H Cuppens - JoVE Visualize

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Genetic Counseling (Geneva, Switzerland)|January 1, 1992

An Algerian child homozygous for the M470V polymorphism and for a deletion of two nucleotides in exon 10 of the CFTR gene, shows severe cystic fibrosis symptomsO Loumi, H Cuppens, R Bakour, et al.

FEBS Letters|November 6, 1998

Characterization of mutations located in exon 18 of the CFTR geneA Vankeerberghen, L Wei, H Teng, et al.

Thorax|December 31, 2005

Cystic fibrosis: terminology and diagnostic algorithmsK De Boeck, M Wilschanski, C Castellani, et al.

Prenatal Diagnosis|December 1, 1993

Co-amplification of the cystic fibrosis delta F508 mutation with the HLA DQA1 sequence in single cell PCR: implications for improved assessment of polar bodies and blastomeres in preimplantation diagnosisR Wu, H Cuppens, I Buyse, et al.

Molecular Reproduction and Development|January 5, 2000

Morphological changes in the vas deferens and expression of the cystic fibrosis transmembrane conductance regulator (CFTR) in control, deltaF508 and knock-out CFTR mice during postnatal lifeI Reynaert, B Van Der Schueren, G Degeest, et al.

BMC Physiology|May 18, 2001

Functional interaction between TRP4 and CFTR in mouse aorta endothelial cellsL Wei, M Freichel, M Jaspers, et al.

Journal of Medical Genetics|July 1, 1995

Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSASJ C Ruiz, H Cuppens, E Legius, et al.

Tissue Antigens|January 1, 1993

Rapid DNA typing of class II HLA antigens using the polymerase chain reaction and reverse dot blot hybridizationI Buyse, R Decorte, M Baens, et al.

FEBS Letters|May 5, 1997

A novel model for the first nucleotide binding domain of the cystic fibrosis transmembrane conductance regulatorJ P Annereau, U Wulbrand, A Vankeerberghen, et al.

The Journal of Physiology|February 2, 1999

Inhibition of volume-regulated anion channels by expression of the cystic fibrosis transmembrane conductance regulatorR Vennekens, D Trouet, A Vankeerberghen, et al.

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Showing results (21-30 of 42) with videos related to

Sort By:

Pageof 5

Genetic Counseling (Geneva, Switzerland)|January 1, 1992

An Algerian child homozygous for the M470V polymorphism and for a deletion of two nucleotides in exon 10 of the CFTR gene, shows severe cystic fibrosis symptomsO Loumi, H Cuppens, R Bakour, et al.

FEBS Letters|November 6, 1998

Characterization of mutations located in exon 18 of the CFTR geneA Vankeerberghen, L Wei, H Teng, et al.

Thorax|December 31, 2005

Cystic fibrosis: terminology and diagnostic algorithmsK De Boeck, M Wilschanski, C Castellani, et al.

Prenatal Diagnosis|December 1, 1993

Co-amplification of the cystic fibrosis delta F508 mutation with the HLA DQA1 sequence in single cell PCR: implications for improved assessment of polar bodies and blastomeres in preimplantation diagnosisR Wu, H Cuppens, I Buyse, et al.

Molecular Reproduction and Development|January 5, 2000

Morphological changes in the vas deferens and expression of the cystic fibrosis transmembrane conductance regulator (CFTR) in control, deltaF508 and knock-out CFTR mice during postnatal lifeI Reynaert, B Van Der Schueren, G Degeest, et al.

BMC Physiology|May 18, 2001

Functional interaction between TRP4 and CFTR in mouse aorta endothelial cellsL Wei, M Freichel, M Jaspers, et al.

Journal of Medical Genetics|July 1, 1995

Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSASJ C Ruiz, H Cuppens, E Legius, et al.

Tissue Antigens|January 1, 1993

Rapid DNA typing of class II HLA antigens using the polymerase chain reaction and reverse dot blot hybridizationI Buyse, R Decorte, M Baens, et al.

FEBS Letters|May 5, 1997

A novel model for the first nucleotide binding domain of the cystic fibrosis transmembrane conductance regulatorJ P Annereau, U Wulbrand, A Vankeerberghen, et al.

The Journal of Physiology|February 2, 1999

Inhibition of volume-regulated anion channels by expression of the cystic fibrosis transmembrane conductance regulatorR Vennekens, D Trouet, A Vankeerberghen, et al.

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