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A variant of GM1 gangliosidosis in a sheep model

Molecular genetics and metabolism, 2018-02, Vol.123 (2), p.S17-S17

Ahern-Rindell, Amelia

2018

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USE OF CRISPR TO VALIDATE CANDIDATE MUTATION IN OVINE GM1 GANGLIOSIDOSIS VARIANT

Molecular genetics and metabolism, 2022-04, Vol.135 (4), p.256-257

2022

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Design and analysis of a CRISPR gene editing strategy in a sheep model variant of GM1 gangliosidosis

Molecular genetics and metabolism, 2019-02, Vol.126 (2), p.S21-S21

2019

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Characterization of a secondary deficiency of neuraminidase activity in a unique ovine model of GM1 gangliosidosis

Molecular genetics and metabolism, 2017-01, Vol.120 (1-2), p.S18

2017

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A size comparison of beta-galactosidase isolated from fibroblasts from normal and GM1-affected sheep

Molecular genetics and metabolism, 2013-02, Vol.108 (2), p.S17-S17

2013

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Bone marrow transplantation in canine GM1 gangliosidosis

Clinical genetics, 1990-10, Vol.38 (4), p.274-280

1990

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2. Characterization of ovine GM1 gangliosidosis using immunofluoresence

Molecular genetics and metabolism, 2008-02, Vol.93 (2), p.14-14

Ahern-Rindell, Amelia

2008

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52 A unique model of GM1 gangliosidosis

Molecular genetics and metabolism, 2007-12, Vol.92 (4), p.23-23

Ahern-Rindell, Amelia

2007

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2. Analysis of beta-galactosidase in an ovine model of GM1-gangliosidosis

Molecular genetics and metabolism, 2009-02, Vol.96 (2), p.S12-S12

2009

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Evaluation of GLB1 In a Novel Ovine Model of GM1-Gangliosidosis

Molecular genetics and metabolism, 2012-02, Vol.105 (2), p.S15-S15

2012

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Evolution

The American biology teacher, 2010-03, Vol.72 (3), p.202-202

Ahern-Rindell, Amelia J.

2010

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Clinical and clinicopathologic characteristics of ovine GM-1 gangliosidosis

Journal of veterinary internal medicine, 1994-05, Vol.8 (3), p.221-223

1994

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3. Comparative analysis of lysosome quantity, size, and location in normal and GM1-affected ovine, canine, and human fibroblasts using fluorescence microscopy

Molecular genetics and metabolism, 2010-02, Vol.99 (2), p.S8

2010

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Vitamin E status and metabolism in adult and aged aryl hydrocarbon receptor null mice

The Journal of nutritional biochemistry, 2010-12, Vol.21 (12), p.1193-1199

2010

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How Do We Know We Are Ready for Comprehensive Change? How Do We Frame Our Vision and Goals?

Transforming Academic Culture and Curriculum, 2024, p.184-192

1, 2024

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Comparison of the canine and human acid β-galactosidase gene

American journal of medical genetics, 1996-05, Vol.63 (2), p.340-345

1996

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Ovine GM-1 gangliosidosis

The American journal of pathology, 1991-12, Vol.139 (6), p.1511-1513

1991

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Applying inquiry-based and cooperative group learning strategies to promote critical thinking

Journal of college science teaching, 1998-12, Vol.28 (3), p.203

Ahern-Rindell, Amelia J

1998

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Applying Inquiry-Based and Cooperative Group Learning Strategies to Promote Critical Thinking: Training Students' Minds and Improving Their Intellect to Become Informed Members of Society

Journal of college science teaching, 1998-12, Vol.28 (3), p.203-207

Ahern-Rindell, Amelia J.

1998

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Prenatal lesions in an ovine fetus with GM1 gangliosidosis

American journal of medical genetics, 1991-04, Vol.39 (1), p.106-111

1991

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Inherited lysosomal storage disease associated with deficiencies of β-galactosidase and α-neuraminidase in sheep

American journal of medical genetics, 1988-09, Vol.31 (1), p.39-56

1988

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Isolation, characterization, and mapping of a human acid beta-galactosidase cDNA

DNA and cell biology, 1990-03, Vol.9 (2), p.119-127

1990

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beta-Galactosidase activity in fibroblasts and tissues from sheep with a lysosomal storage disease

Biochemical genetics, 1988-12, Vol.26 (11-12), p.733-746

1988

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Interspecific genetic complementation analysis of human and sheep fibroblasts with β-galactosidase deficiency

Somatic cell and molecular genetics, 1989-11, Vol.15 (6), p.525-533

1989

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The genetic and biochemical characterization of an inherited ovine lysosomal storage disease

Ahern-Rindell, Amelia Julia

1988

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A variant of GM1 gangliosidosis in a sheep model

USE OF CRISPR TO VALIDATE CANDIDATE MUTATION IN OVINE GM1 GANGLIOSIDOSIS VARIANT

Design and analysis of a CRISPR gene editing strategy in a sheep model variant of GM1 gangliosidosis

Characterization of a secondary deficiency of neuraminidase activity in a unique ovine model of GM1 gangliosidosis

A size comparison of beta-galactosidase isolated from fibroblasts from normal and GM1-affected sheep

Bone marrow transplantation in canine GM1 gangliosidosis

2. Characterization of ovine GM1 gangliosidosis using immunofluoresence

52 A unique model of GM1 gangliosidosis

2. Analysis of beta-galactosidase in an ovine model of GM1-gangliosidosis

Evaluation of GLB1 In a Novel Ovine Model of GM1-Gangliosidosis

Evolution

Clinical and clinicopathologic characteristics of ovine GM-1 gangliosidosis

3. Comparative analysis of lysosome quantity, size, and location in normal and GM1-affected ovine, canine, and human fibroblasts using fluorescence microscopy

Vitamin E status and metabolism in adult and aged aryl hydrocarbon receptor null mice

How Do We Know We Are Ready for Comprehensive Change? How Do We Frame Our Vision and Goals?

Comparison of the canine and human acid β-galactosidase gene

Ovine GM-1 gangliosidosis

Applying inquiry-based and cooperative group learning strategies to promote critical thinking

Applying Inquiry-Based and Cooperative Group Learning Strategies to Promote Critical Thinking: Training Students' Minds and Improving Their Intellect to Become Informed Members of Society

Prenatal lesions in an ovine fetus with GM1 gangliosidosis

Inherited lysosomal storage disease associated with deficiencies of β-galactosidase and α-neuraminidase in sheep

Isolation, characterization, and mapping of a human acid beta-galactosidase cDNA

beta-Galactosidase activity in fibroblasts and tissues from sheep with a lysosomal storage disease

Interspecific genetic complementation analysis of human and sheep fibroblasts with β-galactosidase deficiency

The genetic and biochemical characterization of an inherited ovine lysosomal storage disease

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