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K Gwinn

Showing results (21-30 of 49) with videos related to

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Biochemical Society Transactions|July 27, 2005
Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiensJ Hardy, A Pittman, A Myers, et al.
Acta Neuropathologica|June 27, 2000
Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4pK Gwinn-Hardy, N D Mehta, M Farrer, et al.
Inorganic Chemistry|January 24, 2025
Lewis Base-Enhanced C-H Bond Functionalization Mediated by a Diiron Imido ComplexReilly K Gwinn, Trevor P Latendresse, Owen N Beck, et al.
Archives of Neurology|February 15, 2001
Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black familyK Gwinn-Hardy, A Singleton, P O'Suilleabhain, et al.
Organic Letters|January 29, 2026
Phosphine-Catalyzed Regio- and Stereoselective Umpolung Addition of Amides to Alkynoates: Access to Complex α,β-Dehydroamino Acid DerivativesNicklas W Buchbinder, Kyle L Dunnavant, Andrew D Bage, et al.
Bioorganic & Medicinal Chemistry Letters|February 2, 2026
Substituted 1-(benzo[d]thiazol-2-yl)-3-phenylurea derivatives as anti-invasion agentsReilly K Gwinn, Padmanabhan Mannangatti, Shahid Maqbool Mir, et al.
American Journal of Medical Genetics|June 5, 1998
Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonismJ Hardy, J Pérez-Tur, M Baker, et al.
Annals of Neurology|March 20, 1998
Low frequency of alpha-synuclein mutations in familial Parkinson's diseaseM Farrer, F Wavrant-De Vrieze, R Crook, et al.
Neuroscience Letters|August 3, 1999
No pathogenic mutations in the beta-synuclein gene in Parkinson's diseaseS Lincoln, R Crook, M C Chartier-Harlin, et al.
Neuroscience Letters|January 19, 2007
BDNF tagging polymorphisms and haplotype analysis in sporadic Parkinson's disease in diverse ethnic groupsG Xiromerisiou, G M Hadjigeorgiou, J Eerola, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Biochemical Society Transactions|July 27, 2005
Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiensJ Hardy, A Pittman, A Myers, et al.
Acta Neuropathologica|June 27, 2000
Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4pK Gwinn-Hardy, N D Mehta, M Farrer, et al.
Inorganic Chemistry|January 24, 2025
Lewis Base-Enhanced C-H Bond Functionalization Mediated by a Diiron Imido ComplexReilly K Gwinn, Trevor P Latendresse, Owen N Beck, et al.
Archives of Neurology|February 15, 2001
Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black familyK Gwinn-Hardy, A Singleton, P O'Suilleabhain, et al.
Organic Letters|January 29, 2026
Phosphine-Catalyzed Regio- and Stereoselective Umpolung Addition of Amides to Alkynoates: Access to Complex α,β-Dehydroamino Acid DerivativesNicklas W Buchbinder, Kyle L Dunnavant, Andrew D Bage, et al.
Bioorganic & Medicinal Chemistry Letters|February 2, 2026
Substituted 1-(benzo[d]thiazol-2-yl)-3-phenylurea derivatives as anti-invasion agentsReilly K Gwinn, Padmanabhan Mannangatti, Shahid Maqbool Mir, et al.
American Journal of Medical Genetics|June 5, 1998
Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonismJ Hardy, J Pérez-Tur, M Baker, et al.
Annals of Neurology|March 20, 1998
Low frequency of alpha-synuclein mutations in familial Parkinson's diseaseM Farrer, F Wavrant-De Vrieze, R Crook, et al.
Neuroscience Letters|August 3, 1999
No pathogenic mutations in the beta-synuclein gene in Parkinson's diseaseS Lincoln, R Crook, M C Chartier-Harlin, et al.
Neuroscience Letters|January 19, 2007
BDNF tagging polymorphisms and haplotype analysis in sporadic Parkinson's disease in diverse ethnic groupsG Xiromerisiou, G M Hadjigeorgiou, J Eerola, et al.
Pageof 5