J. Solowska

发表

Quantitative and Functional Analyses of Spastin in the Nervous System: Implications for Hereditary Spastic Paraplegia

B. Himes, Dongyang Huang, S. Brady, 2008, The Journal of Neuroscience.

The microtubule-severing proteins spastin and katanin participate differently in the formation of axonal branches.

L. Qiang, J. Solowska, P. Baas, 2008, Molecular biology of the cell.

Regulation of Microtubule Severing by Katanin Subunits during Neuronal Development

L. Qiang, J. Solowska, P. Baas, 2005, The Journal of Neuroscience.

Hereditary spastic paraplegia SPG4: what is known and not known about the disease.

J. Solowska, P. Baas, 2015, Brain : a journal of neurology.

Evaluation of loss of function as an explanation for SPG4-based hereditary spastic paraplegia.

J. Solowska, P. Baas, J. Garbern, 2010, Human molecular genetics.

Expression of normal and mutant avian integrin subunits in rodent cells [published erratum appears in J Cell Biol 1989 Oct;109(4 Pt 1):1187]

R. Hynes, J. Guan, J. Solowska, 1989, The Journal of cell biology.

Cytoplasmic and transmembrane domains of integrin beta 1 and beta 3 subunits are functionally interchangeable

S. Albelda, J. Solowska, C. Buck, 1991, The Journal of cell biology.

Immunohistochemical and molecular analysis of β1 and β3 integrins

S. Albelda, J. Solowska, L. Damjanovich, 1990 .

Intraspinal Delivery of Neurotrophin-3 Using Neural Stem Cells Genetically Modified by Recombinant Retrovirus

M. Murray, A. Tessler, I. Fischer, 1999, Experimental Neurology.

Axonal Growth Is Sensitive to the Levels of Katanin, a Protein That Severs Microtubules

J. Solowska, P. Baas, D. Baird, 2004, The Journal of Neuroscience.

Truncating mutations of SPAST associated with hereditary spastic paraplegia indicate greater accumulation and toxicity of the M1 isoform of spastin

J. Solowska, P. Baas, Anand N. Rao, 2017, Molecular biology of the cell.

Microtubule-Severing ATPase Spastin in Glioblastoma: Increased Expression in Human Glioblastoma Cell Lines and Inverse Roles in Cell Motility and Proliferation

S. Mörk, J. Janáček, G. Morfini, 2011, Journal of neuropathology and experimental neurology.

Studies on truncating mutations of SPAST associated with Hereditary Spastic Paraplegia indicate greater accumulation and toxicity of the M 1 isoform of spastin Authors

J. Solowska, P. Baas, Anand N. Rao, 2017 .

Pathogenic Mutation of Spastin Has Gain-of-Function Effects on Microtubule Dynamics

M. Davidson, J. Solowska, P. Baas, 2014, The Journal of Neuroscience.

Expression of the mitotic kinesin Kif15 in postmitotic neurons: Implications for neuronal migration and development

J. Solowska, P. Baas, M. Kress, 2003, Journal of neurocytology.

Basic Fibroblast Growth Factor Elicits Formation of Interstitial Axonal Branches via Enhanced Severing of Microtubules

L. Qiang, J. Solowska, P. Baas, 2010, Molecular biology of the cell.

Pontocerebellar Axon Guidance: Neuropilin-1- and Semaphorin 3A-Sensitivity Gradients across Basilar Pontine Nuclei and Semaphorin 3A Variation across Cerebellum

J. Solowska, D. Baird, A. Mazurek, 2002, Molecular and Cellular Neuroscience.

Transplants of cells genetically modified to express neurotrophin‐3 rescue axotomized Clarke's nucleus neurons after spinal cord hemisection in adult rats

A. Tessler, E. Snyder, I. Fischer, 2001, Journal of neuroscience research.

Collapsin-1/Semaphorin-III/D Is Regulated Developmentally in Purkinje Cells and Collapses Pontocerebellar Mossy Fiber Neuronal Growth Cones

S. Rabacchi, J. Solowska, D. Baird, 1999, The Journal of Neuroscience.

Evaluation of loss of function as an explanation for SPG4-based hereditary spastic paraplegia.

J. Solowska, P. Baas, J. Garbern, 2010, Human molecular genetics.