Results
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45181.
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A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor. [electronic resource] by
- Ramser, Juliane
- Abidi, Fatima E
- Burckle, Celine A
- Lenski, Claus
- Toriello, Helga
- Wen, Gaiping
- Lubs, Herbert A
- Engert, Stefanie
- Stevenson, Roger E
- Meindl, Alfons
- Schwartz, Charles E
- Nguyen, Genevieve
Producer: 20050816
In:
Human molecular genetics vol. 14
Availability: No items available.
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45182.
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45183.
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45184.
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45185.
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45186.
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45187.
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45188.
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45189.
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45190.
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45191.
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45192.
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45193.
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Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study. [electronic resource] by
- Pfeufer, Arne
- Jalilzadeh, Shapour
- Perz, Siegfried
- Mueller, Jakob C
- Hinterseer, Martin
- Illig, Thomas
- Akyol, Mahmut
- Huth, Cornelia
- Schöpfer-Wendels, Andreas
- Kuch, Bernhard
- Steinbeck, Gerhard
- Holle, Rolf
- Näbauer, Michael
- Wichmann, H-Erich
- Meitinger, Thomas
- Kääb, Stefan
Producer: 20050922
In:
Circulation research vol. 96
Availability: No items available.
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45194.
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45195.
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45196.
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45197.
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45198.
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45199.
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45200.
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Isolation and characterization of human antigen-specific TCR alpha beta+ CD4(-)CD8- double-negative regulatory T cells. [electronic resource] by
- Fischer, Karin
- Voelkl, Simon
- Heymann, Jana
- Przybylski, Grzegorz K
- Mondal, Krishna
- Laumer, Monika
- Kunz-Schughart, Leoni
- Schmidt, Christian A
- Andreesen, Reinhard
- Mackensen, Andreas
Producer: 20050503
In:
Blood vol. 105
Availability: No items available.
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