Author

Jan Bijman

Observed names: Bijman, J, Bijman, Jan, J Bijman, J. BIJMAN, J. Bijman, JAN BIJMAN

Institution: Erasmus University Rotterdam

Observed institutions: University of California, Riverside, Goethe University Frankfurt, Radboud University Nijmegen, University of California, Los Angeles, Erasmus MC, Medizinische Hochschule Hannover, Universitätsklinikum Würzburg, Erasmus MC - Sophia Children’s Hospital, Erasmus University Rotterdam

OpenAlex ID: A5109313774

A mouse model for the cystic fibrosis delta F508 mutation.

1995 · J. H. van Doorninck, P. J. French, et al. · The EMBO Journal · 240

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Higher Bioelectric Potentials Due to Decreased Chloride Absorption in the Sweat Glands of Patients with Cystic Fibrosis

1983 · Paul M. Quinton, Jan Bijman · New England Journal of Medicine · 232

Deformation of Network Connectivity in the Inferior Olive of Connexin 36-Deficient Mice Is Compensated by Morphological and Electrophysiological Changes at the Single Neuron Level

2003 · Chris I. De Zeeuw, Edilzh Chorev, et al. · Journal of Neuroscience · 155

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Chloride conductance and genetic background modulate the cystic fibrosis phenotype of ΔF508 homozygous twins and siblings

2001 · Inez Bronsveld, Frauke Mekus, et al. · Journal of Clinical Investigation · 145

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A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.

1996 · P J French, J H van Doorninck, et al. · Journal of Clinical Investigation · 141

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

1995 · Pim J. French, Jan Bijman, et al. · Journal of Biological Chemistry · 138

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

1994 · H J Veeze, D J Halley, et al. · Journal of Clinical Investigation · 133

Categories of ΔF508 homozygous cystic fibrosis twin and sibling pairs with distinct phenotypic characteristics

2000 · Frauke Mekus, Manfred Ballmann, et al. · Twin Research · 123

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

1997 · P. J. French, J. Bijman, et al. · American Journal of Physiology-Cell Physiology · 116

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

1991 · Henk J. Veeze, Maarten Sinaasappel, et al. · Gastroenterology · 112

Influence of abnormal Cl- impermeability on sweating in cystic fibrosis

1984 · J. Bijman, P. M. Quinton · American Journal of Physiology-Cell Physiology · 94

Residual chloride secretion in intestinal tissue of ΔF508 homozygous twins and siblings with cystic fibrosis

2000 · Inez Bronsveld, Frauke Mekus, et al. · Gastroenterology · 91

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Hearing loss in infantile Pompe's disease and determination of underlying pathology in the knockout mouse

2004 · Joep H.J Kamphoven, Martijn M de Ruiter, et al. · Neurobiology of Disease · 62

G-proteins mediate intestinal chloride channel activation

1991 · B C Tilly, M Kansen, et al. · Journal of Biological Chemistry · 55

Cystic-fibrosis-like disease unrelated to the cystic fibrosis transmembrane conductance regulator

1998 · Frauke Mekus, Manfred Ballmann, et al. · Human Genetics · 54

Direct demonstration of high transepithelial chloride-conductance in normal human sweat duct which is absent in cystic fibrosis

1986 · J. Bijman, E. Fr�mter · Pflügers Archiv - European Journal of Physiology · 49

Immortalization of nasal polyp epithelial cells from cystic fibrosis patients

1989 · Bob J. Scholte, Maarten Kansen, et al. · Experimental Cell Research · 47

Electrophysiological studies of forskolin-induced changes in ion transport in the human colon carcinoma cell line HT-29 cl.19A: Lack of evidence for a cAMP-activated basolateral K+ conductance

1991 · R. B. Bajnath, C. Augeron, et al. · The Journal of Membrane Biology · 45

Chronic hypokalaemia of adults: Gitelman's syndrome is frequent but classical Bartter's syndrome is rare

1995 · U. Gladziwa, R. Schwarz, et al. · Nephrology Dialysis Transplantation · 41

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

1987 · Jan Bijman, Paul M Quinton · Pediatric Research · 41

Diversity of the basic defect of homozygous CFTR mutation genotypes in humans

2008 · F Stanke, M Ballmann, et al. · Journal of Medical Genetics · 37

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Immunological localization of cystic fibrosis candidate gene products

1991 · A.T. Hoogeveen, J. Keulemans, et al. · Experimental Cell Research · 37

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

1993 · R. B. Bajnath, J. A. Groot, et al. · Pflügers Archiv - European Journal of Physiology · 35

(Dys)regulation of epithelial chloride channels

1989 · HUGO R. DE JONGE, NINA VAN DEN BERGHE, et al. · Biochemical Society Transactions · 35

Predominantly beta-adrenergic control of equine sweating

1984 · J. Bijman, P. M. Quinton · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · 35

Works count: 65

Citation count: 2,814

H-index: 30

I10-index: 49