B. Giasson

发表

Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes.

J Q Trojanowski, D A Pollen, T D Bird, 1998, The American journal of pathology.

Immunohistochemical and Biochemical Studies Demonstrate a Distinct Profile of α‐Synuclein Permutations in Multiple System Atrophy

T. Montine, J. Trojanowski, M. Grossman, 2000, Journal of neuropathology and experimental neurology.

Synucleins are expressed in the majority of breast and ovarian carcinomas and in preneoplastic lesions of the ovary

J. Trojanowski, V. Lee, A. Klein-Szanto, 2000, Cancer.

Residue Glu83 Plays a Major Role in Negatively Regulating α Synuclein Amyloid Formation

E. Waxman, B. Giasson, Kristel L. Emmer, 2010 .

Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble α‐synuclein

J Q Trojanowski, J. Trojanowski, V. Lee, 1998, Annals of neurology.

Short Communication Neurodegeneration with Brain Iron Accumulation, Type 1 Is Characterized by a -, b -, and g -Synuclein Neuropathology

J. Trojanowski, V. Lee, H. Hurtig, 2000 .

DJ-1 deﬁcient mice demonstrate similar vulnerability to pathogenic Ala53Thr human a -syn toxicity

H. Ischiropoulos, B. Giasson, Elpida Tsika, 2010 .

Degradative organelles containing mislocalized (cid:1) - and (cid:2) -synuclein proliferate in presenilin-1 null neurons

Christina A. Wilson, J. Trojanowski, V. Lee, 2004 .

Biochemical and pathological characterization of Lrrk2

J. Trojanowski, M. Farrer, N. Bonini, 2006, Annals of neurology.

AMPA receptor‐mediated toxicity in oligodendrocyte progenitors involves free radical generation and activation of JNK, calpain and caspase 3

G. Almazan, B. Giasson, W. Mushynski, 2002, Journal of neurochemistry.

A panel of epitope‐specific antibodies detects protein domains distributed throughout human α‐synuclein in lewy bodies of Parkinson's disease

J. Trojanowski, V. Lee, M. Goedert, 2000, Journal of neuroscience research.

Identification and characterization of a novel endogenous murine parkin mutation

B. Giasson, B. Giasson, Chenere P. Ramsey, 2010, Journal of neurochemistry.

Distinct cleavage patterns of normal and pathologic forms of α‐synuclein by calpain I in vitro

John Q. Trojanowski, J. Trojanowski, V. Lee, 2003 .

Study of Proline-Directed Protein Kinases Involved in Phosphorylation of the Heavy Neurofilament Subunit

B. Giasson, W. Mushynski, Walter E. Mushynski, 1997, The Journal of Neuroscience.

Intermediate Filament Disassembly in Cultured Dorsal Root Ganglion Neurons Is Associated with Amino‐Terminal Head Domain Phosphorylation of Specific Subunits

B. Giasson, B. Giasson, W. Mushynski, 1998, Journal of neurochemistry.

The G2019S pathogenic mutation disrupts sensitivity of leucine‐rich repeat kinase 2 to manganese kinase inhibition

Jason P. Covy, B. Giasson, Benoit I. Giasson, 2010, Journal of neurochemistry.

Tau and 14-3-3 in glial cytoplasmic inclusions of multiple system atrophy

T. Montine, J. Trojanowski, V. Lee, 2003, Acta Neuropathologica.

L10p and P158DEL DJ‐1 mutations cause protein instability, aggregation, and dimerization impairments

B. Giasson, B. Giasson, Chenere P. Ramsey, 2010, Journal of neuroscience research.

Activation of Cyclic AMP‐Dependent Protein Kinase in Okadaic Acid‐Treated Neurons Potentiates Neurofilament Fragmentation and Stimulates Phosphorylation of Ser2 in the Low‐Molecular‐Mass Neurofilament Subunit

J. A. Cromlish, B. Giasson, W. Mushynski, 1996, Journal of neurochemistry.

Lack of evidence for Lrrk2 in α‐synuclein pathological inclusions

B. Giasson, V. V. Van Deerlin, Jason P. Covy, 2006 .

Is the Initial Insult in Parkinson's Disease and Dementia with Lewy Bodies a Neuritic Dystrophy?

J. Trojanowski, V. Lee, B. Giasson, 2003 .