Výsledky vyhledávání - Massimo Pandolfo
- Zobrazuji výsledky 1 - 20 z 65
- Přejít na další stránku
-
1
-
2
-
3
-
4
-
5
-
6
Pharmacological treatments for Friedreich ataxia Autor Mary Kearney, Richard W. Orrell, Michael Fahey, Ruth Brassington, Massimo Pandolfo
Vydáno 2016Revisão -
7
-
8
-
9
-
10
-
11
-
12
-
13
GGA·TCC-interrupted Triplets in Long GAA·TTC Repeats Inhibit the Formation of Triplex and Sticky DNA Structures, Alleviate Transcription Inhibition, and Reduce Genetic Instabilitie... Autor Naoaki Sakamoto, Jacquelynn E. Larson, Ravi R. Iyer, Laura Montermini, Massimo Pandolfo, Robert D. Wells
Vydáno 2001Artigo -
14
-
15
Sticky DNA Autor Naoaki Sakamoto, Paul D. Chastain, Paweł Parniewski, Keiichi Ohshima, Massimo Pandolfo, Jack D. Griffith, Robert D. Wells
Vydáno 1999Artigo -
16
Two New Pimelic Diphenylamide HDAC Inhibitors Induce Sustained Frataxin Upregulation in Cells from Friedreich's Ataxia Patients and in a Mouse Model Autor Myriam Rai, Elisabetta Soragni, C. James Chou, Glenn Barnes, Steve Jones, James R. Rusche, Joel Gottesfeld, Massimo Pandolfo
Vydáno 2010Artigo -
17
-
18
-
19
Friedreich ataxia-induced pluripotent stem cell-derived neurons show a cellular phenotype that is corrected by a benzamide HDAC inhibitor Autor Franca Codazzi, Amélie Hu, Myriam Rai, Simona Donatello, Floramarida Salerno Scarzella, Elisabeth Mangiameli, Ilaria Pelizzoni, Fabio Grohovaz, Massimo Pandolfo
Vydáno 2016Artigo -
20
Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Gene Is a Risk Factor of Large-Vessel Atherosclerosis Stroke Autor Shérine Abboud, Pekka J. Karhunen, Dieter Lütjohann, Sirkka Goebeler, Teemu M. Luoto, Silvia Friedrichs, Terho Lehtimäki, Massimo Pandolfo, Reijo Laaksonen
Vydáno 2007Artigo
Vyhledávací nástroje:
Související témata
Medicine
Biology
Ataxia
Neuroscience
Gene
Genetics
Internal medicine
Frataxin
Disease
Iron-binding proteins
Pathology
Psychiatry
Cell biology
Spinocerebellar ataxia
Psychology
Biochemistry
Cerebellum
Endocrinology
Allele
Cohort
Cerebellar ataxia
Genotype
Mitochondrion
Neurodegeneration
Pediatrics
Chemistry
Cohort study
Epilepsy
Molecular biology
Phenotype