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Cancer Research|September 20, 2013
Taccalonolide binding to tubulin imparts microtubule stability and potent in vivo activityA L Risinger, J Li, M J Bennett, et al.
Seminars in Perinatology|May 20, 1999
Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complicationsA W Strauss, M J Bennett, P Rinaldo, et al.
AJR. American Journal of Roentgenology|October 1, 1983
Osmotic blood-brain barrier modification: clinical documentation by enhanced CT scanning and/or radionuclide brain scanningE A Neuwelt, H D Specht, J Howieson, et al.
British Journal of Obstetrics and Gynaecology|March 1, 1979
Clinical dilemmas arising from the antenatal diagnosis of neural tube defectsG M Stirrat, A C Turnbull, M J Bennett, et al.
Molecular Ecology|October 24, 2006
The Arabidopsis thaliana/Myzus persicae model system demonstrates that a single gene can influence the interaction between a plant and a sap-feeding insectE J Hunt, J Pritchard, M J Bennett, et al.
Journal of Pediatric Hematology/Oncology|June 11, 1999
Plasma homocysteine levels and folate status in children with sickle cell anemiaH M Rodriguez-Cortes, J C Griener, K Hyland, et al.
The Journal of Pediatrics|February 5, 2000
Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyG M Enns, M J Bennett, C L Hoppel, et al.
American Journal of Medical Genetics|March 17, 1999
Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS)L R Otto, R L Boriack, D J Marsh, et al.
The Veterinary Record|July 8, 1989
Primary hyperoxaluria (L-glyceric aciduria) in the cat: a newly recognised inherited diseaseR E McKerrell, W F Blakemore, M F Heath, et al.
European Journal of Clinical Investigation|July 28, 2001
Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiencyP P Van Veldhoven, E Meyhi, R H Squires, et al.
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