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Maps from two interspecific backcross DNA panels available as a community genetic mapping resource

Mammalian genome, 1994-05, Vol.5 (5), p.253-274

1994

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Tissue-specific expression, developmental regulation, and genetic mapping of the gene encoding CCAAT/enhancer binding protein

Genes & development, 1989-08, Vol.3 (8), p.1146-1156

1989

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Spontaneous, heritable colitis in a new substrain of C3H/HeJ mice

Gastroenterology (New York, N.Y. 1943), 1994-12, Vol.107 (6), p.1726-1735

1994

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A Single-Base-Pair Deletion in the β-Glucuronidase Gene Accounts for the Phenotype of Murine Mucopolysaccharidosis Type VII

Proceedings of the National Academy of Sciences - PNAS, 1993-07, Vol.90 (14), p.6567-6571

1993

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Enzyme replacement in murine mucopolysaccharidosis type VII : Neuronal and glial response to β-glucuronidase requires early initiation of enzyme replacement therapy

Pediatric research, 1999-06, Vol.45 (6), p.838-844

1999

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Mutations in a NIMA-Related Kinase Gene, Nek1, Cause Pleiotropic Effects including a Progressive Polycystic Kidney Disease in Mice

Proceedings of the National Academy of Sciences - PNAS, 2000-01, Vol.97 (1), p.217-221

2000

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Genetic Analysis of Susceptibility to Dextran Sulfate Sodium-Induced Colitis in Mice

Genomics (San Diego, Calif.), 1999-01, Vol.55 (2), p.147-156

1999

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Spontaneously colitic C3H/HeJBir mice demonstrate selective antibody reactivity to antigens of the enteric bacterial flora

The Journal of immunology (1950), 1997-07, Vol.159 (1), p.44

1997

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Reversal of pathology in murine mucopolysaccharidosis type VII by somatic cell gene transfer

Nature (London), 1992-12, Vol.360 (6406), p.749-753

1992

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Differential susceptibility of inbred mouse strains to dextran sulfate sodium-induced colitis

American journal of physiology: Gastrointestinal and liver physiology, 1998-03, Vol.274 (3), p.G544-G551

1998

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Murine mucopolysaccharidosis type VII: characterization of a mouse with β-glucuronidase deficiency

The Journal of clinical investigation, 1989-04, Vol.83 (4), p.1258-1266

1989

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Clinical and pathologic findings in two new allelic murine models of polycystic kidney disease

Journal of the American Society of Nephrology, 1999-12, Vol.10 (12), p.2534-2539

1999

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Transgenic Mice Containing Intestinal Fatty Acid-Binding Protein-Human Growth Hormone Fusion Genes Exhibit Correct Regional and Cell-Specific Expression of the Reporter Gene in Their Small Intestine

Proceedings of the National Academy of Sciences - PNAS, 1988-12, Vol.85 (24), p.9611-9615

1988

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Use of Transgenic Mice to Map cis-Acting Elements in the Intestinal Fatty Acid Binding Protein Gene (Fabpi) That Control Its Cell Lineage-Specific and Regional Patterns of Expression along the Duodenal-Colonic and Crypt-Villus Axes of the Gut Epithelium

The Journal of cell biology, 1992-10, Vol.119 (1), p.27-44

1992

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The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationships

The Journal of biological chemistry, 1987-11, Vol.262 (33), p.16060-16071

1987

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CD4+ T cells reactive to enteric bacterial antigens in spontaneously colitic C3H/HeJBir mice: increased T helper cell type 1 response and ability to transfer disease

The Journal of experimental medicine, 1998-03, Vol.187 (6), p.855-864

1998

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Analysis of the tissue-specific expression, developmental regulation, and linkage relationships of a rodent gene encoding heart fatty acid binding protein

The Journal of biological chemistry, 1987-07, Vol.262 (20), p.9709-9717

1987

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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

Pediatric research, 1996-06, Vol.39 (6), p.1050-1054

1996

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Genetic Modifiers of Polycystic Kidney Disease in Intersubspecific KAT2J Mutants

