J. Bijman

E. Ritz, U. Gladziwa, H. Seyberth, 1995, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Ion transport abnormalities in rectal suction biopsies from children with cystic fibrosis.

H. D. de Jonge, J. Bijman, H. Veeze, 1991, Gastroenterology.

Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype.

D. Halley, H. D. de Jonge, J. Bijman, 1994, The Journal of clinical investigation.

Chloride transport in cultured nasal epithelium of cystic fibrosis patients

B. Scholte, E. Verbeek, J. Bijman, 1990, Pflügers Archiv.

The cystic fibrosis defect approached from different angles — new perspectives on the gene, the chloride channel, diagnosis and therapy

D. Halley, J. Bijman, H. Neijens, 1990, European Journal of Pediatrics.

Ion Transport Regulation in Cystic Fibrosis Epithelia

B. Scholte, J. Bijman, M. Kansen, 1990 .

Characterization of human sweat duct chloride conductance by chloride channel blockers

R. Greger, H. Lang, J. Bijman, 1987, Pflügers Archiv.

Isotype-specific Activation of Cystic Fibrosis Transmembrane Conductance Regulator-Chloride Channels by cGMP-dependent Protein Kinase II (*)

A. Nairn, S. Lohmann, P. French, 1995, The Journal of Biological Chemistry.

X-ray micro-analysis of cultured respiratory epithelial cells from patients with cystic fibrosis.

A. Hoogeveen, J. Bijman, G. Roomans, 1992, Acta physiologica Scandinavica.

Influence of abnormal Cl- impermeability on sweating in cystic fibrosis.

P. Quinton, J. Bijman, 1984, The American journal of physiology.

Value of in vivo electrophysiological measurements to evaluate canine small bowel autotransplants.

F. T. ten Kate, R. Marquet, E. Heineman, 1991, Gut.

The value of in vivo electrophysiological measurements for monitoring functional adaptation after massive small bowel resection in the rat.

R. Marquet, E. Heineman, J. Bijman, 1993, Gut.

Genistein activates CFTR Cl- channels via a tyrosine kinase- and protein phosphatase-independent mechanism.

P. French, B. Scholte, H. D. de Jonge, 1997, The American journal of physiology.

Sequential administration of recombinant human interleukin-2 and dacarbazine in metastatic melanoma. A multicentre phase II study.

S. Rodenhuis, S. Iacobelli, S. Aamdal, 1989, European Journal of Cancer and Clinical Oncology.

In vitro proliferation of primary human head and neck squamous cell carcinomas evaluated by flow cytometry.

P. van den Broek, D. Wagener, J. Bijman, 1987, Cancer letters.

Flow cytometric evaluation of cell dispersion from human head and neck tumors.

P. van den Broek, D. Wagener, J. Bijman, 1985, Cytometry.

Metastatic renal cell cancer treated with low-dose interleukin-2. A phase-II multicentre study.

S. Fosså, C. Rugarli, C. Jasmin, 1989, Cancer treatment reviews.

Flow Cytometric Analysis of Chromosome Damage After Irradiation: Relation to Chromosome Aberrations and Cell Survival

J. Aten, G. Barendsen, J. Kipp, 1984 .

A mouse model for the cystic fibrosis AF 508 mutation

P. French, B. Scholte, E. Verbeek, 2022 .

A mouse model for the cystic fibrosis delta F508 mutation.

H. Morreau, P. French, B. Scholte, 1995, The EMBO journal.

Nucleotide-activated chloride channels in lysosomal membranes.

G. Mancini, R. Bridges, H. D. de Jonge, 1992, Biochemical and biophysical research communications.

Synergistic activation of non-rectifying small-conductance chloride channels by forskolin and phorbol esters in cell-attached patches of the human colon carcinoma cell line HT-29cl.19A

J. Bijman, M. Kansen, J. Groot, 1993, Pflügers Archiv.

CFTR expression and mucin secretion in cultured mouse gallbladder epithelial cells.

W. Colledge, P. French, B. Scholte, 1996, The American journal of physiology.

Calcium ionophore plus excision induce a large conductance chloride channel in membrane patches of human colon carcinoma cells HT-29cl.19A

J. Bijman, M. Kansen, J. Groot, 1993, Experientia.

Lactate and Bicarbonate Uptake in the Sweat Duct of Cystic Fibrosis and Normal Subjects

P. Quinton, J. Bijman, 1987, Pediatric Research.

Regulation of chloride channels in the human colon carcinoma cell line HT29.cl19A

B. Scholte, A. Hoogeveen, J. Bijman, 1993, Pflügers Archiv.

Cultured epithelial cells from patients with cystic fibrosis have an increased expression of the 14 kDa Ca2(+)-binding protein CFA.

H. Galjaard, B. Scholte, A. Hoogeveen, 1991, Biochemical and biophysical research communications.

Immunological localization of cystic fibrosis candidate gene products.

H. Galjaard, R. Willemsen, B. Scholte, 1991, Experimental cell research.

Low-conductance chloride channels in IEC-6 and CF nasal cells expressing CFTR.

M. Wilke, A. Hoogeveen, J. Lecocq, 1993, American Journal of Physiology.

Chloride transport in the cystic fibrosis enterocyte.

D. Halley, B. Scholte, H. D. de Jonge, 1991, Advances in experimental medicine and biology.

Influence of calcium and cyclic nucleotides on beta-adrenergic sweat secretion in equine sweat glands.

P. Quinton, J. Bijman, 1984, The American journal of physiology.

Permeability properties of cell membranes and tight junctions of normal and cystic fibrosis sweat ducts

P. Quinton, J. Bijman, 1987, Pflügers Archiv.