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Susanne Stary

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

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Bone|June 23, 2012
A novel homozygous mutation in the parathyroid hormone gene (PTH) in a girl with isolated hypoparathyroidismDiana-Alexandra Ertl, Susanne Stary, Berthold Streubel, et al.
Prenatal Diagnosis|October 26, 2011
Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defectsMaximilian Schmid, Susanne Stary, Wibke Blaicher, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|August 14, 2012
Interleukin-1 beta gene polymorphisms and preterm birthMaximilian Schmid, Peter Haslinger, Susanne Stary, et al.
Genes, Chromosomes & Cancer|September 12, 2012
t(11;14)(q23;q32) involving IGH and DDX6 in nodal marginal zone lymphomaSusanne Stary, Ursula Vinatzer, Leonhard Müllauer, et al.
Journal of Neuropathology and Experimental Neurology|July 16, 2011
Value and limitations of immunohistochemistry and gene sequencing for detection of the IDH1-R132H mutation in diffuse glioma biopsy specimensMatthias Preusser, Adelheid Wöhrer, Susanne Stary, et al.
Plant Physiology|October 11, 2003
PRT1 of Arabidopsis is a ubiquitin protein ligase of the plant N-end rule pathway with specificity for aromatic amino-terminal residuesSusanne Stary, Xiao-jun Yin, Thomas Potuschak, et al.
The American Journal of Surgical Pathology|January 29, 2008
Autoimmune lymphoproliferative syndrome (ALPS) caused by Fas (CD95) mutation mimicking sarcoidosisLeonhard Müllauer, Josef Emhofer, Sabine Wohlfart, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 22, 2012
MAPKAP kinase 2 overexpression influences prognosis in gastrointestinal stromal tumors and associates with copy number variations on chromosome 1 and expression of p38 MAP kinase and ETV1Peter Birner, Andrea Beer, Ursula Vinatzer, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|June 25, 2014
Global and single gene DNA methylation in umbilical cord blood cells after elective caesarean: a pilot studyMaximilian B Franz, Mariella Poterauer, Marie Elhenicky, et al.
Lancet (London, England)|December 3, 2011
Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in AustriaThomas P Mechtler, Susanne Stary, Thomas F Metz, et al.
Pageof 1

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

Sort By:
Pageof 1
Bone|June 23, 2012
A novel homozygous mutation in the parathyroid hormone gene (PTH) in a girl with isolated hypoparathyroidismDiana-Alexandra Ertl, Susanne Stary, Berthold Streubel, et al.
Prenatal Diagnosis|October 26, 2011
Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defectsMaximilian Schmid, Susanne Stary, Wibke Blaicher, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|August 14, 2012
Interleukin-1 beta gene polymorphisms and preterm birthMaximilian Schmid, Peter Haslinger, Susanne Stary, et al.
Genes, Chromosomes & Cancer|September 12, 2012
t(11;14)(q23;q32) involving IGH and DDX6 in nodal marginal zone lymphomaSusanne Stary, Ursula Vinatzer, Leonhard Müllauer, et al.
Journal of Neuropathology and Experimental Neurology|July 16, 2011
Value and limitations of immunohistochemistry and gene sequencing for detection of the IDH1-R132H mutation in diffuse glioma biopsy specimensMatthias Preusser, Adelheid Wöhrer, Susanne Stary, et al.
Plant Physiology|October 11, 2003
PRT1 of Arabidopsis is a ubiquitin protein ligase of the plant N-end rule pathway with specificity for aromatic amino-terminal residuesSusanne Stary, Xiao-jun Yin, Thomas Potuschak, et al.
The American Journal of Surgical Pathology|January 29, 2008
Autoimmune lymphoproliferative syndrome (ALPS) caused by Fas (CD95) mutation mimicking sarcoidosisLeonhard Müllauer, Josef Emhofer, Sabine Wohlfart, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 22, 2012
MAPKAP kinase 2 overexpression influences prognosis in gastrointestinal stromal tumors and associates with copy number variations on chromosome 1 and expression of p38 MAP kinase and ETV1Peter Birner, Andrea Beer, Ursula Vinatzer, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|June 25, 2014
Global and single gene DNA methylation in umbilical cord blood cells after elective caesarean: a pilot studyMaximilian B Franz, Mariella Poterauer, Marie Elhenicky, et al.
Lancet (London, England)|December 3, 2011
Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in AustriaThomas P Mechtler, Susanne Stary, Thomas F Metz, et al.
Pageof 1