Bora E. Baysal
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Alıntı yapanlar
Alıntı yapanlar
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
BE Baysal, RE Ferrell, JE Willett-Brozick, EC Lawrence, D Myssiorek, ...
Science 287 (5454), 848-851, 2000
Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas
BE Baysal, JE Willett-Brozick, EC Lawrence, CM Drovdlic, SA Savul, ...
Journal of medical genetics 39 (3), 178-183, 2002
Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene
F Schiavi, CC Boedeker, B Bausch, M Peçzkowska, CF Gomez, ...
Jama 294 (16), 2057-2063, 2005
Hereditary paraganglioma targets diverse paraganglia
BE Baysal
Journal of medical genetics 39 (9), 617-622, 2002
Centrifugal enhancement of retroviral mediated gene transfer
AB Bahnson, JT Dunigan, BE Baysal, T Mohney, RW Atchison, ...
Journal of virological methods 54 (2-3), 131-143, 1995
Revisiting the TCA cycle: signaling to tumor formation
N Raimundo, BE Baysal, GS Shadel
Trends in molecular medicine 17 (11), 641-649, 2011
Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene
PEM Taschner, JC Jansen, BE Baysal, A Bosch, EH Rosenberg, ...
Genes, Chromosomes and Cancer 31 (3), 274-281, 2001
Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect
K Astrom, JE Cohen, JE Willett-Brozick, CE Aston, BE Baysal
Human genetics 113 (3), 228-237, 2003
APOBEC3A cytidine deaminase induces RNA editing in monocytes and macrophages
S Sharma, SK Patnaik, RT Taggart, ED Kannisto, SM Enriquez, P Gollnick, ...
Nature communications 6 (1), 1-15, 2015
Genetics of carney triad: recurrent losses at chromosome 1 but lack of germline mutations in genes associated with paragangliomas and gastrointestinal stromal tumors
L Matyakhina, TA Bei, SR McWhinney, B Pasini, S Cameron, B Gunawan, ...
The Journal of Clinical Endocrinology & Metabolism 92 (8), 2938-2943, 2007
On the association of succinate dehydrogenase mutations with hereditary paraganglioma
BE Baysal
Trends in Endocrinology & Metabolism 14 (10), 453-459, 2003
Familial malignant catecholamine-secreting paraganglioma with prolonged survival associated with mutation in the succinate dehydrogenase B gene
AL Young, BE Baysal, A Deb, WF Young Jr
The Journal of Clinical Endocrinology & Metabolism 87 (9), 4101-4105, 2002
Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.
BE Baysal, JE Farr, WS Rubinstein, RA Galus, KA Johnson, CE Aston, ...
American journal of human genetics 60 (1), 121, 1997
Biochemically Silent Abdominal Paragangliomas in Patients with Mutations in the Succinate Dehydrogenase Subunit B Gene
HJLM Timmers, K Pacak, TT Huynh, M Abu-Asab, M Tsokos, MJ Merino, ...
The Journal of Clinical Endocrinology & Metabolism 93 (12), 4826-4832, 2008
Clinical and molecular progress in hereditary paraganglioma
BE Baysal
Journal of medical genetics 45 (11), 689-694, 2008
An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma
BE Baysal, JE Willett-Brozick, EC Lawrence, EN Myers, RE Ferrell
Journal of medical genetics 41 (9), 703-709, 2004
Loss of distal 11q is associated with DNA repair deficiency and reduced sensitivity to ionizing radiation in head and neck squamous cell carcinoma
RA Parikh, JS White, X Huang, DW Schoppy, BE Baysal, R Baskaran, ...
Genes, Chromosomes and Cancer 46 (8), 761-775, 2007
Proportion of heritable paraganglioma cases and associated clinical characteristics
CM Drovdlic, EN Myers, JA Peters, BE Baysal, DE Brackmann, ...
The Laryngoscope 111 (10), 1822-1827, 2001
Phenotypic dichotomy in mitochondrial complex II genetic disorders
BE Baysal, WS Rubinstein, PE Taschner
Journal of molecular medicine 79 (9), 495-503, 2001
Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss
RF Badenhop, S Cherian, RSA Lord, BE Baysal, PEM Taschner, ...
Genes, Chromosomes and Cancer 31 (3), 255-263, 2001
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