Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function

Proteomic identification of glutamine synthetase as a differential marker for oligodendrogliomas and astrocytomas

(2011) Zhengping Zhuang et al.   JOURNAL OF NEUROSURGERY

A continuum model for tumour suppression

(2011) Alice H. Berger et al.   NATURE

Renal Tumors and Hereditary Pheochromocytoma-Paraganglioma Syndrome Type 4

(2011) Anthony J. Gill et al.   NEW ENGLAND JOURNAL OF MEDICINE

Missense mutations in the NF2 gene result in the quantitative loss of merlin protein and minimally affect protein intrinsic function

(2011) C. Yang et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Pheochromocytomas: The (pseudo)-hypoxia hypothesis

(2010) Judith Favier et al.   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

Tyrosine hydroxylase, chromogranin A, and steroidogenic acute regulator as markers for successful separation of human adrenal medulla

(2010) Stephanie M. J. Fliedner et al.   CELL AND TISSUE RESEARCH

Mutation analysis of HIF prolyl hydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility

(2010) D. Astuti et al.   ENDOCRINE-RELATED CANCER

Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma

(2010) Erik F. Hensen et al.   Familial Cancer

Inter-connection between mitochondria and HIFs

(2010) Kathryn V. Tormos et al.   JOURNAL OF CELLULAR AND MOLECULAR MEDICINE

Decreased glucocerebrosidase activity in Gaucher disease parallels quantitative enzyme loss due to abnormal interaction with TCP1 and c-Cbl

(2010) J. Lu et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

SDHB-associated renal oncocytoma suggests a broadening of the renal phenotype in hereditary paragangliomatosis

(2009) Alex Henderson et al.   Familial Cancer

Tumor risks and genotype–phenotype–proteotype analysis in 358 patients with germline mutations inSDHBandSDHD

(2009) Christopher J. Ricketts et al.   HUMAN MUTATION

An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis

(2009) Francien H van Nederveen et al.   LANCET ONCOLOGY

Treatment of malignant pheochromocytoma/paraganglioma with cyclophosphamide, vincristine, and dacarbazine

(2008) Hui Huang et al.   CANCER

Germline SDHB Mutations and Familial Renal Cell Carcinoma

(2008) C. Ricketts et al.   JNCI-Journal of the National Cancer Institute