Results
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7741.
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7742.
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7743.
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7744.
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7745.
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7746.
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7747.
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7748.
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7749.
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7750.
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7751.
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Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption. [electronic resource] by
- Qiu, Andong
- Jansen, Michaela
- Sakaris, Antoinette
- Min, Sang Hee
- Chattopadhyay, Shrikanta
- Tsai, Eugenia
- Sandoval, Claudio
- Zhao, Rongbao
- Akabas, Myles H
- Goldman, I David
Producer: 20070109
In:
Cell vol. 127
Availability: No items available.
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7752.
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7753.
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7754.
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7755.
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Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption. [electronic resource] by
- Mahadeo, Kris
- Diop-Bove, Ndeye
- Shin, Daniel
- Unal, Ersin Selcuk
- Teo, Juliana
- Zhao, Rongbao
- Chang, Min-Hwang
- Fulterer, Andreas
- Romero, Michael F
- Goldman, I David
Producer: 20101122
In:
American journal of physiology. Cell physiology vol. 299
Availability: No items available.
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7756.
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7757.
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7758.
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Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form. [electronic resource] by
- Salomon, Julie
- Goulet, Olivier
- Canioni, Danielle
- Brousse, Nicole
- Lemale, Julie
- Tounian, Patrick
- Coulomb, Aurore
- Marinier, Evelyne
- Hugot, Jean-Pierre
- Ruemmele, Frank
- Dufier, Jean-Louis
- Roche, Olivier
- Bodemer, Christine
- Colomb, Virginie
- Talbotec, Cécile
- Lacaille, Florence
- Campeotto, Florence
- Cerf-Bensussan, Nadine
- Janecke, Andreas R
- Mueller, Thomas
- Koletzko, Sibylle
- Bonnefont, Jean-Paul
- Lyonnet, Stanislas
- Munnich, Arnold
- Poirier, Françoise
- Smahi, Asma
Producer: 20140407
In:
Human genetics vol. 133
Availability: No items available.
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7759.
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7760.
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