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Publication

Production and characterization of murine models of classic and intermediate maple syrup urine disease.

Gregg E Homanics | Kristen Skvorak | Carolyn Ferguson | Simon Watkins | Harbhajan S Paul
BMC medical genetics | 2006

Maple Syrup Urine Disease (MSUD) is an inborn error of metabolism caused by a deficiency of branched-chain keto acid dehydrogenase. MSUD has several clinical phenotypes depending on the degree of enzyme deficiency. Current treatments are not satisfactory and require new approaches to combat this disease. A major hurdle in developing new treatments has been the lack of a suitable animal model.

Pubmed ID: 16579849

Research resources used in this publication

None found

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Antibodies used in this publication

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Associated grants

  • Agency: NIAAA NIH HHS, United States
    Id: R37 AA010422
  • Agency: NIDDK NIH HHS, United States
    Id: DK51960
  • Agency: NIAAA NIH HHS, United States
    Id: AA10422
  • Agency: NIDDK NIH HHS, United States
    Id: DK57956
  • Agency: NIDDK NIH HHS, United States
    Id: DK57386
  • Agency: NIAAA NIH HHS, United States
    Id: R01 AA010422

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This is a list of tools and resources that we have found mentioned in this publication.

129/SvEv (tool)

RRID:MGI:5653381

laboratory mouse with name 129/SvEv from MGI.

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C57BL/6J (tool)

RRID:IMSR_JAX:000664

Mus musculus with name C57BL/6J from IMSR.

View all literature mentions

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