebral cavernous malformations. Incidence and familial occurrence
- (1988) N. Engl. J. Med. , vol.319 , pp. 343-347
- Rigamonti, D.¹ Hadley, M.N.² Drayer, B.P.³ Johnson, P.C.⁴ Hoenig-Rigamonti, K.⁵ Knight, J.T.⁶ Spetzler, R.F.⁷

11
- 0032695959
- Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)
- (1999) Hum. Mol. Genet. , vol.8 , Issue.12 , pp. 2325-2333
- Sahoo, T.¹ Johnson, E.W.² Thomas, J.W.³ Kuehl, P.M.⁴ Jones, T.L.⁵ Dokken, C.G.⁶ Touchman, J.W.⁷ Gallione, C.J.⁸ Lee-Lin, S.Q.⁹ Kosofsky, B.¹⁰ Kurth, J.H.¹¹ Louis, D.N.¹² Mettler, G.¹³ Morrison, L.¹⁴ Gil-Nagel, A.¹⁵ Rich, S.S.¹⁶ Zabramski, J.M.¹⁷ Boguski, M.S.¹⁸ Green, E.D.¹⁹ Marchuk, D.A.²⁰ more..

12
- 0034020416
- Pip-Maker A web server for aligning two genomic DNA sequences
- (2000) Genome Res , vol.10 , Issue.4 , pp. 577-586
- Schwartz, S.¹ Zhang, Z.² Frazer, K.A.³ Smit, A.⁴ Riemer, C.⁵ Bouck, J.⁶ Gibbs, R.⁷ Hardison, R.⁸ Miller, W.⁹

13
- 0030761145
- Association of Krev-1/rap1a with KRIT1, a novel ankyrin repeat-containing protein encoded by a gene mapping to 7q21-q22
- (1997) Oncogene , vol.15 , Issue.9 , pp. 1043-1049
- Serebriiskii, I.¹ Estojak, J.² Sonoda, G.³ Testa, J.R.⁴ Golemis, E.A.⁵

14
- 0028206928
- The natural history of familial cavernous malformations: Results of an ongoing study
- (1994) J. Neurosurg. , vol.80 , pp. 422-432
- Zabramski, J.M.¹ Wascher, T.M.² Spetzler, R.F.³ Johnson, B.⁴ Golfinos, J.⁵ Drayer, B.P.⁶ Brown, B.⁷ Rigamonti, D.⁸ Brown, G.⁹

15
- 0034061825
- Mutations in KRIT1 in familial cerebral cavernous malformations
- discussion 1277-1279
- (2000) Neurosurgery , vol.46 , Issue.5 , pp. 1272-1277
- Zhang, J.¹ Clatterbuck, R.E.² Rigamonti, D.³ Dietz, H.C.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.