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Regulation of ClC-2 gating by intracellular ATP. [electronic resource] by
- Stölting, Gabriel
- Teodorescu, Georgeta
- Begemann, Birgit
- Schubert, Julian
- Nabbout, Rima
- Toliat, Mohammad Reza
- Sander, Thomas
- Nürnberg, Peter
- Lerche, Holger
- Fahlke, Christoph
Producer: 20140403
In:
Pflugers Archiv : European journal of physiology vol. 465
Availability: No items available.
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10.
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Plasma vascular endothelial growth Factor-A (VEGF-A) and VEGF-A gene polymorphism are associated with hydrocele development in lymphatic filariasis. [electronic resource] by
- Debrah, Alexander Yaw
- Mand, Sabine
- Toliat, Mohammad Reza
- Marfo-Debrekyei, Yeboah
- Batsa, Linda
- Nürnberg, Peter
- Lawson, Bernard
- Adjei, Ohene
- Hoerauf, Achim
- Pfarr, Kenneth
Producer: 20071211
In:
The American journal of tropical medicine and hygiene vol. 77
Availability: No items available.
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11.
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Replication of genetic susceptibility loci for testicular germ cell cancer in the Croatian population. [electronic resource] by
- Lessel, Davor
- Gamulin, Marija
- Kulis, Tomislav
- Toliat, Mohammad Reza
- Grgic, Mislav
- Friedrich, Katrin
- Zunec, Renata
- Balija, Melita
- Nürnberg, Peter
- Kastelan, Zeljko
- Högel, Josef
- Kubisch, Christian
Producer: 20121105
In:
Carcinogenesis vol. 33
Availability: No items available.
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12.
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Polymorphisms in the chemokine (C-X-C motif) ligand 10 are associated with invasive aspergillosis after allogeneic stem-cell transplantation and influence CXCL10 expression in monocyte-derived dendritic cells. [electronic resource] by
- Mezger, Markus
- Steffens, Michael
- Beyer, Melanie
- Manger, Carolin
- Eberle, Johannes
- Toliat, Mohammad-Reza
- Wienker, Thomas F
- Ljungman, Per
- Hebart, Holger
- Dornbusch, Hans Jürgen
- Einsele, Hermann
- Loeffler, Juergen
Producer: 20080311
In:
Blood vol. 111
Availability: No items available.
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13.
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Lack of association between 71 variations located in candidate genes and response to acute haloperidol treatment. [electronic resource] by
- Giegling, Ina
- Drago, Antonio
- Schäfer, Martin
- Hartmann, Annette M
- Sander, Thomas
- Toliat, Mohammad Reza
- Möller, Hans-Jürgen
- De Ronchi, Diana
- Stassen, Hans H
- Rujescu, Dan
- Serretti, Alessandro
Producer: 20110714
In:
Psychopharmacology vol. 214
Availability: No items available.
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14.
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Haplotypes and SNPs in 13 lipid-relevant genes explain most of the genetic variance in high-density lipoprotein and low-density lipoprotein cholesterol. [electronic resource] by
- Knoblauch, Hans
- Bauerfeind, Anja
- Toliat, Mohammad Reza
- Becker, Christian
- Luganskaja, Tatjana
- Günther, Ulf Peter
- Rohde, Klaus
- Schuster, Herbert
- Junghans, Christine
- Luft, Friedrich C
- Nürnberg, Peter
- Reich, Jens Georg
Producer: 20041216
In:
Human molecular genetics vol. 13
Availability: No items available.
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15.
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Glutamatergic gene variants impact the clinical profile of efficacy and side effects of haloperidol. [electronic resource] by
- Giegling, Ina
- Drago, Antonio
- Dolžan, Vita
- Plesničar, Blanka Kores
- Schäfer, Martin
- Hartmann, Annette M
- Sander, Thomas
- Toliat, Mohammad Reza
- Möller, Hans-Jürgen
- Stassen, Hans H
- Rujescu, Dan
- Serretti, Alessandro
Producer: 20110722
In:
Pharmacogenetics and genomics vol. 21
Availability: No items available.
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16.
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Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantation. [electronic resource] by
- Loeffler, Juergen
- Steffens, Michael
- Arlt, Eva-Maria
- Toliat, Mohammad-Reza
- Mezger, Markus
- Suk, Anita
- Wienker, Thomas F
- Hebart, Holger
- Nürnberg, Peter
- Boeckh, Michael
- Ljungman, Per
- Trenschel, Rudolf
- Einsele, Hermann
Producer: 20060727
In:
Journal of clinical microbiology vol. 44
Availability: No items available.
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17.
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Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease. [electronic resource] by
- Rakovic, Aleksandar
- Stiller, Barbara
- Djarmati, Ana
- Flaquer, Antonia
- Freudenberg, Jan
- Toliat, Mohammad-Reza
- Linnebank, Michael
- Kostic, Vladimir
- Lohmann, Katja
- Paus, Sebastian
- Nürnberg, Peter
- Kubisch, Christian
- Klein, Christine
- Wüllner, Ullrich
- Ramirez, Alfredo
Producer: 20090727
In:
Movement disorders : official journal of the Movement Disorder Society vol. 24
Availability: No items available.
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18.
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Meta-Analysis of Genome-Wide Association Studies and Network Analysis-Based Integration with Gene Expression Data Identify New Suggestive Loci and Unravel a Wnt-Centric Network Associated with Dupuytren's Disease. [electronic resource] by
- Becker, Kerstin
- Siegert, Sabine
- Toliat, Mohammad Reza
- Du, Juanjiangmeng
- Casper, Ramona
- Dolmans, Guido H
- Werker, Paul M
- Tinschert, Sigrid
- Franke, Andre
- Gieger, Christian
- Strauch, Konstantin
- Nothnagel, Michael
- Nürnberg, Peter
- Hennies, Hans Christian
Producer: 20170726
In:
PloS one vol. 11
Availability: No items available.
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19.
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Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism. [electronic resource] by
- Rutsch, Frank
- Gailus, Susann
- Miousse, Isabelle R
- Suormala, Terttu
- Sagné, Corinne
- Toliat, Mohammad Reza
- Nürnberg, Gudrun
- Wittkampf, Tanja
- Buers, Insa
- Sharifi, Azita
- Stucki, Martin
- Becker, Christian
- Baumgartner, Matthias
- Robenek, Horst
- Marquardt, Thorsten
- Höhne, Wolfgang
- Gasnier, Bruno
- Rosenblatt, David S
- Fowler, Brian
- Nürnberg, Peter
Producer: 20090213
In:
Nature genetics vol. 41
Availability: No items available.
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20.
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Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1. [electronic resource] by
- Crisponi, Laura
- Crisponi, Giangiorgio
- Meloni, Alessandra
- Toliat, Mohammad Reza
- Nurnberg, Gudrun
- Usala, Gianluca
- Uda, Manuela
- Masala, Marco
- Hohne, Wolfgang
- Becker, Christian
- Marongiu, Mara
- Chiappe, Francesca
- Kleta, Robert
- Rauch, Anita
- Wollnik, Bernd
- Strasser, Friedrich
- Reese, Thomas
- Jakobs, Cornelis
- Kurlemann, Gerd
- Cao, Antonio
- Nurnberg, Peter
- Rutsch, Frank
Producer: 20070611
In:
American journal of human genetics vol. 80
Availability: No items available.
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