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Results 1 - 10 of 17  for Great Falls College MSU

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Phosphorylation site independent single R-domain mutations affect CFTR channel activity.

Wei, L ; Vankeerberghen, A ; Cuppens, H ; Droogmans, G ; Cassiman, J J ; Nilius, B Wei, L (correspondence author) ; Wei, L (record owner)

FEBS letters, November 13, 1998, Vol.439(1-2), pp.121-126 [Peer Reviewed Journal]

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Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities

Frauke Becker ; Carla G Van El ; Dolores Ibarreta ; Eleni Zika ; Stuart Hogarth ; Pascal Borry ; Anne Cambon-Thomsen ; Jean Jacques Cassiman ; Gerry Evers-Kiebooms ; Shirley Hodgson ; A Cécile J W Janssens ; Helena Kaariainen ; Michael Krawczak ; Ulf Kristoffersson ; Jan Lubinski ; Christine Patch ; Victor B Penchaszadeh ; Andrew Read ; Wolf Rogowski ; Jorge Sequeiros ; Lisbeth Tranebjaerg ; Irene M Van Langen ; Helen Wallace ; Ron Zimmern ; Jörg Schmidtke ; Martina C Cornel

European Journal of Human Genetics, 2011, Vol.19(S1), p.S6 [Peer Reviewed Journal]

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Functional Characterization of the CFTR R Domain Using CFTR/MDR1 Hybrid and Deletion Constructs

Vankeerberghen, A ; Lin, Wei ; Jaspers, M ; Cuppens, H ; Nilius, B ; Cassiman, J-J Vankeerberghen, A (correspondence author)

Biochemistry (Washington), Nov 1999, Vol.38(45), pp.14988-14998 [Peer Reviewed Journal]

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A novel model for the first nucleotide binding domain of the cystic fibrosis transmembrane conductance regulator.

Annereau, J P ; Wulbrand, U ; Vankeerberghen, A ; Cuppens, H ; Bontems, F ; Tümmler, B ; Cassiman, J J ; Stoven, V Annereau, J P (correspondence author) ; Annereau, J P (record owner)

FEBS letters, May 5, 1997, Vol.407(3), pp.303-308 [Peer Reviewed Journal]

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Characterization of mutations located in exon 18 of the CFTR gene.

Vankeerberghen, A ; Wei, L ; Teng, H ; Jaspers, M ; Cassiman, J J ; Nilius, B ; Cuppens, H Vankeerberghen, A (correspondence author) ; Vankeerberghen, A (record owner)

FEBS letters, October 16, 1998, Vol.437(1-2), pp.1-4 [Peer Reviewed Journal]

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Benchmarks for cystic fibrosis carrier screening: a European consensus document

Castellani, C. ; Macek, M. ; Cassiman, J.J. ; Duff, A. ; Massie, J. ; ten Kate, L.P. ; Barton, D ; Cutting, G. ; Dallapiccola, B. ; Dequeker, E. ; Girodon, E. ; Grody, W. ; Highsmith, E.W. ; Kaariainen, H. ; Kruip, S. ; Morris, M. ; Pignatti, P.F. ; Pypops, U. ; Schwarz, M. ; Soller, M. Clinical genetics ; EMGO - Quality of care

Journal of Cystic Fibrosis, 2010, Vol.9(3), pp.165-178 [Peer Reviewed Journal]

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Developmental changes in heparan sulfate expression: in situ detection with mAbs.

David, G ; Bai, X M ; Van Der Schueren, B ; Cassiman, J J ; Van Den Berghe, H David, G (correspondence author) ; David, G (record owner)

The Journal of cell biology, November 1992, Vol.119(4), pp.961-975 [Peer Reviewed Journal]

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Molecular cloning of amphiglycan, a novel integral membrane heparan sulfate proteoglycan expressed by epithelial and fibroblastic cells

David, G ; Van Der Schueren, B ; Marynen, P ; Cassiman, J J ; Van Den Berghe, H

The Journal of cell biology, August 1992, Vol.118(4), pp.961-9 [Peer Reviewed Journal]

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Differential splicing of COL4A5 mRNA in kidney and white blood cells: a complex mutation in the COL4A5 gene of an Alport patient deletes the NC1 domain.

Guo, C ; Van Damme, B ; Van Damme-Lombaerts, R ; Van Den Berghe, H ; Cassiman, J J ; Marynen, P Guo, C (correspondence author) ; Guo, C (record owner)

Kidney international, December 1993, Vol.44(6), pp.1316-1321 [Peer Reviewed Journal]

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Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor).

Tejpar, S ; Nollet, F ; Li, C ; Wunder, J S ; Michils, G ; Dal Cin, P ; Van Cutsem, E ; Bapat, B ; van Roy, F ; Cassiman, J J ; Alman, B A Tejpar, S (correspondence author) ; Tejpar, S (record owner)

Oncogene, November 11, 1999, Vol.18(47), pp.6615-6620 [Peer Reviewed Journal]

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