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Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.
Stanke F, Ballmann M, Bronsveld I, Dörk T, Gallati S, Laabs U, Derichs N, Ritzka M, Posselt HG, Harms HK, Griese M, Blau H, Mastella G, Bijman J, Veeze H, Tümmler B. Stanke F, et al. Among authors: bijman j. J Med Genet. 2008 Jan;45(1):47-54. doi: 10.1136/jmg.2007.053561. J Med Genet. 2008. PMID: 18178635 Free article.
Cystic fibrosis transmembrane conductance regulator (CFTR)-mediated residual chloride secretion does not protect against early chronic Pseudomonas aeruginosa infection in F508del homozygous cystic fibrosis patients.
Derichs N, Mekus F, Bronsveld I, Bijman J, Veeze HJ, von der Hardt H, Tummler B, Ballmann M. Derichs N, et al. Among authors: bijman j. Pediatr Res. 2004 Jan;55(1):69-75. doi: 10.1203/01.PDR.0000100758.66805.CE. Epub 2003 Nov 6. Pediatr Res. 2004. PMID: 14605249
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.
De Zeeuw CI, Chorev E, Devor A, Manor Y, Van Der Giessen RS, De Jeu MT, Hoogenraad CC, Bijman J, Ruigrok TJ, French P, Jaarsma D, Kistler WM, Meier C, Petrasch-Parwez E, Dermietzel R, Sohl G, Gueldenagel M, Willecke K, Yarom Y. De Zeeuw CI, et al. Among authors: bijman j. J Neurosci. 2003 Jun 1;23(11):4700-11. doi: 10.1523/JNEUROSCI.23-11-04700.2003. J Neurosci. 2003. PMID: 12805309 Free PMC article.
Who is driving biotechnology acceptance?
Kalaitzandonakes N, Bijman J. Kalaitzandonakes N, et al. Among authors: bijman j. Nat Biotechnol. 2003 Apr;21(4):366-9. doi: 10.1038/nbt0403-366. Nat Biotechnol. 2003. PMID: 12665818 No abstract available.
67 results