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G Brunner

Showing results (261-270 of 727) with videos related to

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Familial Cancer|December 8, 2009
Female BRCA mutation carriers with a preference for prophylactic mastectomy are more likely to participate an educational-support group and to proceed with the preferred intervention within 2 yearsKarin M Landsbergen, Judith B Prins, Yvonne J L Kamm, et al.
European Journal of Immunology|September 1, 1991
Coordinate secretion and functional synergism of T cell-associated serine proteinase-1 (MTSP-1) and endoglycosidase(s) of activated T cellsU Vettel, R Bar-Shavit, M M Simon, et al.
Biomaterials, Medical Devices, and Artificial Organs|January 1, 1978
Large agarose beads for extracorporeal detoxification systemsH Lösgen, G Brunner, C J Holloway, et al.
Biological Psychiatry|July 20, 2010
Genetic variation in CACNA1C, a gene associated with bipolar disorder, influences brainstem rather than gray matter volume in healthy individualsBarbara Franke, Alejandro Arias Vasquez, Joris A Veltman, et al.
American Journal of Medical Genetics|April 24, 1999
Craniosynostosis associated with ectopia lentis in monozygotic twin sistersJ R Cruysberg, C M van Ravenswaaij-Arts, A Pinckers, et al.
European Journal of Human Genetics : EJHG|February 24, 2006
A text-mining analysis of the human phenomeMarc A van Driel, Jorn Bruggeman, Gert Vriend, et al.
Annales De Genetique|May 4, 2001
The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR)G J Van Buggenhout, J C Trommelen, H G Brunner, et al.
European Journal of Clinical Investigation|August 1, 1995
Four week administration of an ACE inhibitor and a cardioselective beta-blocker in healthy volunteers: no influence on insulin sensitivityL Heinemann, T Heise, J Ampudia, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Molecular genetics of X-linked hearing impairmentH G Brunner, B Smeets, D Smeets, et al.
The Journal of Clinical Endocrinology and Metabolism|June 18, 1999
Analysis of mutations in genes of the follicle-stimulating hormone receptor signaling pathway in ovarian granulosa cell tumorsM J Ligtenberg, M Siers, A P Themmen, et al.
Pageof 73

Showing results (261-270 of 727) with videos related to

Sort By:
Pageof 73
Familial Cancer|December 8, 2009
Female BRCA mutation carriers with a preference for prophylactic mastectomy are more likely to participate an educational-support group and to proceed with the preferred intervention within 2 yearsKarin M Landsbergen, Judith B Prins, Yvonne J L Kamm, et al.
European Journal of Immunology|September 1, 1991
Coordinate secretion and functional synergism of T cell-associated serine proteinase-1 (MTSP-1) and endoglycosidase(s) of activated T cellsU Vettel, R Bar-Shavit, M M Simon, et al.
Biomaterials, Medical Devices, and Artificial Organs|January 1, 1978
Large agarose beads for extracorporeal detoxification systemsH Lösgen, G Brunner, C J Holloway, et al.
Biological Psychiatry|July 20, 2010
Genetic variation in CACNA1C, a gene associated with bipolar disorder, influences brainstem rather than gray matter volume in healthy individualsBarbara Franke, Alejandro Arias Vasquez, Joris A Veltman, et al.
American Journal of Medical Genetics|April 24, 1999
Craniosynostosis associated with ectopia lentis in monozygotic twin sistersJ R Cruysberg, C M van Ravenswaaij-Arts, A Pinckers, et al.
European Journal of Human Genetics : EJHG|February 24, 2006
A text-mining analysis of the human phenomeMarc A van Driel, Jorn Bruggeman, Gert Vriend, et al.
Annales De Genetique|May 4, 2001
The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR)G J Van Buggenhout, J C Trommelen, H G Brunner, et al.
European Journal of Clinical Investigation|August 1, 1995
Four week administration of an ACE inhibitor and a cardioselective beta-blocker in healthy volunteers: no influence on insulin sensitivityL Heinemann, T Heise, J Ampudia, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Molecular genetics of X-linked hearing impairmentH G Brunner, B Smeets, D Smeets, et al.
The Journal of Clinical Endocrinology and Metabolism|June 18, 1999
Analysis of mutations in genes of the follicle-stimulating hormone receptor signaling pathway in ovarian granulosa cell tumorsM J Ligtenberg, M Siers, A P Themmen, et al.
Pageof 73