Prevalence of RET protooncogene mutations in sporadic pheochromocytomas

被引：0
|
作者：
Gregg, JP [1 ]
Yamane, AJ [1 ]
Nakaichi, GK [1 ]
Gatti, RA [1 ]
Grody, WW [1 ]
机构：
[1] UNIV CALIF LOS ANGELES,SCH MED,DEPT MOLEC GENET & PATHOL,LOS ANGELES,CA
来源：
LABORATORY INVESTIGATION | 1996年 / 74卷 / 01期
关键词：
D O I：
暂无
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
引用
收藏
页码：266 / 266
页数：1
相关论文
共 50 条
  • [1] MUTATIONS IN THE RET PROTOONCOGENE IN SPORADIC PHEOCHROMOCYTOMAS
    LINDOR, NM
    HONCHEL, R
    KHOSLA, S
    THIBODEAU, SN
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (02): : 627 - 629
  • [2] Sporadic pheochromocytomas are rarely associated with germline mutations in the vhl tumor suppressor gene or the ret protooncogene
    Brauch, H
    Hoeppner, W
    Jähnig, H
    Wöhl, T
    Engelhardt, D
    Spelsberg, F
    Ritter, MM
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (12): : 4101 - 4104
  • [3] TUMOR-SPECIFIC MUTATIONS IN THE TYROSINE KINASE DOMAIN OF THE RET PROTOONCOGENE IN PHEOCHROMOCYTOMAS OF SPORADIC TYPE
    YOSHIMOTO, K
    TANAKA, C
    HAMAGUCHI, S
    KIMURA, T
    IWAHANA, H
    MIYAUCHI, A
    ITAKURA, M
    ENDOCRINE JOURNAL, 1995, 42 (02) : 265 - 270
  • [4] RET mutations in sporadic malignant pheochromocytomas.
    deKrijger, RR
    vanderHarst, E
    MulettaFeurer, S
    Bruining, HA
    Lamberts, SWJ
    Komminoth, P
    LABORATORY INVESTIGATION, 1997, 76 (01) : 269 - 269
  • [5] THE RET PROTOONCOGENE IN SPORADIC PHEOCHROMOCYTOMAS - FREQUENT MEN 2-LIKE MUTATIONS AND NEW MOLECULAR DEFECTS
    BELDJORD, C
    DESCLAUXARRAMOND, F
    RAFFINSANSON, M
    CORVOL, JC
    DEKEYZER, Y
    LUTON, JP
    PLOUIN, PF
    BERTAGNA, X
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (07): : 2063 - 2068
  • [6] MUTATIONS IN THE RET PROTOONCOGENE AND THE VON HIPPEL-LINDAU DISEASE TUMOR-SUPPRESSOR GENE IN SPORADIC AND SYNDROMIC PHEOCHROMOCYTOMAS
    ENG, C
    CROSSEY, PA
    MULLIGAN, LM
    HEALEY, CS
    HOUGHTON, C
    PROWSE, A
    CHEW, SL
    DAHIA, PLM
    ORIORDAN, JLH
    TOLEDO, SPA
    SMITH, DP
    MAHER, ER
    PONDER, BAJ
    JOURNAL OF MEDICAL GENETICS, 1995, 32 (12) : 934 - 937
  • [7] DIVERSITY OF RET PROTOONCOGENE MUTATIONS IN FAMILIAL AND SPORADIC HIRSCHSPRUNG DISEASE
    ATTIE, T
    PELET, A
    EDERY, P
    ENG, C
    MULLIGAN, LM
    AMIEL, J
    BOUTRAND, L
    BELDJORD, C
    NIHOULFEKETE, C
    MUNNICH, A
    PONDER, BAJ
    LYONNET, S
    HUMAN MOLECULAR GENETICS, 1995, 4 (08) : 1381 - 1386
  • [8] RET protooncogene mutations in patients with apparently sporadic medullary thyroid carcinoma
    Huang, CN
    Wu, SL
    Chang, TC
    Huang, SH
    Chang, TJ
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 1998, 97 (08) : 541 - 546
  • [9] RET PROTOONCOGENE MUTATIONS IN INHERITED AND SPORADIC MEDULLARY-THYROID CANCER
    BLAUGRUND, JE
    JOHNS, MM
    EBY, YJ
    BALL, DW
    BAYLIN, SB
    HRUBAN, RH
    SIDRANSKY, D
    HUMAN MOLECULAR GENETICS, 1994, 3 (10) : 1895 - 1897
  • [10] Mutations and polymorphisms in the SDHB, SDHD, VHL, and RET genes in sporadic and familial pheochromocytomas
    Jens Waldmann
    Peter Langer
    Nils Habbe
    Volker Fendrich
    Anette Ramaswamy
    Matthias Rothmund
    Detlef K. Bartsch
    Emily P. Slater
    Endocrine, 2009, 35 : 347 - 355
12345