J de Kok - JoVE Visualize

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Journal of Plant Physiology|December 22, 2009

Copper exposure interferes with the regulation of the uptake, distribution and metabolism of sulfate in Chinese cabbageMuhammad Shahbaz, Mei Hwei Tseng, C Elisabeth E Stuiver, et al.

Science (New York, N.Y.)|February 3, 1995

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.

Genomics|June 22, 1999

Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridizationA I den Hollander, M A van Driel, Y J de Kok, et al.

Human Molecular Genetics|July 1, 1994

X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.

European Journal of Human Genetics : EJHG|January 1, 1995

Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardationS M van der Maarel, I H Scholten, J A Maat-Kievit, et al.

Human Molecular Genetics|February 5, 1999

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defectsY J de Kok, S J Bom, T M Brunt, et al.

Annals of Surgery|October 1, 2019

The Neglectable Impact of Delayed Graft Function on Long-term Graft Survival in Kidneys Donated After Circulatory Death Associates With Superior Organ ResilienceMichèle J de Kok, Dagmara McGuinness, Paul G Shiels, et al.

Kidney International|May 4, 2020

A nationwide evaluation of deceased donor kidney transplantation indicates detrimental consequences of early graft lossMichèle J de Kok, Alexander F Schaapherder, Jacobus W Mensink, et al.

Human Molecular Genetics|September 1, 1996

Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4Y J de Kok, E R Vossenaar, C W Cremers, et al.

American Journal of Human Genetics|June 5, 2001

Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) geneA I den Hollander, J R Heckenlively, L I van den Born, et al.

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Showing results (101-110 of 112) with videos related to

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Journal of Plant Physiology|December 22, 2009

Copper exposure interferes with the regulation of the uptake, distribution and metabolism of sulfate in Chinese cabbageMuhammad Shahbaz, Mei Hwei Tseng, C Elisabeth E Stuiver, et al.

Science (New York, N.Y.)|February 3, 1995

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.

Genomics|June 22, 1999

Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridizationA I den Hollander, M A van Driel, Y J de Kok, et al.

Human Molecular Genetics|July 1, 1994

X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.

European Journal of Human Genetics : EJHG|January 1, 1995

Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardationS M van der Maarel, I H Scholten, J A Maat-Kievit, et al.

Human Molecular Genetics|February 5, 1999

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defectsY J de Kok, S J Bom, T M Brunt, et al.

Annals of Surgery|October 1, 2019

The Neglectable Impact of Delayed Graft Function on Long-term Graft Survival in Kidneys Donated After Circulatory Death Associates With Superior Organ ResilienceMichèle J de Kok, Dagmara McGuinness, Paul G Shiels, et al.

Kidney International|May 4, 2020

A nationwide evaluation of deceased donor kidney transplantation indicates detrimental consequences of early graft lossMichèle J de Kok, Alexander F Schaapherder, Jacobus W Mensink, et al.

Human Molecular Genetics|September 1, 1996

Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4Y J de Kok, E R Vossenaar, C W Cremers, et al.

American Journal of Human Genetics|June 5, 2001

Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) geneA I den Hollander, J R Heckenlively, L I van den Born, et al.

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