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J Ligtenberg

Showing results (101-110 of 136) with videos related to

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Clinical and Experimental Immunology|May 22, 2001
Suppression of the clinical and cytokine response to endotoxin by RWJ-67657, a p38 mitogen-activated protein-kinase inhibitor, in healthy human volunteersJ W Fijen, J G Zijlstra, P De Boer, et al.
BMC Women'S Health|May 10, 2012
DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-directAisha S Sie, Liesbeth Spruijt, Wendy A G van Zelst-Stams, et al.
Human Genetics|July 1, 1995
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutationA F van Lieburg, M A Verdijk, F Schoute, et al.
Plos One|April 18, 2015
EMAST is associated with a poor prognosis in microsatellite instable metastatic colorectal cancerSabine Venderbosch, Shannon van Lent-van Vliet, Anton F J de Haan, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 15, 1993
Episialin (MUC1) inhibits cytotoxic lymphocyte-target cell interactionE van de Wiel-van Kemenade, M J Ligtenberg, A J de Boer, et al.
Human Reproduction (Oxford, England)|October 2, 1998
Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor geneJ H Tuerlings, M J Ligtenberg, J A Kremer, et al.
British Journal of Haematology|November 18, 2003
Mutual exclusion of t(11;18)(q21;q21) and numerical chromosomal aberrations in the development of different types of primary gastric lymphomasMax I Schreuder, Marieke A Hoeve, Konnie M Hebeda, et al.
American Journal of Human Genetics|May 1, 1995
The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter regionM Wijker, M J Ligtenberg, F Schoute, et al.
American Journal of Human Genetics|January 1, 1995
Spectrum of mutations in the gene encoding the adrenoleukodystrophy proteinM J Ligtenberg, S Kemp, C O Sarde, et al.
Neuromuscular Disorders : NMD|October 20, 2020
Myotonic dystrophy and recurrent pleomorphic adenomas: Case report and association hypothesisIneke M J Pruijn, Carla M L van Herpen, Sjoert A H Pegge, et al.
Pageof 14

Showing results (101-110 of 136) with videos related to

Sort By:
Pageof 14
Clinical and Experimental Immunology|May 22, 2001
Suppression of the clinical and cytokine response to endotoxin by RWJ-67657, a p38 mitogen-activated protein-kinase inhibitor, in healthy human volunteersJ W Fijen, J G Zijlstra, P De Boer, et al.
BMC Women'S Health|May 10, 2012
DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-directAisha S Sie, Liesbeth Spruijt, Wendy A G van Zelst-Stams, et al.
Human Genetics|July 1, 1995
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutationA F van Lieburg, M A Verdijk, F Schoute, et al.
Plos One|April 18, 2015
EMAST is associated with a poor prognosis in microsatellite instable metastatic colorectal cancerSabine Venderbosch, Shannon van Lent-van Vliet, Anton F J de Haan, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 15, 1993
Episialin (MUC1) inhibits cytotoxic lymphocyte-target cell interactionE van de Wiel-van Kemenade, M J Ligtenberg, A J de Boer, et al.
Human Reproduction (Oxford, England)|October 2, 1998
Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor geneJ H Tuerlings, M J Ligtenberg, J A Kremer, et al.
British Journal of Haematology|November 18, 2003
Mutual exclusion of t(11;18)(q21;q21) and numerical chromosomal aberrations in the development of different types of primary gastric lymphomasMax I Schreuder, Marieke A Hoeve, Konnie M Hebeda, et al.
American Journal of Human Genetics|May 1, 1995
The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter regionM Wijker, M J Ligtenberg, F Schoute, et al.
American Journal of Human Genetics|January 1, 1995
Spectrum of mutations in the gene encoding the adrenoleukodystrophy proteinM J Ligtenberg, S Kemp, C O Sarde, et al.
Neuromuscular Disorders : NMD|October 20, 2020
Myotonic dystrophy and recurrent pleomorphic adenomas: Case report and association hypothesisIneke M J Pruijn, Carla M L van Herpen, Sjoert A H Pegge, et al.
Pageof 14