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Showing results (301-310 of 391) with videos related to

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 24, 2012
Copeptin, a surrogate marker for vasopressin, is associated with kidney function decline in subjects with autosomal dominant polycystic kidney diseaseWendy E Boertien, Esther Meijer, Debbie Zittema, et al.
Nature Genetics|June 30, 2001
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosisO T Njajou, N Vaessen, M Joosse, et al.
American Journal of Medical Genetics. Part A|November 6, 2004
Three new families with arterial tortuosity syndromeMarja W Wessels, Coriene E Catsman-Berrevoets, Grazia M S Mancini, et al.
European Journal of Medical Genetics|June 14, 2011
Three new cases with a mosaicism involving a normal cell line and a cryptic unbalanced autosomal reciprocal translocationAntoinet C J Gijsbers, Johannes G Dauwerse, Cathy A J Bosch, et al.
The Journal of Biological Chemistry|April 17, 2004
Aberrant polycystin-1 expression results in modification of activator protein-1 activity, whereas Wnt signaling remains unaffectedNgoc Hang Le, Paola van der Bent, Gerwin Huls, et al.
Stroke|February 3, 2007
Lacunar infarcts are the main correlate with cognitive dysfunction in CADASILMichael K Liem, Jeroen van der Grond, Joost Haan, et al.
Journal of Medicinal Chemistry|February 6, 2010
Michael acceptor based antiplasmodial and antitrypanosomal cysteine protease inhibitors with unusual amino acidsAlexander Breuning, Björn Degel, Franziska Schulz, et al.
Journal of Clinical Immunology|March 3, 2016
Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patientsInge C de Vor, Pomme M van der Meulen, Vincent Bekker, et al.
British Journal of Haematology|July 26, 2002
Minimal residual disease quantification in patients with acute myeloid leukaemia and inv(16)/CBFB-MYH11 gene fusionBert A van der Reijden, Annet Simons, Erna Luiten, et al.
European Journal of Medical Genetics|June 15, 2010
Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypesAntoinet C J Gijsbers, Cathy A J Bosch, Johannes G Dauwerse, et al.
Pageof 40

Showing results (301-310 of 391) with videos related to

Sort By:
Pageof 40
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 24, 2012
Copeptin, a surrogate marker for vasopressin, is associated with kidney function decline in subjects with autosomal dominant polycystic kidney diseaseWendy E Boertien, Esther Meijer, Debbie Zittema, et al.
Nature Genetics|June 30, 2001
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosisO T Njajou, N Vaessen, M Joosse, et al.
American Journal of Medical Genetics. Part A|November 6, 2004
Three new families with arterial tortuosity syndromeMarja W Wessels, Coriene E Catsman-Berrevoets, Grazia M S Mancini, et al.
European Journal of Medical Genetics|June 14, 2011
Three new cases with a mosaicism involving a normal cell line and a cryptic unbalanced autosomal reciprocal translocationAntoinet C J Gijsbers, Johannes G Dauwerse, Cathy A J Bosch, et al.
The Journal of Biological Chemistry|April 17, 2004
Aberrant polycystin-1 expression results in modification of activator protein-1 activity, whereas Wnt signaling remains unaffectedNgoc Hang Le, Paola van der Bent, Gerwin Huls, et al.
Stroke|February 3, 2007
Lacunar infarcts are the main correlate with cognitive dysfunction in CADASILMichael K Liem, Jeroen van der Grond, Joost Haan, et al.
Journal of Medicinal Chemistry|February 6, 2010
Michael acceptor based antiplasmodial and antitrypanosomal cysteine protease inhibitors with unusual amino acidsAlexander Breuning, Björn Degel, Franziska Schulz, et al.
Journal of Clinical Immunology|March 3, 2016
Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patientsInge C de Vor, Pomme M van der Meulen, Vincent Bekker, et al.
British Journal of Haematology|July 26, 2002
Minimal residual disease quantification in patients with acute myeloid leukaemia and inv(16)/CBFB-MYH11 gene fusionBert A van der Reijden, Annet Simons, Erna Luiten, et al.
European Journal of Medical Genetics|June 15, 2010
Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypesAntoinet C J Gijsbers, Cathy A J Bosch, Johannes G Dauwerse, et al.
Pageof 40