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A de Klein

Showing results (31-40 of 83) with videos related to

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American Journal of Ophthalmology|May 20, 1999
Orbital chondrosarcoma developing in a patient with Paget diseaseC M Mooy, N C Naus, A de Klein, et al.
Genomics|November 26, 1998
A human and mouse homolog of the Schizosaccharomyces pombe rad1+ cell cycle checkpoint control geneH A Bluyssen, R I van Os, N C Naus, et al.
Genomics|February 6, 1999
Human and mouse homologs of the Schizosaccharomyces pombe rad17+ cell cycle checkpoint control geneH A Bluyssen, N C Naus, R I van Os, et al.
Experimental Hematology|July 1, 1993
Absence of both subunits of cytochrome b558 in the UM384 cell line relative to the inability to generate superoxide anionsP Champelovier, F Laporte, A J Verhoeven, et al.
Nature|November 17, 1983
Localization of the c-ab1 oncogene adjacent to a translocation break point in chronic myelocytic leukaemiaN Heisterkamp, J R Stephenson, J Groffen, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|November 2, 2012
Etiological and pathogenic factors in congenital diaphragmatic herniaI Sluiter, D Veenma, R van Loenhout, et al.
The New England Journal of Medicine|December 5, 1985
Evidence of a new chimeric bcr/c-abl mRNA in patients with chronic myelocytic leukemia and the Philadelphia chromosomeK Stam, N Heisterkamp, G Grosveld, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 20, 2009
Genetic and environmental factors in the etiology of esophageal atresia and/or tracheoesophageal fistula: an overview of the current conceptsJanine F Felix, Elisabeth M de Jong, Claudine P Torfs, et al.
The Journal of Experimental Medicine|July 1, 1983
c-sis is translocated from chromosome 22 to chromosome 9 in chronic myelocytic leukemiaJ Groffen, N Heisterkamp, J R Stephenson, et al.
American Journal of Human Genetics|November 1, 1992
Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)M de Boer, A de Klein, J P Hossle, et al.
Pageof 9

Showing results (31-40 of 83) with videos related to

Sort By:
Pageof 9
American Journal of Ophthalmology|May 20, 1999
Orbital chondrosarcoma developing in a patient with Paget diseaseC M Mooy, N C Naus, A de Klein, et al.
Genomics|November 26, 1998
A human and mouse homolog of the Schizosaccharomyces pombe rad1+ cell cycle checkpoint control geneH A Bluyssen, R I van Os, N C Naus, et al.
Genomics|February 6, 1999
Human and mouse homologs of the Schizosaccharomyces pombe rad17+ cell cycle checkpoint control geneH A Bluyssen, N C Naus, R I van Os, et al.
Experimental Hematology|July 1, 1993
Absence of both subunits of cytochrome b558 in the UM384 cell line relative to the inability to generate superoxide anionsP Champelovier, F Laporte, A J Verhoeven, et al.
Nature|November 17, 1983
Localization of the c-ab1 oncogene adjacent to a translocation break point in chronic myelocytic leukaemiaN Heisterkamp, J R Stephenson, J Groffen, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|November 2, 2012
Etiological and pathogenic factors in congenital diaphragmatic herniaI Sluiter, D Veenma, R van Loenhout, et al.
The New England Journal of Medicine|December 5, 1985
Evidence of a new chimeric bcr/c-abl mRNA in patients with chronic myelocytic leukemia and the Philadelphia chromosomeK Stam, N Heisterkamp, G Grosveld, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 20, 2009
Genetic and environmental factors in the etiology of esophageal atresia and/or tracheoesophageal fistula: an overview of the current conceptsJanine F Felix, Elisabeth M de Jong, Claudine P Torfs, et al.
The Journal of Experimental Medicine|July 1, 1983
c-sis is translocated from chromosome 22 to chromosome 9 in chronic myelocytic leukemiaJ Groffen, N Heisterkamp, J R Stephenson, et al.
American Journal of Human Genetics|November 1, 1992
Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)M de Boer, A de Klein, J P Hossle, et al.
Pageof 9