T Callens - JoVE Visualize

Showing results (1-10 of 10) with videos related to

Pageof 1

Sort By:

Haemostasis|August 5, 1998

Identification of two different mutations causing protein S deficiency in two unrelated Belgian families using a nonisotopic scanning and sequencing methodL Messiaen, T Callens, G Baele

Human Genetics|January 7, 1998

Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 geneL Messiaen, T Callens, A De Paepe, et al.

Biochemical and Biophysical Research Communications|November 25, 1998

Human myosin V gene produces different transcripts in a cell type-specific mannerJ Lambert, J M Naeyaert, T Callens, et al.

Heredity|May 17, 2012

Genetic diversity and population structure in contemporary house sparrow populations along an urbanization gradientC Vangestel, J Mergeay, D A Dawson, et al.

Molecular Ecology|February 14, 2015

Post-fragmentation population structure in a cooperative breeding Afrotropical cloud forest bird: emergence of a source-sink population networkM Husemann, L Cousseau, T Callens, et al.

Human Mutation|June 22, 2000

Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defectsL M Messiaen, T Callens, G Mortier, et al.

Human Mutation|February 22, 2007

Extensive in silico analysis of NF1 splicing defects uncovers determinants for splicing outcome upon 5' splice-site disruptionK Wimmer, X Roca, H Beiglböck, et al.

Genes, Chromosomes & Cancer|November 12, 2005

Spectrum of single- and multiexon NF1 copy number changes in a cohort of 1,100 unselected NF1 patientsK Wimmer, S Yao, K Claes, et al.

Ecology|September 26, 2015

A stochastic movement simulator improves estimates of landscape connectivityA Coulon, J Aben, S C F Palmer, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001

Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicingL M Messiaen, T Callens, K J Roux, et al.

Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:

Pageof 1

Haemostasis|August 5, 1998

Identification of two different mutations causing protein S deficiency in two unrelated Belgian families using a nonisotopic scanning and sequencing methodL Messiaen, T Callens, G Baele

Human Genetics|January 7, 1998

Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 geneL Messiaen, T Callens, A De Paepe, et al.

Biochemical and Biophysical Research Communications|November 25, 1998

Human myosin V gene produces different transcripts in a cell type-specific mannerJ Lambert, J M Naeyaert, T Callens, et al.

Heredity|May 17, 2012

Genetic diversity and population structure in contemporary house sparrow populations along an urbanization gradientC Vangestel, J Mergeay, D A Dawson, et al.

Molecular Ecology|February 14, 2015

Post-fragmentation population structure in a cooperative breeding Afrotropical cloud forest bird: emergence of a source-sink population networkM Husemann, L Cousseau, T Callens, et al.

Human Mutation|June 22, 2000

Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defectsL M Messiaen, T Callens, G Mortier, et al.

Human Mutation|February 22, 2007

Extensive in silico analysis of NF1 splicing defects uncovers determinants for splicing outcome upon 5' splice-site disruptionK Wimmer, X Roca, H Beiglböck, et al.

Genes, Chromosomes & Cancer|November 12, 2005

Spectrum of single- and multiexon NF1 copy number changes in a cohort of 1,100 unselected NF1 patientsK Wimmer, S Yao, K Claes, et al.

Ecology|September 26, 2015

A stochastic movement simulator improves estimates of landscape connectivityA Coulon, J Aben, S C F Palmer, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001

Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicingL M Messiaen, T Callens, K J Roux, et al.

Pageof 1