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Transgenic rescue of Krabbe disease in the twitcher mouse

Gene therapy, 2004-08, Vol.11 (15), p.1188-1194

2004

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BAC and PAC DNA for the Generation of Transgenic Animals

BioTechniques, 2002-07, Vol.33 (1), p.51-53

2002

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Stereological assessment of immunohistochemical markers in the auditory nuclei of bottlenose dolphins

Journal of comparative pathology, 2023-05, Vol.203, p.68-68

2023

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Altered Ultrasonic Vocalization in Mice with a Disruption in the Foxp2 Gene

Proceedings of the National Academy of Sciences - PNAS, 2005-07, Vol.102 (27), p.9643-9648

2005

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Identification and characterization of novel mutations of the aspartoacylase gene in non‐Jewish patients with Canavan disease

Journal of inherited metabolic disease, 2002-11, Vol.25 (7), p.557-570

2002

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Molecular heterogeneity of late-onset forms of globoid-cell leukodystrophy

American journal of human genetics, 1996-12, Vol.59 (6), p.1233-1242

1996

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Entorhinal cortex lesioning promotes neurogenesis in the hippocampus of adult mice

Neuroscience, 2004, Vol.127 (4), p.881-891

2004

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CR leads in cardiac emergencies. A preliminary study

Chest, 1991-04, Vol.99 (4), p.904-910

1991

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Digitized cardiac potentials recorded with CR leads. Development of a portable electrocardiograph

Chest, 1991-11, Vol.100 (5), p.1364-1370

1991

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Interactions of primary neuroepithelial progenitor and brain endothelial cells: distinct effect on neural progenitor maintenance and differentiation by soluble factors and direct contact

Cell research, 2007-07, Vol.17 (7), p.619-626

2007

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Kinetics of the T-cell receptor CD4 and CD8 Vβ repertoire in HIV-1 vertically infected infants early treated with HAART

AIDS (London), 2001-11, Vol.15 (16), p.2075-2084

2001

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Selective expression of presenilin 1 in neural progenitor cells rescues the cerebral hemorrhages and cortical lamination defects in presenilin 1-null mutant mice

Development (Cambridge), 2005-09, Vol.132 (17), p.3873-3883

2005

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The substrate-specificity of human lysosomal alpha-D-mannosidase in relation to genetic alpha-mannosidosis

Biochemical journal, 1991-08, Vol.277 ( Pt 3) (3), p.743-751

1991

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Antisulfatide IgG antibodies recognize HIV proteins

Journal of acquired immune deficiency syndromes and human retrovirology, 1997-05, Vol.15 (1), p.83-84

1997

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Substrate specificity of the bovine and feline neutral α-mannosidases

Biochemical journal, 1992-08, Vol.286 (1), p.55-63

1992

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A human lysosomal alpha-mannosidase specific for the core of complex glycans

The Journal of biological chemistry, 1992-05, Vol.267 (14), p.9706-9712

1992

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Neural progenitor cells do not differentiate prematurely in presenilin-1 null mutant mice

Neuroscience letters, 2004-11, Vol.371 (2), p.249-254

2004

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Substrate specificity of human liver neutral α-mannosidase

Biochemical journal, 1992-08, Vol.286 (1), p.47-53

1992

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Modifications of Ganglioside Patterns in Human Meningiomas

Journal of neurochemistry, 1983-03, Vol.40 (3), p.777-782

1983

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Comparison of digitized ECGs simultaneously recorded with CR and V leads

Journal of electrocardiology, 1995-10, Vol.28 (4), p.287-295

1995

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Molecular basis of late-life globoid cell leukodystrophy

Human mutation, 1999, Vol.14 (3), p.256-262

1999

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Correction of the Galactocerebrosidase Deficiency in Globoid Cell Leukodystrophy-Cultured Cells by SL3-3 Retroviral-Mediated Gene Transfer

Biochemical and biophysical research communications, 1996-01, Vol.218 (3), p.766-771

1996

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A Human Kidney cDNA Which Induces a Cell Surface Protein Epitope Recognized by a Monoclonal Antibody against Galactosylceramide

Biochemical and biophysical research communications, 1996-10, Vol.227 (2), p.636-641

1996

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Late-onset G sub M2 gangliosidosis: Ashkenazi Jewish family with an exon 5 mutation (Tyr sup 180 right arrow His) in the Hex A alpha-chain gene

Neurology, 1996-08, Vol.47 (2), p.547-552

1996

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Transgenic rescue of Krabbe disease in the twitcher mouse

Brain and blood biomarkers of tauopathy and neuronal injury in humans and rats with neurobehavioral syndromes following blast exposure

BAC and PAC DNA for the Generation of Transgenic Animals

Stereological assessment of immunohistochemical markers in the auditory nuclei of bottlenose dolphins

Altered Ultrasonic Vocalization in Mice with a Disruption in the Foxp2 Gene

Identification and characterization of novel mutations of the aspartoacylase gene in non‐Jewish patients with Canavan disease

Molecular heterogeneity of late-onset forms of globoid-cell leukodystrophy

Entorhinal cortex lesioning promotes neurogenesis in the hippocampus of adult mice

CR leads in cardiac emergencies. A preliminary study

Digitized cardiac potentials recorded with CR leads. Development of a portable electrocardiograph

Interactions of primary neuroepithelial progenitor and brain endothelial cells: distinct effect on neural progenitor maintenance and differentiation by soluble factors and direct contact

Kinetics of the T-cell receptor CD4 and CD8 Vβ repertoire in HIV-1 vertically infected infants early treated with HAART

Selective expression of presenilin 1 in neural progenitor cells rescues the cerebral hemorrhages and cortical lamination defects in presenilin 1-null mutant mice

The substrate-specificity of human lysosomal alpha-D-mannosidase in relation to genetic alpha-mannosidosis

Antisulfatide IgG antibodies recognize HIV proteins

Substrate specificity of the bovine and feline neutral α-mannosidases

A human lysosomal alpha-mannosidase specific for the core of complex glycans

Neural progenitor cells do not differentiate prematurely in presenilin-1 null mutant mice

Substrate specificity of human liver neutral α-mannosidase

Modifications of Ganglioside Patterns in Human Meningiomas

Comparison of digitized ECGs simultaneously recorded with CR and V leads

Molecular basis of late-life globoid cell leukodystrophy

Correction of the Galactocerebrosidase Deficiency in Globoid Cell Leukodystrophy-Cultured Cells by SL3-3 Retroviral-Mediated Gene Transfer

A Human Kidney cDNA Which Induces a Cell Surface Protein Epitope Recognized by a Monoclonal Antibody against Galactosylceramide

Late-onset G sub M2 gangliosidosis: Ashkenazi Jewish family with an exon 5 mutation (Tyr sup 180 right arrow His) in the Hex A alpha-chain gene

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