Suely Kazue Nagahashi Marie
Suely Kazue Nagahashi Marie
Professor Associado de Medicina
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An integrated genomic analysis of human glioblastoma multiforme
DW Parsons, S Jones, X Zhang, JCH Lin, RJ Leary, P Angenendt, ...
science 321 (5897), 1807-1812, 2008
Detection of circulating tumor DNA in early-and late-stage human malignancies
C Bettegowda, M Sausen, RJ Leary, I Kinde, Y Wang, N Agrawal, ...
Science translational medicine 6 (224), 224ra24-224ra24, 2014
SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomas
AJ Bass, H Watanabe, CH Mermel, S Yu, S Perner, RG Verhaak, SY Kim, ...
Nature genetics 41 (11), 1238-1242, 2009
Altered telomeres in tumors with ATRX and DAXX mutations
CM Heaphy, RF De Wilde, Y Jiao, AP Klein, BH Edil, C Shi, C Bettegowda, ...
Science 333 (6041), 425-425, 2011
The genetic landscape of the childhood cancer medulloblastoma
DW Parsons, M Li, X Zhang, S Jones, RJ Leary, JCH Lin, SM Boca, ...
science 331 (6016), 435-439, 2011
Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas
Y Jiao, PJ Killela, ZJ Reitman, BA Rasheed, CM Heaphy, RF de Wilde, ...
Oncotarget 3 (7), 709, 2012
Mutations in CIC and FUBP1 contribute to human oligodendroglioma
C Bettegowda, N Agrawal, Y Jiao, M Sausen, LD Wood, RH Hruban, ...
Science 333 (6048), 1453-1455, 2011
Evaluation of DNA from the Papanicolaou test to detect ovarian and endometrial cancers
I Kinde, C Bettegowda, Y Wang, J Wu, N Agrawal, IM Shih, R Kurman, ...
Science translational medicine 5 (167), 167ra4-167ra4, 2013
Transcriptomic analysis of purified human cortical microglia reveals age-associated changes
TF Galatro, IR Holtman, AM Lerario, ID Vainchtein, N Brouwer, PR Sola, ...
Nature neuroscience 20 (8), 1162, 2017
UK biobank data: come and get it
NE Allen, C Sudlow, T Peakman, R Collins
Science translational medicine 6 (224), 224ed4-224ed4, 2014
Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV)
S Rosemberg, SKN Marie, S Kliemann
Pediatric neurology 11 (1), 50-56, 1994
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies
M Vainzof, MR Passos-Bueno, M Canovas, ES Moreira, RCM Pavanello, ...
Human molecular genetics 5 (12), 1963-1969, 1996
Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord
Y Wang, S Springer, M Zhang, KW McMahon, I Kinde, L Dobbyn, J Ptak, ...
Proceedings of the National Academy of Sciences 112 (31), 9704-9709, 2015
Selection of suitable housekeeping genes for expression analysis in glioblastoma using quantitative RT-PCR
V Valente, SA Teixeira, L Neder, OK Okamoto, SM Oba-Shinjo, ...
BMC molecular biology 10 (1), 17, 2009
Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders
K Mamchaoui, C Trollet, A Bigot, E Negroni, S Chaouch, A Wolff, ...
Skeletal muscle 1 (1), 34, 2011
The 10 autosomal recessive limb-girdle muscular dystrophies
M Zatz, F de Paula, A Starling, M Vainzof
Neuromuscular disorders 13 (7-8), 532-544, 2003
PIK3CA gene mutations in pediatric and adult glioblastoma multiforme
GL Gallia, V Rand, IM Siu, CG Eberhart, CD James, SKN Marie, ...
Molecular Cancer Research 4 (10), 709-714, 2006
New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
TC Pan, RZ Zhang, DG Sudano, SK Marie, CG Bönnemann, ML Chu
The American Journal of Human Genetics 73 (2), 355-369, 2003
Effects of somatosensory stimulation on motor function in chronic cortico-subcortical strokes
AB Conforto, LG Cohen, RL Dos Santos, M Scaff, SKN Marie
Journal of neurology 254 (3), 333-339, 2007
The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome
AA Camargo, HPB Samaia, E Dias-Neto, DF Simão, IA Migotto, ...
Proceedings of the National Academy of Sciences 98 (21), 12103-12108, 2001
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Artiklar 1–20