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G Matthijs

Showing results (1-10 of 157) with videos related to

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Trends in Biochemical Sciences|September 6, 2000
Congenital disorders of glycosylationG Matthijs
Nucleic Acids Research|September 25, 1991
A deletion polymorphism in the human alpha-2-macroglobulin (A2M) geneG Matthijs, P Marynen
Annual Review of Genomics and Human Genetics|November 10, 2001
Congenital disorders of glycosylationJ Jaeken, G Matthijs
Annals of the New York Academy of Sciences|September 10, 1994
The promoter of the human alpha 2-macroglobulin gene binds HNF-4 or a related nuclear factor for its expression in hepatocytes and lung fibroblastsG Matthijs, P Marynen
Neuropediatrics|June 1, 2000
Congenital disorders of glycosylation (CDG): a rapidly expanding group of neurometabolic disordersS Grünewald, G Matthijs
European Journal of Human Genetics : EJHG|March 21, 2008
Patenting and licensing in genetic testingS Aymé, G Matthijs, S Soini, et al.
The Journal of Physiology|June 1, 1989
Desensitization to cytoplasmic Ca2+ and Ca2+ sensitivities of guinea-pig ileum and rabbit pulmonary artery smooth muscleB Himpens, G Matthijs, A P Somlyo
Prenatal Diagnosis|July 17, 1998
The prenatal diagnosis of spinal muscular atrophyG Matthijs, K Devriendt, J P Fryns
Naunyn-Schmiedeberg'S Archives of Pharmacology|February 1, 1991
Ca2+ dependence of motilide-induced contractions in rabbit duodenal muscle strips in vitroT L Peeters, G Matthijs, G Vantrappen
Genetic Counseling (Geneva, Switzerland)|July 23, 2003
PTPN11 mutation in a young man with Noonan syndrome and retinitis pigmentosaE Schollen, G Matthijs, J F Fryns
Pageof 16

Showing results (1-10 of 157) with videos related to

Sort By:
Pageof 16
Trends in Biochemical Sciences|September 6, 2000
Congenital disorders of glycosylationG Matthijs
Nucleic Acids Research|September 25, 1991
A deletion polymorphism in the human alpha-2-macroglobulin (A2M) geneG Matthijs, P Marynen
Annual Review of Genomics and Human Genetics|November 10, 2001
Congenital disorders of glycosylationJ Jaeken, G Matthijs
Annals of the New York Academy of Sciences|September 10, 1994
The promoter of the human alpha 2-macroglobulin gene binds HNF-4 or a related nuclear factor for its expression in hepatocytes and lung fibroblastsG Matthijs, P Marynen
Neuropediatrics|June 1, 2000
Congenital disorders of glycosylation (CDG): a rapidly expanding group of neurometabolic disordersS Grünewald, G Matthijs
European Journal of Human Genetics : EJHG|March 21, 2008
Patenting and licensing in genetic testingS Aymé, G Matthijs, S Soini, et al.
The Journal of Physiology|June 1, 1989
Desensitization to cytoplasmic Ca2+ and Ca2+ sensitivities of guinea-pig ileum and rabbit pulmonary artery smooth muscleB Himpens, G Matthijs, A P Somlyo
Prenatal Diagnosis|July 17, 1998
The prenatal diagnosis of spinal muscular atrophyG Matthijs, K Devriendt, J P Fryns
Naunyn-Schmiedeberg'S Archives of Pharmacology|February 1, 1991
Ca2+ dependence of motilide-induced contractions in rabbit duodenal muscle strips in vitroT L Peeters, G Matthijs, G Vantrappen
Genetic Counseling (Geneva, Switzerland)|July 23, 2003
PTPN11 mutation in a young man with Noonan syndrome and retinitis pigmentosaE Schollen, G Matthijs, J F Fryns
Pageof 16