N. Galvin

发表

Overcoming the blood-brain barrier with high-dose enzyme replacement therapy in murine mucopolysaccharidosis VII.

W. Sly, J. Grubb, C. Vogler, 2005, Proceedings of the National Academy of Sciences of the United States of America.

In Vitro Processing of Aleurain, a Barley Vacuolar Thiol Protease.

T. Baranski, J. Rogers, N. Galvin, 1990, The Plant cell.

Early fetal development of lung vasculature.

D. Sawyer, D. Demello, L. Reid, 1997, American journal of respiratory cell and molecular biology.

Electrocardiographic and other cardiac anomalies in beta-glucuronidase-null mice corrected by nonablative neonatal marrow transplantation.

M. Lessard, A. Schuldt, C. Vogler, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Repetitive Self-Limited Acute Pancreatitis Induces Pancreatic Fibrogenesis in the Mouse

B. Neuschwander‐Tetri, J. Poulos, R. Britton, 2000, Digestive Diseases and Sciences.

Enzyme therapy in mannose receptor-null mucopolysaccharidosis VII mice defines roles for the mannose 6-phosphate and mannose receptors

W. Sly, J. Grubb, S. Tomatsu, 2006, Proceedings of the National Academy of Sciences.

Monoclonal antibodies that recognize calcium-dependent structures of human thrombospondin. Characterization and mapping of their epitopes.

V. Dixit, K. O'rourke, W. Frazier, 1986, The Journal of biological chemistry.

Mapping of epitopes for monoclonal antibodies against human platelet thrombospondin with electron microscopy and high sensitivity amino acid sequencing

V. Dixit, S. Santoro, K. O'rourke, 1985, The Journal of cell biology.

Treatment of murine mucopolysaccharidosis type VII by syngeneic bone marrow transplantation in neonates.

W. Sly, M. Sands, B. Gwynn, 1993, Laboratory investigation; a journal of technical methods and pathology.

Chemically modified β-glucuronidase crosses blood–brain barrier and clears neuronal storage in murine mucopolysaccharidosis VII

W. Sly, J. Grubb, C. Vogler, 2008, Proceedings of the National Academy of Sciences.

Murine Mucopolysaccharidosis VII: Impact of Therapies on the Phenotype, Clinical Course, and Pathology in a Model of a Lysosomal Storage Disease

W. Sly, M. Sands, C. Vogler, 2001, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Association of the cyclic AMP chemotaxis receptor with the detergent- insoluble cytoskeleton of Dictyostelium discoideum

W. Frazier, N. Galvin, D. Stockhausen, 1984, The Journal of cell biology.

Transgene produces massive overexpression of human β-glucuronidase in mice, lysosomal storage of enzyme, and strain-dependent tumors

W. Sly, X. Zhou, C. Vogler, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Murine mucopolysaccharidosis type VII: The impact of therapies on the clinical course and pathology in a murine model of lysosomal storage disease

W. Sly, M. Sands, C. Vogler, 1998, Journal of Inherited Metabolic Disease.

Enzyme replacement therapy for murine mucopolysaccharidosis type VII.

W. Sly, J. Grubb, M. Sands, 1994, The Journal of clinical investigation.

Cloning and sequence analysis of murine cytomegalovirus protease and capsid assembly protein genes.

J. Loutsch, N. Galvin, B. Holwerda, 1994, Biochemical and biophysical research communications.

Attenuation of murine lysosomal storage disease by allogeneic neonatal bone marrow transplantation using costimulatory blockade and donor lymphocyte infusion without myeloablation.

M. Lessard, J. Proctor, B. Soper, 2006, Clinical immunology.

Ultrastructural and immunocytochemical evidence for the presence of polarised plasma membrane H(+)-ATPase in two specialised cell types in the chick embryo chorioallantoic membrane.

D. Levine, R. Narbaitz, N. Galvin, 1995, Journal of anatomy.

Intravitreal Gene Therapy Reduces Lysosomal Storage in Specific Areas of the CNS in Mucopolysaccharidosis VII Mice

M. Sands, S. Bassnett, J. Ogilvie, 2003, The Journal of Neuroscience.

Retinal function is improved in a murine model of a lysosomal storage disease following bone marrow transplantation.

