4.5 Article

Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome

Related references

Note: Only part of the references are listed.
Article Endocrinology & Metabolism

The Endemic Paraganglioma Syndrome Type 1: Origin, Spread, and Clinical Expression

Francesca Schiavi et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)

Article Endocrinology & Metabolism

SDHA Immunohistochemistry Detects Germline SDHA Gene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas

Esther Korpershoek et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2011)

Review Biotechnology & Applied Microbiology

Mitochondrial diseases and the role of the yeast models

Teresa Rinaldi et al.

FEMS YEAST RESEARCH (2010)

Article Biochemistry & Molecular Biology

SDHA is a tumor suppressor gene causing paraganglioma

Nelly Burnichon et al.

HUMAN MOLECULAR GENETICS (2010)

Article Biochemical Research Methods

In vivo analysis of mtDNA replication defects in yeast

Enrico Baruffini et al.

METHODS (2010)

Article Biochemistry & Molecular Biology

Succinate inhibition of α-ketoglutarate-dependent enzymes in a yeast model of paraganglioma

Emily H. Smith et al.

HUMAN MOLECULAR GENETICS (2007)

Article Biochemistry & Molecular Biology

The role of Sdh4p Tyr-89 in ubiquinone reduction by the Saccharomyces cerevisiae succinate dehydrogenase

Yuri Sitkin et al.

BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2007)

Article Biochemical Research Methods

Quick and easy yeast transformation using the LiAc/SS carrier DNA/PEG method

R. Daniel Gietz et al.

NATURE PROTOCOLS (2007)

Review Biochemistry & Molecular Biology

Mitochondrial DNA mutations in human cancer

A. Chatterjee et al.

ONCOGENE (2006)

Article Clinical Neurology

Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA)

R Horvath et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2006)

Article Medicine, General & Internal

Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene

F Schiavi et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2005)

Article Medicine, General & Internal

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations

HPH Neumann et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2004)

Correction Medicine, General & Internal

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations (vol 292, pg 943, 2004)

HPH Neumann

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2004)

Letter Oncology

G12S and H50R variations are polymorphisms in the SDHD gene

A Cascón et al.

GENES CHROMOSOMES & CANCER (2003)

Article Biochemistry & Molecular Biology

Human non-synonymous SNPs: server and survey

V Ramensky et al.

NUCLEIC ACIDS RESEARCH (2002)

Review Biochemistry & Molecular Biology

The Saccharomyces cerevisiae mitochondrial succinate:ubiquinone oxidoreductase

BD Lemire et al.

BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2002)

Article Genetics & Heredity

Mutations in SDHC cause autosomal dominant paraganglioma, type 3

S Niemann et al.

NATURE GENETICS (2000)

Article Multidisciplinary Sciences

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

BE Baysal et al.

SCIENCE (2000)