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Gut Microbiota Regulate Pancreatic Growth, Exocrine Function, and Gut Hormones

Diabetes (New York, N.Y.), 2022-05, Vol.71 (5), p.945-960

2022

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Ear2 deletion causes early memory and learning deficits in APP/PS1 mice

The Journal of neuroscience, 2014-06, Vol.34 (26), p.8845-8854

2014

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Participation of Autophagy in Storage of Lysosomes in Neurons from Mouse Models of Neuronal Ceroid-Lipofuscinoses (Batten Disease)

The American journal of pathology, 2005-12, Vol.167 (6), p.1713-1728

2005

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Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity

Biochemical journal, 2006-11, Vol.400 (1), p.63-73

2006

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Disturbed cholesterol traffic but normal proteolytic function in LAMP-1/LAMP-2 double-deficient fibroblasts

Molecular biology of the cell, 2004-07, Vol.15 (7), p.3132-3145

2004

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Involvement of two different cell death pathways in retinal atrophy of cathepsin D-deficient mice

Molecular and cellular neuroscience, 2003-02, Vol.22 (2), p.146-161

2003

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Mice deficient for the lysosomal proteinase cathepsin D exhibit progressive atrophy of the intestinal mucosa and profound destruction of lymphoid cells

The EMBO journal, 1995-08, Vol.14 (15), p.3599-3608

1995

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Mannose 6-phosphate receptors, Niemann-Pick C2 protein, and lysosomal cholesterol accumulation

Journal of lipid research, 2005-12, Vol.46 (12), p.2559-2569

2005

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LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice

Human molecular genetics, 2003-03, Vol.12 (6), p.631-646

2003

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Cathepsin D Deficiency Induces Lysosomal Storage with Ceroid Lipofuscin in Mouse CNS Neurons

The Journal of neuroscience, 2000-09, Vol.20 (18), p.6898-6906

2000

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Golgi GDP-fucose Transporter-deficient Mice Mimic Congenital Disorder of Glycosylation IIc/Leukocyte Adhesion Deficiency II

The Journal of biological chemistry, 2007-04, Vol.282 (14), p.10762-10772

2007

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Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling

The FASEB journal, 2000-10, Vol.14 (13), p.2075-2086

2000

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The Normal Phenotype of Pmm1-Deficient Mice Suggests that Pmm1 Is Not Essential for Normal Mouse Development

Molecular and Cellular Biology, 2006-08, Vol.26 (15), p.5621-5635

2006

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Involvement of Nitric Oxide Released from Microglia-Macrophages in Pathological Changes of Cathepsin D-Deficient Mice

The Journal of neuroscience, 2001-10, Vol.21 (19), p.7526-7533

2001

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Efficacy of enzyme replacement therapy in α-mannosidosis mice: a preclinical animal study

Human molecular genetics, 2004-09, Vol.13 (18), p.1979-1988

2004

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Phenotype of Arylsulfatase A-Deficient Mice: Relationship to Human Metachromatic Leukodystrophy

Proceedings of the National Academy of Sciences - PNAS, 1996-12, Vol.93 (25), p.14821-14826

1996

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Autophagic vacuoles with sarcolemmal features delineate danon disease and related myopathies

Journal of neuropathology and experimental neurology, 2005-06, Vol.64 (6), p.513-522

2005

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Granzyme-mediated Cytotoxicity Does Not Involve the Mannose 6-Phosphate Receptors on Target Cells

The Journal of biological chemistry, 2004-05, Vol.279 (19), p.20200-20210

2004

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Involvement of Cathepsin E in Exogenous Antigen Processing in Primary Cultured Murine Microglia

The Journal of biological chemistry, 2002-02, Vol.277 (7), p.4816-4822

2002

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Early embryonic death of mice deficient in gamma-adaptin

The Journal of biological chemistry, 1999-02, Vol.274 (9), p.5385-5390

1999

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Proteolytic degradation of glutamate decarboxylase mediates disinhibition of hippocampal CA3 pyramidal cells in cathepsin D‐deficient mice

Journal of neurochemistry, 2005-08, Vol.94 (3), p.680-690

2005

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Targeted Disruption of the Arylsulfatase B Gene Results in Mice Resembling the Phenotype of Mucopolysaccharidosis VI

Proceedings of the National Academy of Sciences - PNAS, 1996-08, Vol.93 (16), p.8214-8219

1996

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Amyloidogenic Processing of Human Amyloid Precursor Protein in Hippocampal Neurons Devoid of Cathepsin D

The Journal of biological chemistry, 1996-11, Vol.271 (44), p.27241-27244

1996

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Mu 1A deficiency induces a profound increase in MPR300/IGF-II receptor internalization rate

Journal of cell science, 2001-12, Vol.114 (Pt 24), p.4469-4476

2001

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Mice Deficient in Lysosomal Acid Phosphatase Develop Lysosomal Storage in the Kidney and Central Nervous System

The Journal of biological chemistry, 1997-07, Vol.272 (30), p.18628-18635

1997

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Gut Microbiota Regulate Pancreatic Growth, Exocrine Function, and Gut Hormones

Ear2 deletion causes early memory and learning deficits in APP/PS1 mice

Participation of Autophagy in Storage of Lysosomes in Neurons from Mouse Models of Neuronal Ceroid-Lipofuscinoses (Batten Disease)

Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity

Disturbed cholesterol traffic but normal proteolytic function in LAMP-1/LAMP-2 double-deficient fibroblasts

Involvement of two different cell death pathways in retinal atrophy of cathepsin D-deficient mice

Mice deficient for the lysosomal proteinase cathepsin D exhibit progressive atrophy of the intestinal mucosa and profound destruction of lymphoid cells

Mannose 6-phosphate receptors, Niemann-Pick C2 protein, and lysosomal cholesterol accumulation

LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice

Cathepsin D Deficiency Induces Lysosomal Storage with Ceroid Lipofuscin in Mouse CNS Neurons

Golgi GDP-fucose Transporter-deficient Mice Mimic Congenital Disorder of Glycosylation IIc/Leukocyte Adhesion Deficiency II

Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling

The Normal Phenotype of Pmm1-Deficient Mice Suggests that Pmm1 Is Not Essential for Normal Mouse Development

Involvement of Nitric Oxide Released from Microglia-Macrophages in Pathological Changes of Cathepsin D-Deficient Mice

Efficacy of enzyme replacement therapy in α-mannosidosis mice: a preclinical animal study

Phenotype of Arylsulfatase A-Deficient Mice: Relationship to Human Metachromatic Leukodystrophy

Autophagic vacuoles with sarcolemmal features delineate danon disease and related myopathies

Granzyme-mediated Cytotoxicity Does Not Involve the Mannose 6-Phosphate Receptors on Target Cells

Involvement of Cathepsin E in Exogenous Antigen Processing in Primary Cultured Murine Microglia

Early embryonic death of mice deficient in gamma-adaptin

Proteolytic degradation of glutamate decarboxylase mediates disinhibition of hippocampal CA3 pyramidal cells in cathepsin D‐deficient mice

Targeted Disruption of the Arylsulfatase B Gene Results in Mice Resembling the Phenotype of Mucopolysaccharidosis VI

Amyloidogenic Processing of Human Amyloid Precursor Protein in Hippocampal Neurons Devoid of Cathepsin D

Mu 1A deficiency induces a profound increase in MPR300/IGF-II receptor internalization rate

Mice Deficient in Lysosomal Acid Phosphatase Develop Lysosomal Storage in the Kidney and Central Nervous System

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