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Volumn 160, Issue 4, 2002, Pages 1541-1542

Beckwith- wiedemann syndrome, pancreatoblastoma, and the wnt signaling pathway [1] (multiple letters)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SUBSTITUTION; AMINO TERMINAL SEQUENCE; BECKWITH WIEDEMANN SYNDROME; CARCINOGENESIS; CASE REPORT; CHROMOSOME 11P; CLINICAL FEATURE; EXON; GENE DELETION; GENE MUTATION; GENE SEQUENCE; GENETIC SCREENING; HEMIHYPERTROPHY; HEPATOBLASTOMA; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; LETTER; MALE; NEPHROBLASTOMA; PANCREAS TUMOR; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; SEQUENCE ANALYSIS; SIGNAL TRANSDUCTION;

EID: 0036105787     PISSN: 00029440     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9440(10)62580-1     Document Type: Letter
Times cited : (18)

References (11)
  • 1
    • 0035152551 scopus 로고    scopus 로고
    • Distinctive genetic alterations in sporadic and familial adenomatous polyposis-associated pancreatoblastomas: frequent alterations in the APC/β-catenin pathway and chromosome 11p
    • SC Abraham TT Wu DS Klimstra LS Finn JH Lee CJ Yeo JL Cameron RH Hruban Distinctive genetic alterations in sporadic and familial adenomatous polyposis-associated pancreatoblastomas: frequent alterations in the APC/β-catenin pathway and chromosome 11p Am J Pathol 159 2001 1619 1627
    • (2001) Am J Pathol , vol.159 , pp. 1619-1627
    • Abraham, SC1    Wu, TT2    Klimstra, DS3    Finn, LS4    Lee, JH5    Yeo, CJ6    Cameron, JL7    Hruban, RH8
  • 2
    • 0023695641 scopus 로고
    • Congenital pancreatoblastoma in Beckwith-Wiedemann syndrome: an emerging association
    • R Drut MC Jones Congenital pancreatoblastoma in Beckwith-Wiedemann syndrome: an emerging association Pediatr Pathol 8 1988 331 339
    • (1988) Pediatr Pathol , vol.8 , pp. 331-339
    • Drut, R1    Jones, MC2
  • 4
    • 0022588173 scopus 로고
    • Pancreatoblastoma in a neonate associated with Beckwith-Wiedemann syndrome
    • SR Potts S Brown MD O'Hara Pancreatoblastoma in a neonate associated with Beckwith-Wiedemann syndrome Z Kinderchir 41 1986 56 57
    • (1986) Z Kinderchir , vol.41 , pp. 56-57
    • Potts, SR1    Brown, S2    O'Hara, MD3
  • 5
    • 85120202572 scopus 로고    scopus 로고
    • Kerr NJ, Chun YH, Yun K, Heathcott RW, Reeve AE, Sullivan MJ: Pancreatoblastoma is associated with chromosome 11p loss of heterozygosity and IGF2 overexpression. Med Paed Oncol 2001, in press
  • 6
    • 0030900696 scopus 로고    scopus 로고
    • Stabilization of beta-catenin by genetic defects in melanoma cell lines
    • B Rubbinfeld P Robbins M El-Gamil I Albert E Porfiri P Polakis Stabilization of beta-catenin by genetic defects in melanoma cell lines Science 275 1997 1790 1792
    • (1997) Science , vol.275 , pp. 1790-1792
    • Rubbinfeld, B1    Robbins, P2    El-Gamil, M3    Albert, I4    Porfiri, E5    Polakis, P6
  • 7
    • 0029979793 scopus 로고    scopus 로고
    • Somatic mutations of the APC gene in sporadic hepatoblastoma
    • H Oda Y Imai Y Nakatsura J Hata T Ishikawa Somatic mutations of the APC gene in sporadic hepatoblastoma Cancer Res 56 1996 3320 3323
    • (1996) Cancer Res , vol.56 , pp. 3320-3323
    • Oda, H1    Imai, Y2    Nakatsura, Y3    Hata, J4    Ishikawa, T5
  • 8
    • 0035152551 scopus 로고    scopus 로고
    • Distinctive genetic alterations in sporadic and familial adenomatous polyposis-associated pancreatoblastomas: frequent alterations in the APC/β-catenin pathway and chromosome 11p
    • SC Abraham TT Wu DS Klimstra LS Finn JH Lee CJ Yeo JL Cameron RH Hruban Distinctive genetic alterations in sporadic and familial adenomatous polyposis-associated pancreatoblastomas: frequent alterations in the APC/β-catenin pathway and chromosome 11p Am J Pathol 159 2001 1619 1627
    • (2001) Am J Pathol , vol.159 , pp. 1619-1627
    • Abraham, SC1    Wu, TT2    Klimstra, DS3    Finn, LS4    Lee, JH5    Yeo, CJ6    Cameron, JL7    Hruban, RH8
  • 9
    • 85120211440 scopus 로고    scopus 로고
    • Kerr NJ, Chun YH, Yun K, Heathcott RW, Reeve AE, Sullivan MJ: Pancreatoblastoma is associated with chromosome 11p loss of heterozygosity and IGF2 overexpression. Med Paed Oncol 2001, in press
  • 11
    • 0029979793 scopus 로고    scopus 로고
    • Somatic mutations of the APC gene in sporadic hepatoblastoma
    • H Oda Y Imai Y Nakatsura J Hata T Ishikawa Somatic mutations of the APC gene in sporadic hepatoblastoma Cancer Res 56 1996 3320 3323
    • (1996) Cancer Res , vol.56 , pp. 3320-3323
    • Oda, H1    Imai, Y2    Nakatsura, Y3    Hata, J4    Ishikawa, T5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.