Related references
Note: Only part of the references are listed.Increased levels of copper efflux transporter ATP7B are associated with poor outcome in colorectal cancer patients receiving oxaliplatin-based chemotherapy
Eva Martinez-Balibrea et al.
INTERNATIONAL JOURNAL OF CANCER (2009)
Identification of novel ATP7B gene mutations and their functional roles in Korean patients with Wilson disease
Sangwook Park et al.
HUMAN MUTATION (2007)
Trafficking of the copper-ATPases, ATP7A and ATP7B: Role in copper homeostasis
Sharon La Fontaine et al.
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS (2007)
The roles of copper transporters in cisplatin resistance
Macus Tien Kuo et al.
CANCER AND METASTASIS REVIEWS (2007)
Role of copper transporters in the uptake and efflux of platinum containing drugs
R Safaei
CANCER LETTERS (2006)
Expression of copper-transporting P-type adenosine triphosphatase (ATP7B) as a prognostic factor in human endometrial carcinoma
T Aida et al.
GYNECOLOGIC ONCOLOGY (2005)
Prognostic value of the Cu-transporting ATPase in ovarian carcinoma patients receiving cisplatin-based chemotherapy
K Nakayama et al.
CLINICAL CANCER RESEARCH (2004)
Increased expression of the copper efflux transporter ATP7A mediates resistance to cisplatin, carboplatin, and oxaliplatin in ovarian cancer cells
G Samimi et al.
CLINICAL CANCER RESEARCH (2004)
Modulation of the cellular pharmacology of cisplatin and its analogs by the copper exporters ATP7A and ATP7B
G Samimi et al.
MOLECULAR PHARMACOLOGY (2004)
Mutation spectrum and polymorphisms in ATP7B identified on direct sequencing of all exons in Chinese Han and Hui ethnic patients with Wilson's disease
YH Gu et al.
CLINICAL GENETICS (2003)
The copper export pump ATP7B modulates the cellular pharmacology of carboplatin in ovarian carcinoma cells
K Katano et al.
MOLECULAR PHARMACOLOGY (2003)
Presymptomatic diagnosis of Wilson disease associated with a novel mutation of the ATP7B gene
K Ohya et al.
EUROPEAN JOURNAL OF PEDIATRICS (2002)
Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association
CC Lee et al.
JOURNAL OF HUMAN GENETICS (2000)