scholarly journals Identification and characterization of a novel germ line p53 mutation in familial gastric cancer in the Japanese population

2007 ◽  
Vol 28 (9) ◽  
pp. 2013-2018 ◽  
Author(s):  
H. Yamada ◽  
K. Shinmura ◽  
K. Okudela ◽  
M. Goto ◽  
M. Suzuki ◽  
...  
2011 ◽  
Vol 102 (10) ◽  
pp. 1782-1788 ◽  
Author(s):  
Hidetaka Yamada ◽  
Kazuya Shinmura ◽  
Hiroaki Ito ◽  
Masako Kasami ◽  
Naomi Sasaki ◽  
...  

2015 ◽  
Vol 10 (1) ◽  
pp. 329-336 ◽  
Author(s):  
ZHAOFENG CHEN ◽  
XIAOGUANG LIU ◽  
ZENAN HU ◽  
YUPING WANG ◽  
MIN LIU ◽  
...  

Hematology ◽  
2016 ◽  
Vol 2016 (1) ◽  
pp. 293-301 ◽  
Author(s):  
Rose B. McGee ◽  
Kim E. Nichols

AbstractThe last 30 years have witnessed tremendous advances in our understanding of the cancer genetic susceptibility syndromes, including those that predispose to hematopoietic malignancies. The identification and characterization of families affected by these syndromes is enhancing our knowledge of the oncologic and nononcologic manifestations associated with predisposing germ line mutations and providing insights into the underlying disease mechanisms. Here, we provide an overview of the cancer genetic susceptibility syndromes, focusing on aspects relevant to the evaluation of patients with leukemia and lymphoma. Guidance is provided to facilitate recognition of these syndromes by hematologists/oncologists, including descriptions of the family history features, tumor genotype, and physical or developmental findings that should raise concern for an underlying cancer genetic syndrome. The clinical implications and management challenges associated with cancer susceptibility syndromes are also discussed.


Tumor Biology ◽  
1999 ◽  
Vol 20 (5) ◽  
pp. 235-241 ◽  
Author(s):  
Hideki Kakiuchi ◽  
Fumio Itoh ◽  
Masanobu Kusano ◽  
Yasushi Adachi ◽  
Hiroaki Mita ◽  
...  

2010 ◽  
Vol 42 ◽  
pp. S139
Author(s):  
A. Rocco ◽  
E. Liguori ◽  
G. Pirozzi ◽  
V. Tirino ◽  
A. Affuso ◽  
...  

Oncogene ◽  
2007 ◽  
Vol 26 (52) ◽  
pp. 7371-7379 ◽  
Author(s):  
X Xu ◽  
W Li ◽  
X Fan ◽  
Y Liang ◽  
M Zhao ◽  
...  

PLoS ONE ◽  
2015 ◽  
Vol 10 (6) ◽  
pp. e0130808 ◽  
Author(s):  
Takeshi Fujita ◽  
Fumiko Chiwaki ◽  
Ryou-u Takahashi ◽  
Kazuhiko Aoyagi ◽  
Kazuyoshi Yanagihara ◽  
...  

Development ◽  
1997 ◽  
Vol 124 (16) ◽  
pp. 3055-3064 ◽  
Author(s):  
T.E. Haerry ◽  
T.R. Heslip ◽  
J.L. Marsh ◽  
M.B. O'Connor

In vitro experiments suggest that glycosaminoglycans (GAGs) and the proteins to which they are attached (proteoglycans) are important for modulating growth factor signaling. However, in vivo evidence to support this view has been lacking, in part because mutations that disrupt the production of GAG polymers and the core proteins have not been available. Here we describe the identification and characterization of Drosophila mutants in the suppenkasper (ska) gene. The ska gene encodes UDP-glucose dehydrogenase which produces glucuronic acid, an essential component for the synthesis of heparan and chondroitin sulfate. ska mutants fail to put heparan side chains on proteoglycans such as Syndecan. Surprisingly, mutant embryos produced by germ-line clones of this general metabolic gene exhibit embryonic cuticle phenotypes strikingly similar to those that result from loss-of-function mutations in genes of the Wingless (Wg) signaling pathway. Zygotic loss of ska leads to reduced growth of imaginal discs and pattern defects similar to wg mutants. In addition, genetic interactions of ska with wg and dishevelled mutants are observed. These data demonstrate the importance of proteoglycans and GAGs in Wg signaling in vivo and suggest that Wnt-like growth factors may be particularly sensitive to perturbations of GAG biosynthesis.


2004 ◽  
Vol 24 (6) ◽  
pp. 481-490 ◽  
Author(s):  
Hiroshi Yagasaki ◽  
Satoshi Hamanoue ◽  
Tsukasa Oda ◽  
Tatsutoshi Nakahata ◽  
Shigetaka Asano ◽  
...  

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