Genomics (San Diego, Calif.), 1999-06, Vol.58 (2), p.129-137

1999

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A murine model of mucopolysaccharidosis VII. Gross and microscopic findings in beta-glucuronidase-deficient mice

The American journal of pathology, 1990-01, Vol.136 (1), p.207-217

1990

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Increased Life Span and Correction of Metabolic Defects in Murine Mucopolysaccharidosis Type VII After Syngeneic Bone Marrow Transplantation

Blood, 1991-12, Vol.78 (11), p.3081-3092

1991

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Mechanisms underlying generation of gradients in gene expression within the intestine: an analysis using transgenic mice containing fatty acid binding protein-human growth hormone fusion genes

Genes & development, 1988-10, Vol.2 (10), p.1318-1332

1988

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The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities

The Journal of biological chemistry, 1989-05, Vol.264 (14), p.7994-8003

1989

Volltextzugriff (PDF)

Enzyme replacement with recombinant β-glucuronidase in the newborn mucopolysaccharidosis type VII mouse

Pediatric research, 1993-12, Vol.34 (6), p.837-840

1993

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Neuropathology of murine mucopolysaccharidosis type VII

Acta neuropathologica, 1996-12, Vol.92 (6), p.562-568

1996

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Maps from two interspecific backcross DNA panels available as a community genetic mapping resource

Tissue-specific expression, developmental regulation, and genetic mapping of the gene encoding CCAAT/enhancer binding protein

Spontaneous, heritable colitis in a new substrain of C3H/HeJ mice

A Single-Base-Pair Deletion in the β-Glucuronidase Gene Accounts for the Phenotype of Murine Mucopolysaccharidosis Type VII

Enzyme replacement in murine mucopolysaccharidosis type VII : Neuronal and glial response to β-glucuronidase requires early initiation of enzyme replacement therapy

Mutations in a NIMA-Related Kinase Gene, Nek1, Cause Pleiotropic Effects including a Progressive Polycystic Kidney Disease in Mice

Genetic Analysis of Susceptibility to Dextran Sulfate Sodium-Induced Colitis in Mice

Spontaneously colitic C3H/HeJBir mice demonstrate selective antibody reactivity to antigens of the enteric bacterial flora

Reversal of pathology in murine mucopolysaccharidosis type VII by somatic cell gene transfer

Differential susceptibility of inbred mouse strains to dextran sulfate sodium-induced colitis

Murine mucopolysaccharidosis type VII: characterization of a mouse with β-glucuronidase deficiency

Clinical and pathologic findings in two new allelic murine models of polycystic kidney disease

Transgenic Mice Containing Intestinal Fatty Acid-Binding Protein-Human Growth Hormone Fusion Genes Exhibit Correct Regional and Cell-Specific Expression of the Reporter Gene in Their Small Intestine

Use of Transgenic Mice to Map cis-Acting Elements in the Intestinal Fatty Acid Binding Protein Gene (Fabpi) That Control Its Cell Lineage-Specific and Regional Patterns of Expression along the Duodenal-Colonic and Crypt-Villus Axes of the Gut Epithelium

The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationships

CD4+ T cells reactive to enteric bacterial antigens in spontaneously colitic C3H/HeJBir mice: increased T helper cell type 1 response and ability to transfer disease

Analysis of the tissue-specific expression, developmental regulation, and linkage relationships of a rodent gene encoding heart fatty acid binding protein

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

Genetic Modifiers of Polycystic Kidney Disease in Intersubspecific KAT2J Mutants

A murine model of mucopolysaccharidosis VII. Gross and microscopic findings in beta-glucuronidase-deficient mice

Increased Life Span and Correction of Metabolic Defects in Murine Mucopolysaccharidosis Type VII After Syngeneic Bone Marrow Transplantation

Mechanisms underlying generation of gradients in gene expression within the intestine: an analysis using transgenic mice containing fatty acid binding protein-human growth hormone fusion genes

The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities

Enzyme replacement with recombinant β-glucuronidase in the newborn mucopolysaccharidosis type VII mouse

Neuropathology of murine mucopolysaccharidosis type VII

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