de Jonge H - Search Results

1

Subcellular distribution of CFTR in rat intestine supports a physiologic role for CFTR regulation by vesicle traffic.

Ameen NA, van Donselaar E, Posthuma G, de Jonge H, McLaughlin G, Geuze HJ, Marino C, Peters PJ. Ameen NA, et al. Among authors: de jonge h. Histochem Cell Biol. 2000 Sep;114(3):219-28. doi: 10.1007/s004180000167. Histochem Cell Biol. 2000. PMID: 11083465

2

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

French PJ, van Doorninck JH, Peters RH, Verbeek E, Ameen NA, Marino CR, de Jonge HR, Bijman J, Scholte BJ. French PJ, et al. Among authors: de jonge hr. J Clin Invest. 1996 Sep 15;98(6):1304-12. doi: 10.1172/JCI118917. J Clin Invest. 1996. PMID: 8823295 Free PMC article.

3

Expression and regulation of chloride channels in neonatal rat cardiomyocytes.

Tilly BC, Bezstarosti K, Boomaars WE, Marino CR, Lamers JM, de Jonge HR. Tilly BC, et al. Among authors: de jonge hr. Mol Cell Biochem. 1996 Apr 12-26;157(1-2):129-35. doi: 10.1007/BF00227891. Mol Cell Biochem. 1996. PMID: 8739239

4

Biochemical methods to assess CFTR expression and membrane localization.

Farinha CM, Penque D, Roxo-Rosa M, Lukacs G, Dormer R, McPherson M, Pereira M, Bot AG, Jorna H, Willemsen R, Dejonge H, Heda GD, Marino CR, Fanen P, Hinzpeter A, Lipecka J, Fritsch J, Gentzsch M, Edelman A, Amaral MD. Farinha CM, et al. J Cyst Fibros. 2004 Aug;3 Suppl 2:73-7. doi: 10.1016/j.jcf.2004.05.017. J Cyst Fibros. 2004. PMID: 15463932 Free article.

5

Applicability of different antibodies for immunohistochemical localization of CFTR in sweat glands from healthy controls and from patients with cystic fibrosis.

Claass A, Sommer M, de Jonge H, Kälin N, Tümmler B. Claass A, et al. Among authors: de jonge h. J Histochem Cytochem. 2000 Jun;48(6):831-7. doi: 10.1177/002215540004800611. J Histochem Cytochem. 2000. PMID: 10820156

6

Regulated trafficking of the CFTR chloride channel.

Kleizen B, Braakman I, de Jonge HR. Kleizen B, et al. Among authors: de jonge hr. Eur J Cell Biol. 2000 Aug;79(8):544-56. doi: 10.1078/0171-9335-00078. Eur J Cell Biol. 2000. PMID: 11001491 Review.

7

Folding of CFTR is predominantly cotranslational.

Kleizen B, van Vlijmen T, de Jonge HR, Braakman I. Kleizen B, et al. Mol Cell. 2005 Oct 28;20(2):277-87. doi: 10.1016/j.molcel.2005.09.007. Mol Cell. 2005. PMID: 16246729 Free article.

8

Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings.

Bronsveld I, Mekus F, Bijman J, Ballmann M, de Jonge HR, Laabs U, Halley DJ, Ellemunter H, Mastella G, Thomas S, Veeze HJ, Tümmler B. Bronsveld I, et al. Among authors: de jonge hr. J Clin Invest. 2001 Dec;108(11):1705-15. doi: 10.1172/JCI12108. J Clin Invest. 2001. PMID: 11733566 Free PMC article.

9

Bioelectric characterization of epithelia from neonatal CFTR knockout ferrets.

Fisher JT, Tyler SR, Zhang Y, Lee BJ, Liu X, Sun X, Sui H, Liang B, Luo M, Xie W, Yi Y, Zhou W, Song Y, Keiser N, Wang K, de Jonge HR, Engelhardt JF. Fisher JT, et al. Among authors: de jonge hr. Am J Respir Cell Mol Biol. 2013 Nov;49(5):837-44. doi: 10.1165/rcmb.2012-0433OC. Am J Respir Cell Mol Biol. 2013. PMID: 23782101 Free PMC article.

10

In vivo measurement of chloride and water secretion in the jejunum of cystic fibrosis patients.

Teune TM, Timmers-Reker AJ, Bouquet J, Bijman J, De Jonge HR, Sinaasappel M. Teune TM, et al. Among authors: de jonge hr. Pediatr Res. 1996 Oct;40(4):522-7. doi: 10.1203/00006450-199610000-00002. Pediatr Res. 1996. PMID: 8888277

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