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Cytogenetics and Cell Genetics|January 1, 1994
The human gene for water channel aquaporin 1 (AQP1) is localized on chromosome 7p15-->p14P M Deen, D O Weghuis, A Geurs van Kessel, et al.
Kidney International|February 1, 1993
Effect of protein kinase C activation and down-regulation on active calcium transportR J Bindels, J A Dempster, P L Ramakers, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 24, 2001
DNA repair gene XRCC1 polymorphisms, smoking, and bladder cancer riskM C Stern, D M Umbach, C H van Gils, et al.
Chemical Communications (Cambridge, England)|January 23, 2019
Photoenzymatic epoxidation of styrenesMorten M C H van Schie, Caroline E Paul, Isabel W C E Arends, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 27, 2014
Association between levator hiatal dimensions on ultrasound during first pregnancy and mode of deliveryG A van Veelen, K J Schweitzer, N E van Hoogenhuijze, et al.
Developmental Biology|December 1, 1989
The initiation of hepatocyte-specific gene expression within embryonic hepatocytes is a stochastic eventM A van Roon, J A Aten, C H van Oven, et al.
The Journal of Biological Chemistry|June 15, 1989
Inhibition of inositol 1,4,5-trisphosphate-induced Ca2+ release in permeabilized pancreatic acinar cells by hormonal and phorbol ester pretreatmentP H Willems, B A Van den Broek, C H Van Os, et al.
Cancer Research|April 1, 1985
Peanut agglutinin, a marker for T-cell acute lymphoblastic leukemia with a good prognosisA J Veerman, P H Hogeman, D R Huismans, et al.
Alimentary Pharmacology & Therapeutics|June 26, 1999
The effect of Helicobacter pylori eradication on intragastric pH during dosing with lansoprazole or ranitidineM A van Herwaarden, M Samsom, C H van Nispen, et al.
The Journal of Pediatrics|March 4, 2000
Carbohydrate-deficient glycoprotein syndrome type 1a: a variant phenotype with borderline cognitive dysfunction, cerebellar hypoplasia, and coagulation disturbancesC H van Ommen, M Peters, P G Barth, et al.
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