SCOPUS 정보 검색 플랫폼

PLoS Medicine

Volumn 3, Issue 3, 2006, Pages 413-414

Mitochondria: More than mitochondrial DNA in cancer [5]

(1) Baysal, Bora a

a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

CARCINOGENESIS; CHROMOSOME BAND; FAMILIAL CANCER; GENE MUTATION; LETTER; MITOCHONDRION; MOLECULAR CLONING; PARAGANGLIOMA; PHEOCHROMOCYTOMA; GENETIC VARIABILITY; GENETICS; HUMAN; NEOPLASM; NOTE; PATHOLOGY;

DNA, MITOCHONDRIAL; GENETIC VARIATION; HUMANS; MITOCHONDRIA; NEOPLASMS;

EID: 33645375947 PISSN: 15491277 EISSN: 15491676 Source Type: Journal
DOI: 10.1371/journal.pmed.0030156 Document Type: Letter

Times cited : (5)

References (4)

1
- 28444447123
- A critical reassessment of the role of mitochondria in tumorigenesis
- DOI: 10.1371/journal.pmed.0020296
- Salas A, Yao YG, Macaulay V, Vega A, Carracedo A, et al. (2005) A critical reassessment of the role of mitochondria in tumorigenesis. PLoS Med 2: e296. DOI: 10.1371/journal.pmed.0020296
- (2005) PLoS Med , vol.2
- Salas, A.¹ Yao, Y.G.² Macaulay, V.³ Vega, A.⁴ Carracedo, A.⁵

2
- 0034602950
- Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
- Baysal BE, Ferrell RE, Willett-Brozick JE, Lawrence EC, Myssiorek D, et al. (2000) Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 287: 848-851.
- (2000) Science , vol.287 , pp. 848-851
- Baysal, B.E.¹ Ferrell, R.E.² Willett-Brozick, J.E.³ Lawrence, E.C.⁴ Myssiorek, D.⁵

3
- 29144484161
- The SDH mutation database: An online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency
- Bayley JP, Devilee P, Taschner PE (2005) The SDH mutation database: An online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency. BMC Med Genet 6: 39.
- (2005) BMC Med Genet , vol.6 , pp. 39
- Bayley, J.P.¹ Devilee, P.² Taschner, P.E.³

4
- 18544365990
- Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer
- Tomlinson IP, Alam NA, Rowan AJ, Barclay E, Jaeger EE, et al. (2002) Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. Nat Genet 30: 406-410.
- (2002) Nat Genet , vol.30 , pp. 406-410
- Tomlinson, I.P.¹ Alam, N.A.² Rowan, A.J.³ Barclay, E.⁴ Jaeger, E.E.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.