SCOPUS 정보 검색 플랫폼

Volumn 59, Issue 2, 1996, Pages 400-406

Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions

(9) Henske, Elizabeth Petri a,h Scheithauer, Bernd W b Short, M Priscilla c Wollmann, Robert c Nahmias, Joseph d Hornigold, Nick e Van Slegtenhorst, Marjon f Welsh, Cynthia T g Kwiatkowski, David J a

a BRIGHAM AND WOMEN S HOSPITAL (United States)

b MAYO CLINIC (United States)

c UNIVERSITY OF CHICAGO (United States)

d MEDICAL RESEARCH COUNCIL (United Kingdom)

e UNIVERSITY COLLEGE LONDON (United Kingdom)

f ERASMUS UNIVERSITY ROTTERDAM (Netherlands)

g UNIVERSITY OF UTAH SCHOOL OF MEDICINE (United States)

h FOX CHASE CANCER CENTER (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN TUMOR; CHROMOSOME 16P; CHROMOSOME 9Q; CHROMOSOME MAP; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DNA DETERMINATION; GENE LOSS; HEART TUMOR; HETEROZYGOSITY; HUMAN; HUMAN TISSUE; KIDNEY TUMOR; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TUBEROUS SCLEROSIS; TUMOR SUPPRESSOR GENE;

ALLELES; ANGIOMYOLIPOMA; BASE SEQUENCE; BRAIN; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 9; HETEROZYGOTE; HUMANS; KIDNEY; MOLECULAR SEQUENCE DATA; RHABDOMYOMA; TUBEROUS SCLEROSIS;

EID: 0029831886 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (300)

References (3)

1
- 0027992456
- 9q34 loss of heterozygosity in a tuberous sclerosis astrocytoma suggests a growth suppressor-like activity also for the TSC1 gene
- Carbonara C, Longa L, Grosso E, Borrone C, Garre MG, Brisigotti M and Bigone N (1994) 9q34 loss of heterozygosity in a tuberous sclerosis astrocytoma suggests a growth suppressor-like activity also for the TSC1 gene. Hum Mol Genet 3:1829-1832
- (1994) Hum Mol Genet , vol.3 , pp. 1829-1832
- Carbonara, C.¹ Longa, L.² Grosso, E.³ Borrone, C.⁴ Garre, M.G.⁵ Brisigotti, M.⁶ Bigone, N.⁷

2
- 9044220611
- Apparent preferential loss of heterozygosity at TSC2 over TSC1 chromosomal region in tuberous sclerosis hamartomas
- Carbonara C, Longa L, Grosso E, Mazzuco G, Borrone C, Garre ML, Brisigotti M, et al (1996) Apparent preferential loss of heterozygosity at TSC2 over TSC1 chromosomal region in tuberous sclerosis hamartomas. Genes Chromosom Cancer 15:18-25
- (1996) Genes Chromosom Cancer , vol.15 , pp. 18-25
- Carbonara, C.¹ Longa, L.² Grosso, E.³ Mazzuco, G.⁴ Borrone, C.⁵ Garre, M.L.⁶ Brisigotti, M.⁷

3
- 0029160585
- Benign neurofibromas in type l neurofibromatosis (NF1) show somatic deletions of the NF1 gene
- Colman SD, Williams CA and Wallace MR (1995) Benign neurofibromas in type l neurofibromatosis (NF1) show somatic deletions of the NF1 gene. Nat Genet 11:90-92
- (1995) Nat Genet , vol.11 , pp. 90-92
- Colman, S.D.¹ Williams, C.A.² Wallace, M.R.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.