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1121.
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1122.
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1123.
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1124.
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1125.
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1126.
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1127.
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1128.
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Kinesin-1 Is a New Actor Involved in Platelet Secretion and Thrombus Stability. [electronic resource] by
- Adam, Frédéric
- Kauskot, Alexandre
- Kurowska, Mathieu
- Goudin, Nicolas
- Munoz, Isabelle
- Bordet, Jean-Claude
- Huang, Jian-Dong
- Bryckaert, Marijke
- Fischer, Alain
- Borgel, Delphine
- de Saint Basile, Geneviève
- Christophe, Olivier D
- Ménasché, Gaël
Producer: 20190708
In:
Arteriosclerosis, thrombosis, and vascular biology vol. 38
Availability: No items available.
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1129.
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1130.
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1131.
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SYNERGISTIC ON AUXIN AND CYTOKININ 1 positively regulates growth and attenuates soil pathogen resistance. [electronic resource] by
- Hurný, Andrej
- Cuesta, Candela
- Cavallari, Nicola
- Ötvös, Krisztina
- Duclercq, Jerome
- Dokládal, Ladislav
- Montesinos, Juan Carlos
- Gallemí, Marçal
- Semerádová, Hana
- Rauter, Thomas
- Stenzel, Irene
- Persiau, Geert
- Benade, Freia
- Bhalearo, Rishikesh
- Sýkorová, Eva
- Gorzsás, András
- Sechet, Julien
- Mouille, Gregory
- Heilmann, Ingo
- De Jaeger, Geert
- Ludwig-Müller, Jutta
- Benková, Eva
Producer: 20200810
In:
Nature communications vol. 11
Availability: No items available.
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1132.
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Mutant prion protein expression is associated with an alteration of the Rab GDP dissociation inhibitor alpha (GDI)/Rab11 pathway. [electronic resource] by
- Massignan, Tania
- Biasini, Emiliano
- Lauranzano, Eliana
- Veglianese, Pietro
- Pignataro, Mauro
- Fioriti, Luana
- Harris, David A
- Salmona, Mario
- Chiesa, Roberto
- Bonetto, Valentina
Producer: 20100817
In:
Molecular & cellular proteomics : MCP vol. 9
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1133.
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1134.
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1135.
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Genetics of cortisol secretion and depressive symptoms: a candidate gene and genome wide association approach. [electronic resource] by
- Velders, Fleur P
- Kuningas, Maris
- Kumari, Meena
- Dekker, Marieke J
- Uitterlinden, Andre G
- Kirschbaum, Clemens
- Hek, Karin
- Hofman, Albert
- Verhulst, Frank C
- Kivimaki, Mika
- Van Duijn, Cornelia M
- Walker, Brian R
- Tiemeier, Henning
Producer: 20111209
In:
Psychoneuroendocrinology vol. 36
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1136.
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1137.
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1138.
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Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion. [electronic resource] by
- Langer, Florian
- Obser, Tobias
- Oyen, Florian
- Spath, Brigitte
- Holstein, Katharina
- Greinacher, Andreas
- White, James G
- Budde, Ulrich
- Bokemeyer, Carsten
- Schneppenheim, Reinhard
Producer: 20150416
In:
Thrombosis and haemostasis vol. 111
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1139.
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1140.
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Mutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic Integrity. [electronic resource] by
- Praschberger, Roman
- Lowe, Simon A
- Malintan, Nancy T
- Giachello, Carlo N G
- Patel, Nian
- Houlden, Henry
- Kullmann, Dimitri M
- Baines, Richard A
- Usowicz, Maria M
- Krishnakumar, Shyam S
- Hodge, James J L
- Rothman, James E
- Jepson, James E C
Producer: 20180522
In:
Cell reports vol. 21
Availability: No items available.
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