M. Sands, C. Vogler, N. Galvin, 2000, Experimental eye research.

Enzyme Replacement with Recombinant β-Glucuronidase in Murine Mucopolysaccharidosis Type VII: Impact of Therapy during the First Six Weeks of Life on Subsequent Lysosomal Storage, Growth, and Survival

W. Sly, M. Sands, E. Birkenmeier, 1996, Pediatric Research.

Enzyme Replacement in Murine Mucopolysaccharidosis Type VII: Neuronal and Glial Response to β-Glucuronidase Requires Early Initiation of Enzyme Replacement Therapy

W. Sly, J. Baty, M. Sands, 1999, Pediatric Research.

Chemotactic Transduction in the Cellular Slime Molds

W. Frazier, N. Galvin, B. L. Meyers-Hutchins, 1984 .

Intracellular localization and unique conserved sequences of three small nucleolar RNAs.

J. Brown, N. Selvamurugan, N. Galvin, 1997, Nucleic acids research.

A Murine Model of Infantile Neuronal Ceroid Lipofuscinosis—Ultrastructural Evaluation of Storage in the Central Nervous System and Viscera

M. Sands, A. Kovács, C. Vogler, 2008, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Neuropathology of murine mucopolysaccharidosis type VII

W. Sly, E. Birkenmeier, C. Vogler, 1996, Acta Neuropathologica.

ehavioral o bservations of a unique Xanthic colony of p elagic Sea Snakes, Pelamis platurus, residing in Golfo dc osta r ica

N. Galvin, Phoenix Zoo, 2012 .

First report of Vesper rat, Nyctomys sumicrasti (Rodentia: Muridae) feeding on Palm fruits

N. Galvin, Phoenix Zoo, J. Corrigan, 2009 .

Detection of elemental mercury in abdominal wall soft tissue

A. Scalzo, M. Mullins, N. Galvin, 2009, Journal of Medical Toxicology.

Interaction of human thrombospondin with types I-V collagen: direct binding and electron microscopy

V. Dixit, V M Dixit, P. Vance, 1987, The Journal of cell biology.

Pathology of the ear in murine mucopolysaccharidosis type VII. Morphologic correlates of hearing loss.

W. Sly, E. Birkenmeier, C. Vogler, 1994, Laboratory investigation; a journal of technical methods and pathology.

A Novel Model of Murine Mucopolysaccharidosis Type VII due to an Intracisternal A Particle Element Transposition into the β-Glucuronidase Gene: Clinical and Pathologic Findings

W. Sly, M. Sands, E. Birkenmeier, 2001, Pediatric Research.

Early Onset of Lysosomal Storage Disease in a Murine Model of Mucopolysaccharidosis Type VII: Undegraded Substrate Accumulates in Many Tissues in the Fetus and Very Young MPS VII Mouse

B. Soper, C. Vogler, B. Levy, 2005, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Mapping Functional Domains of Human Platelet Thrombospondin with Electro-Blotting and High Sensitivity Sequencing

V. Dixit, S. Santoro, K. O'rourke, 1987 .

Physiological and morphological evidence for coupling in mouse salivary gland acinar cells

S. B. Kater, N. Galvin, 1978, The Journal of cell biology.

The mode of termination of the hypothalamic projection to the dentate gyrus: An EM autoradiographic study

W. Cowan, B. Stanfield, N. Galvin, 1983, Brain Research.

Discoidin I-membrane interactions II. Discoidin I binds to and agglutinates negatively charged phospholipid vesicles

W. Frazier, N. Galvin, J. Bartles, 1982 .

Degenerative changes in epinephrine tonic vasomotor neurons in Alzheimer's disease

W. Burke, R. Nixon, K. Gillespie, 1994, Brain Research.

Lysosomal Storage Disease : Diagnosis and Role of Animal Models in Evaluation of Treatment

N. Galvin, 2008 .