Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas.
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Yih-Leong Chang | P. Lou | Tsung-Lin Yang | Pei-Lung Chen | Tseng-Cheng Chen | Cheng-Ping Wang | J. Ko | Ya-Ling Hu | Fei-Yun Lo | Chen-Chi Wu
[1] R. Ramos,et al. Mutation of SDHB is a Cause of Hypoxia-Related High-Altitude Paraganglioma , 2010, Clinical Cancer Research.
[2] A. Chou,et al. Immunohistochemistry for SDHB triages genetic testing of SDHB, SDHC, and SDHD in paraganglioma-pheochromocytoma syndromes. , 2010, Human pathology.
[3] Steven P. Gygi,et al. SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma , 2009, Science.
[4] E. van Marck,et al. An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis. , 2009, The Lancet. Oncology.
[5] C. Stratakis,et al. SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma–paraganglioma syndromes , 2009, Journal of internal medicine.
[6] K. Pacak,et al. Clinical aspects of SDHx-related pheochromocytoma and paraganglioma. , 2009, Endocrine-related cancer.
[7] M. Weiss,et al. Chromosomal changes in sporadic and familial head and neck paragangliomas , 2009, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.
[8] O. Haas,et al. Novel SDHD germ‐line mutations in pheochromocytoma patients , 2007, European journal of clinical investigation.
[9] R. Ma,et al. A Chinese family with familial paraganglioma syndrome due to succinate dehydrogenase deficiency. , 2007, Hong Kong medical journal = Xianggang yi xue za zhi.
[10] Peter Devilee,et al. The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency , 2005, BMC Medical Genetics.
[11] M. Mascalchi,et al. Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109X , 2005, Journal of Medical Genetics.
[12] J. Netterville,et al. Paragangliomas of the head and neck. , 2004, Oral oncology.
[13] K. Sotlar,et al. Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. , 2004, Cancer genetics and cytogenetics.
[14] P. Taschner,et al. Hereditary Paraganglioma Due to the SDHD M1I Mutation in a Second Chinese Family: A Founder Effect? , 2003, The Laryngoscope.
[15] W. Dinjens,et al. Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma. , 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.
[16] E S Husebye,et al. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. , 2001, American journal of human genetics.
[17] P. Schofield,et al. Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss , 2001, Genes, chromosomes & cancer.
[18] P. Devilee,et al. Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene , 2001, Genes, chromosomes & cancer.
[19] Ulrich Müller,et al. Mutations in SDHC cause autosomal dominant paraganglioma, type 3 , 2000, Nature Genetics.
[20] B. Devlin,et al. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. , 2000, Science.