相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Allelic variant at-79 (C>T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels
Inigo Landa et al.
ENDOCRINE-RELATED CANCER (2010)
SDHA is a tumor suppressor gene causing paraganglioma
Nelly Burnichon et al.
HUMAN MOLECULAR GENETICS (2010)
Spectrum and Prevalence of FP/TMEM127 Gene Mutations in Pheochromocytomas and Paragangliomas
Li Yao et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2010)
Research Resource: Transcriptional Profiling Reveals Different Pseudohypoxic Signatures in SDHB and VHL-Related Pheochromocytomas
Elena Lopez-Jimenez et al.
MOLECULAR ENDOCRINOLOGY (2010)
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma
Yuejuan Qin et al.
NATURE GENETICS (2010)
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
Kai Wang et al.
NUCLEIC ACIDS RESEARCH (2010)
Regulation of Gene Expression in Hepatic Cells by the Mammalian Target of Rapamycin (mTOR)
Rosa H. Jimenez et al.
PLOS ONE (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Genetics of Pheochromocytoma and Paraganglioma in Spanish Patients
Alberto Cascon et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)
Clinically Guided Genetic Screening in a Large Cohort of Italian Patients with Pheochromocytomas and/or Functional or Nonfunctional Paragangliomas
Massimo Mannelli et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)
New Lesions Detected by Single Nucleotide Polymorphism Array-Based Chromosomal Analysis Have Important Clinical Impact in Acute Myeloid Leukemia
Ramon V. Tiu et al.
JOURNAL OF CLINICAL ONCOLOGY (2009)
The Warburg Effect Is Genetically Determined in Inherited Pheochromocytomas
Judith Favier et al.
PLOS ONE (2009)
SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma
Huai-Xiang Hao et al.
SCIENCE (2009)
c-Myc inhibits Ras-mediated differentiation of pheochromocytoma cells by blocking c-Jun up-regulation
Jose P. Vaque et al.
MOLECULAR CANCER RESEARCH (2008)
Activation of PI3K/Akt and MAPK pathways regulates Myc-mediated transcription by phosphorylating and promoting the degradation of Mad1
Jidong Zhu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: Two new reports
Meredith Wilson et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals
Javier Simon-Sanchez et al.
HUMAN MOLECULAR GENETICS (2007)
Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR:: A possible hot spot?
A Cascón et al.
GENES CHROMOSOMES & CANCER (2006)
Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event
MT Teh et al.
CANCER RESEARCH (2005)
A HIF1α regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas
PLM Dahia et al.
PLOS GENETICS (2005)
The NF1 tumor suppressor critically regulates TSC2 and mTOR
CM Johannessen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia:: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour
D Astuti et al.
BRITISH JOURNAL OF CANCER (2005)
X-ray structures of Myc-Max and Mad-Max recognizing DNA: Molecular bases of regulation by proto-oncogenic transcription factors
SK Nair et al.
CELL (2003)
Loss of heterozygosity associated with uniparental disomy in breast carcinoma
SK Murthy et al.
MODERN PATHOLOGY (2002)
Paternal UPD14 is responsible for a distinctive malformation complex
K Kurosawa et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Germ-line mutations in nonsyndromic pheochromocytoma.
HPH Neumann et al.
NEW ENGLAND JOURNAL OF MEDICINE (2002)
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
BE Baysal et al.
SCIENCE (2000)
Transforming ability of MEN2A-RET requires activation of the phosphatidylinositol 3-kinase/AKT signaling pathway
C Segouffin-Cariou et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
分享论文
