Results
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495281.
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495282.
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495283.
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495284.
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495285.
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A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If). [electronic resource] by
- Kranz, C
- Denecke, J
- Lehrman, M A
- Ray, S
- Kienz, P
- Kreissel, G
- Sagi, D
- Peter-Katalinic, J
- Freeze, H H
- Schmid, T
- Jackowski-Dohrmann, S
- Harms, E
- Marquardt, T
Producer: 20020103
In:
The Journal of clinical investigation vol. 108
Availability: No items available.
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495286.
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MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If. [electronic resource] by
- Schenk, B
- Imbach, T
- Frank, C G
- Grubenmann, C E
- Raymond, G V
- Hurvitz, H
- Korn-Lubetzki, I
- Revel-Vik, S
- Raas-Rotschild, A
- Luder, A S
- Jaeken, J
- Berger, E G
- Matthijs, G
- Hennet, T
- Aebi, M
Producer: 20020103
In:
The Journal of clinical investigation vol. 108
Availability: No items available.
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495287.
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Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings. [electronic resource] by
- Bronsveld, I
- Mekus, F
- Bijman, J
- Ballmann, M
- de Jonge, H R
- Laabs, U
- Halley, D J
- Ellemunter, H
- Mastella, G
- Thomas, S
- Veeze, H J
- Tümmler, B
Producer: 20020103
In:
The Journal of clinical investigation vol. 108
Availability: No items available.
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495288.
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495289.
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495290.
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Maturation of marginal zone and follicular B cells requires B cell activating factor of the tumor necrosis factor family and is independent of B cell maturation antigen. [electronic resource] by
- Schneider, P
- Takatsuka, H
- Wilson, A
- Mackay, F
- Tardivel, A
- Lens, S
- Cachero, T G
- Finke, D
- Beermann, F
- Tschopp, J
Producer: 20020111
In:
The Journal of experimental medicine vol. 194
Availability: No items available.
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495291.
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495292.
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495293.
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495294.
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495295.
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495296.
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495297.
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495298.
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495299.
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495300.
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