Cargando…

A xenograft and cell line model of SDH-deficient pheochromocytoma derived from Sdhb+/− rats

Mostrar otras versiones (1)

Detalles Bibliográficos
Autores principales:	Powers, James F, Cochran, Brent, Baleja, James D, Sikes, Hadley D, Pattison, Andrew D, Zhang, Xue, Lomakin, Inna, Shepard-Barry, Annette, Pacak, Karel, Moon, Sun Jin, Langford, Troy F, Stein, Kassi Taylor, Tothill, Richard W, Ouyang, Yingbin, Tischler, Arthur S
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Bioscientifica Ltd 2020
Materias:	Erratum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133318/ https://www.ncbi.nlm.nih.gov/pubmed/32861212 http://dx.doi.org/10.1530/ERC-19-0474e

Ejemplares similares

A xenograft and cell line model of SDH-deficient pheochromocytoma derived from Sdhb+/− rats
por: Powers, James F, et al.
Publicado: (2020)

Use of SDHB immunohistochemistry to identify germline mutations of SDH genes
por: Gill, AJ
Publicado: (2012)

Rapid Detection of SdhB(P225F) and SdhB(H272R) Mutations in Boscalid Resistant Botrytis cinerea Strains by ARMS-PCR
por: Liu, Xin, et al.
Publicado: (2019)

SDHB and SDHA Immunohistochemistry in Canine Pheochromocytomas
por: Abed, Firas M., et al.
Publicado: (2020)

Targeting NRF2-Governed Glutathione Synthesis for SDHB-Mutated Pheochromocytoma and Paraganglioma
por: Liu, Yang, et al.
Publicado: (2020)

PSUN27 Largest Cohort of Cervical Spine Metastases of Pheochromocytoma/Paraganglioma in the Setting of SDHB Mutation
por: Pacak, Karel, et al.
Publicado: (2022)

Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma
por: Hensen, Erik F., et al.
Publicado: (2010)

FRI369 SDHB Hereditary Pheochromocytoma Paraganglioma Syndrome With Biochemically Silent Pheochromocytoma
por: Skariah, Annie M, et al.
Publicado: (2023)

Pheochromocytoma in a Twelve-Year-Old Girl with SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome
por: Graham, Daryl, et al.
Publicado: (2014)

Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patients
por: Huang, Yiqiang, et al.
Publicado: (2018)

Efficacy of Immunohistochemistry for SDHB in the Screening of Hereditary Pheochromocytoma–Paraganglioma
por: Choi, Hye-Ryeon, et al.
Publicado: (2021)

The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients
por: Bayley, Jean-Pierre, et al.
Publicado: (2009)

Glutaminases as a Novel Target for SDHB-Associated Pheochromocytomas/Paragangliomas
por: Sarkadi, Balazs, et al.
Publicado: (2020)

SDHB knockout and succinate accumulation are insufficient for tumorigenesis but dual SDHB/NF1 loss yields SDHx-like pheochromocytomas
por: Armstrong, Neali, et al.
Publicado: (2022)

Metabolome Profiling by HRMAS NMR Spectroscopy of Pheochromocytomas and Paragangliomas Detects SDH Deficiency: Clinical and Pathophysiological Implications()()
por: Imperiale, Alessio, et al.
Publicado: (2015)

Fluopyram Sensitivity and Functional Characterization of SdhB in the Fusarium solani Species Complex Causing Soybean Sudden Death Syndrome
por: Sang, Hyunkyu, et al.
Publicado: (2018)

SDHB immunohistochemistry for prognosis of pheochromocytoma and paraganglioma: A retrospective and prospective analysis
por: Su, Tingwei, et al.
Publicado: (2023)

Detection of sdhB Gene Mutations in SDHI-Resistant Isolates of Botrytis cinerea Using High Resolution Melting (HRM) Analysis
por: Samaras, Anastasios, et al.
Publicado: (2016)

SUN-344 SDHB Immunostaining: Still an Indispensable Tool in Characterising Pheochromocytoma and Paraganglioma
por: Velusamy, Anand, et al.
Publicado: (2019)

Characterization and metabolic synthetic lethal testing in a new model of SDH-loss familial pheochromocytoma and paraganglioma
por: Smestad, John, et al.
Publicado: (2017)

Cytocidal Activities of Topoisomerase 1 Inhibitors and 5-Azacytidine against Pheochromocytoma/Paraganglioma Cells in Primary Human Tumor Cultures and Mouse Cell Lines
por: Powers, James F., et al.
Publicado: (2014)

Dutch founder SDHB exon 3 deletion in patients with pheochromocytoma-paraganglioma in South Africa
por: Gordon, Debra M, et al.
Publicado: (2021)

SDHB-Associated Paraganglioma in a Pediatric Patient and Literature Review on Hereditary Pheochromocytoma-Paraganglioma Syndromes
por: Choat, Heather, et al.
Publicado: (2014)

Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients
por: Bennedbæk, Marc, et al.
Publicado: (2016)

International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma
por: Ben Aim, Laurene, et al.
Publicado: (2022)

Increased expression of Nrf2 and elevated glucose uptake in pheochromocytoma and paraganglioma with SDHB gene mutation
por: Kamai, Takao, et al.
Publicado: (2022)

Long-term in vitro 2D-culture of SDHB and SDHD-related human paragangliomas and pheochromocytomas
por: Bayley, Jean-Pierre, et al.
Publicado: (2022)

SDHB exon 1 deletion: A recurrent germline mutation in Colombian patients with pheochromocytomas and paragangliomas
por: Manotas, María Carolina, et al.
Publicado: (2023)

Novel and recurrent genetic variants of VHL, SDHB, and RET genes in Chinese pheochromocytoma and paraganglioma patients
por: Li, Chong, et al.
Publicado: (2023)

The size of the primary tumor and age at initial diagnosis are independent predictors of the metastatic behavior and survival of patients with SDHB-related pheochromocytoma and paraganglioma: a retrospective cohort study
por: Schovanek, Jan, et al.
Publicado: (2014)

Composite pheochromocytoma/paraganglioma-ganglioneuroma: analysis of SDH and ATRX status, and identification of frequent HRAS and BRAF mutations
por: Chen, Jingci, et al.
Publicado: (2021)

Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironment
por: Zethoven, Magnus, et al.
Publicado: (2022)

OR34-6 A Novel Mechanism of SDH-Deficient Tumorigenesis and Implications for Genetic Testing in Patients with Pheochromocytoma-Paraganglioma
por: De Sousa, Sunita M.C., et al.
Publicado: (2019)

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
por: Bayley, Jean-Pierre, et al.
Publicado: (2006)

Author Correction: Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironment
por: Zethoven, Magnus, et al.
Publicado: (2023)

Bayesian approach to determining penetrance of pathogenic SDH variants
por: Benn, Diana E, et al.
Publicado: (2018)

Radio digital SDH/
por: Castellanos Moreno, Fabiola Melina
Publicado: (2001)

Pheochromocytoma (PHEO) and Paraganglioma (PGL)
por: Pacak, Karel, et al.
Publicado: (2019)

The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency
por: Bayley, Jean-Pierre, et al.
Publicado: (2005)

THU612 SDHx Pheochromocytoma/Paraganglioma Has Elevation Of Arginine And Lysine Metabolites
por: Ghayee, Hans Kumar, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_vmc4g9ds071ee3jp9ljutcah9h