Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Heike Dietrich"'
Autor:
Junxian Zhou, Kang Liu, Chris Bauer, Gerald Bendner, Heike Dietrich, Jakub Peter Slivka, Michael Wink, Michelle B. F. Wong, Mike K. S. Chan, Thomas Skutella
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 7; Pages: 6748
Protein probes, including ultrafiltrates from the placenta (UPla) and lung (ULu) of postnatal rabbits, were investigated in premature senescent HEK293 and HepG2 cells to explore whether they could modulate cellular senescence. Tris-Tricine–PAGE, ge
Autor:
Ulrike-Marie Krause, Birgit Spinath, Eric Klopp, Heike Dietrich, Robin Stark, Frank M. Spinath, Ying Zhang, Roland Brünken
Publikováno v:
European Journal of Psychological Assessment. 36:212-215
Abstract. A growing body of studies has emphasized the need to consider method effects due to positively and negatively worded items for a better understanding of the factorial structure of psychological constructs. In particular, several researchers
Autor:
Ulrike-Marie Krause, Roland Brünken, Frank M. Spinath, Eric Klopp, Birgit Spinath, Heike Dietrich, Robin Stark, Ying Zhang
Publikováno v:
Psychology Learning & Teaching. 14:115-130
The aim of the present study was to introduce a general theoretical model of scientific competencies in higher education and to adapt it to three social sciences, namely psychology, sociology, and political science, by providing evidence from expert
Autor:
Toni Brennan, Aleš Neusar, Jacqui Akhurst, Gareth Davies, Heike Dietrich, Martin Tolley, Dana S. Dunn, Yves Laberge, Ana Cristina Almeida, Ailie Robertson, James D. Demetre
Publikováno v:
Psychology Learning & Teaching. 12:297-319
Autor:
Heike Dietrich, Herwart F. Otto, Juergen Kopitz, Consolato Sergi, Nadja Decker, Johannes Uhl, Peter Rieger, Roland Penzel, Marika Kiessling, Saida Zoubaa, Michael Cantz
Publikováno v:
Human Genetics. 109:421-428
We report a Turkish family with parental consanguinity and at risk for sialidosis type II, an inherited autosomal recessive disorder caused by lysosomal alpha-N-acetyl-neuraminidase (sialidase, NEU1) deficiency. The proband was a premature male infan