Page last updated: 2024-08-23

staurosporine and Parkinsonian Disorders

staurosporine has been researched along with Parkinsonian Disorders in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Chen, CM; Chen, IC; Fung, HC; Huang, SY; Kao, SH; Lee, GC; Lee-Chen, GJ; Soong, BW; Wu, YR	1
Barzaghi, C; Brusa, L; Dallapiccola, B; Ferraris, A; Garavaglia, B; Gelmetti, V; Lombardi, F; Romano, F; Stanzione, P; Valente, EM	1

Other Studies

2 other study(ies) available for staurosporine and Parkinsonian Disorders

Article	Year
SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications. Human genetics, 2009, Volume: 125, Issue:4 Topics: Adult; Aged; Aged, 80 and over; Alzheimer Disease; Base Sequence; Case-Control Studies; Cell Line; Central Nervous System Diseases; DNA Primers; Female; Gene Expression; Humans; Leupeptins; Lymphocytes; Male; Microfilament Proteins; Middle Aged; Nerve Tissue Proteins; Parkinson Disease; Parkinsonian Disorders; Polymorphism, Single Nucleotide; Pyrimidines; RNA, Long Noncoding; RNA, Untranslated; Spinocerebellar Ataxias; Staurosporine; Sulfonamides; Trinucleotide Repeat Expansion	2009
Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional study. Movement disorders : official journal of the Movement Disorder Society, 2008, Apr-30, Volume: 23, Issue:6 Topics: Aged; Female; Humans; Male; Middle Aged; Mutagenesis, Site-Directed; Mutation; Parkinsonian Disorders; Protein Kinases; Staurosporine; Transfection; Ubiquitin-Protein Ligases	2008

Article

Year

SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications.

Human genetics, 2009, Volume: 125, Issue:4

Topics: Adult; Aged; Aged, 80 and over; Alzheimer Disease; Base Sequence; Case-Control Studies; Cell Line; Central Nervous System Diseases; DNA Primers; Female; Gene Expression; Humans; Leupeptins; Lymphocytes; Male; Microfilament Proteins; Middle Aged; Nerve Tissue Proteins; Parkinson Disease; Parkinsonian Disorders; Polymorphism, Single Nucleotide; Pyrimidines; RNA, Long Noncoding; RNA, Untranslated; Spinocerebellar Ataxias; Staurosporine; Sulfonamides; Trinucleotide Repeat Expansion

2009

Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional study.

Movement disorders : official journal of the Movement Disorder Society, 2008, Apr-30, Volume: 23, Issue:6

Topics: Aged; Female; Humans; Male; Middle Aged; Mutagenesis, Site-Directed; Mutation; Parkinsonian Disorders; Protein Kinases; Staurosporine; Transfection; Ubiquitin-Protein Ligases

2008