A. Matilla

发表

Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress

A. Lees, T. Révész, N. Wood, 2006, Journal of neurochemistry.

The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1

H. Zoghbi, H. Orr, T. Isobe, 1997, Nature.

Thecerebellar leucine-rich acidic nuclear protein interactswithataxin-1

H. Orr, U. Stäubli, T. Isobe, 2022 .

Mice Lacking Ataxin-1 Display Learning Deficits and Decreased Hippocampal Paired-Pulse Facilitation

H. Zoghbi, J. Sweatt, H. Orr, 1998, The Journal of Neuroscience.

Mapmodulin/Leucine-rich Acidic Nuclear Protein Binds the Light Chain of Microtubule-associated Protein 1B and Modulates Neuritogenesis*

H. Zoghbi, H. Orr, Jesús García, 2003, Journal of Biological Chemistry.

Purkinje Cell Expression of a Mutant Allele of SCA1in Transgenic Mice Leads to Disparate Effects on Motor Behaviors, Followed by a Progressive Cerebellar Dysfunction and Histological Alterations

H. Zoghbi, H. Orr, E. Burright, 1997, The Journal of Neuroscience.

Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p

M. Leppert, H. Zoghbi, K. Digre, 1995, Nature Genetics.

Association of ataxin-7 with the proteasome subunit S4 of the 19S regulatory complex.

C. van Broeckhoven, C. Gorbea, L. Ptáček, 2001, Human molecular genetics.

The Anp32 family of proteins containing leucine-rich repeats

M. Radrizzani, A. Matilla, 2008, The Cerebellum.

Anp32e/Cpd1 regulates protein phosphatase 2A activity at synapses during synaptogenesis

M. Radrizzani, H. Carminatti, C. Perandones, 2006, The European journal of neuroscience.

t(3;14)(q26;q11) associated with megakaryoblastic transformation of chronic myeloid leukemia.

F. Solé, A. Matilla, R. A. de la Chica, 1991, Cancer genetics and cytogenetics.