N V A M Knoers - JoVE Visualize

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Nederlands Tijdschrift Voor Geneeskunde|February 27, 2003

[From gene to disease; the nail-patella syndrome and the LMX1B gene]E M H F Bongers, N V A M Knoers

Molecular Biology of the Cell|October 8, 2004

Regulation of the vasopressin V2 receptor by vasopressin in polarized renal collecting duct cellsJ H Robben, N V A M Knoers, P M T Deen

American Journal of Physiology. Renal Physiology|July 12, 2005

Characterization of vasopressin V2 receptor mutants in nephrogenic diabetes insipidus in a polarized cell modelJ H Robben, N V A M Knoers, P M T Deen

Cytogenetic and Genome Research|November 17, 2011

From karyotyping to array-CGH in prenatal diagnosisK D Lichtenbelt, N V A M Knoers, G H Schuring-Blom

American Journal of Physiology. Renal Physiology|August 24, 2006

Functional rescue of vasopressin V2 receptor mutants in MDCK cells by pharmacochaperones: relevance to therapy of nephrogenic diabetes insipidusJ H Robben, M Sze, N V A M Knoers, et al.

Molecular Biology of the Cell|November 4, 2005

Rescue of vasopressin V2 receptor mutants by chemical chaperones: specificity and mechanismJ H Robben, M Sze, N V A M Knoers, et al.

Nederlands Tijdschrift Voor Geneeskunde|September 25, 2002

[Friedrich's ataxia: clinical difficulties and genetic possibilities]B P C van de Warrenburg, N V A M Knoers, H P H Kremer

Clinical Genetics|September 7, 2005

Human syndromes with congenital patellar anomalies and the underlying gene defectsE M H F Bongers, A van Kampen, H van Bokhoven, et al.

Nederlands Tijdschrift Voor Geneeskunde|July 13, 2005

[From gene to disease; mutations in the SLC12A3 gene as the cause of Gitelman's syndrome]E A M Cornelissen, R J M Bindels, L H Hoefsloot, et al.

Nederlands Tijdschrift Voor Geneeskunde|April 24, 2007

[From gene to disease; 'apparent mineralocorticoid excess' syndrome, a syndrome with an apparent excess of mineral corticoids]E N Levtchenko, J Deinum, N V A M Knoers, et al.

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Showing results (1-10 of 17) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|February 27, 2003

[From gene to disease; the nail-patella syndrome and the LMX1B gene]E M H F Bongers, N V A M Knoers

Molecular Biology of the Cell|October 8, 2004

Regulation of the vasopressin V2 receptor by vasopressin in polarized renal collecting duct cellsJ H Robben, N V A M Knoers, P M T Deen

American Journal of Physiology. Renal Physiology|July 12, 2005

Characterization of vasopressin V2 receptor mutants in nephrogenic diabetes insipidus in a polarized cell modelJ H Robben, N V A M Knoers, P M T Deen

Cytogenetic and Genome Research|November 17, 2011

From karyotyping to array-CGH in prenatal diagnosisK D Lichtenbelt, N V A M Knoers, G H Schuring-Blom

American Journal of Physiology. Renal Physiology|August 24, 2006

Functional rescue of vasopressin V2 receptor mutants in MDCK cells by pharmacochaperones: relevance to therapy of nephrogenic diabetes insipidusJ H Robben, M Sze, N V A M Knoers, et al.

Molecular Biology of the Cell|November 4, 2005

Rescue of vasopressin V2 receptor mutants by chemical chaperones: specificity and mechanismJ H Robben, M Sze, N V A M Knoers, et al.

Nederlands Tijdschrift Voor Geneeskunde|September 25, 2002

[Friedrich's ataxia: clinical difficulties and genetic possibilities]B P C van de Warrenburg, N V A M Knoers, H P H Kremer

Clinical Genetics|September 7, 2005

Human syndromes with congenital patellar anomalies and the underlying gene defectsE M H F Bongers, A van Kampen, H van Bokhoven, et al.

Nederlands Tijdschrift Voor Geneeskunde|July 13, 2005

[From gene to disease; mutations in the SLC12A3 gene as the cause of Gitelman's syndrome]E A M Cornelissen, R J M Bindels, L H Hoefsloot, et al.

Nederlands Tijdschrift Voor Geneeskunde|April 24, 2007

[From gene to disease; 'apparent mineralocorticoid excess' syndrome, a syndrome with an apparent excess of mineral corticoids]E N Levtchenko, J Deinum, N V A M Knoers, et al.

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