Author/Creator: Mornet, Etienne - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Mornet, Etienne

1. FRI0015 EXON 5 DUPLICATION IN ALPL GENE AS THE GENETIC CAUSE OF HYPOPHOSPATASIA IN A 3 YEAR OLD GIRL. (June 2019)

Authors:: González-Roca, Eva; Muñoz-Torres, Manuela; Carrasco, Pilar; González-Meneses, Antonio; Yahyaoui, Raquel; Isanta, Ricard; Mornet, Etienne
Journal:: Annals of the rheumatic diseases
Issue:: Volume 78(2019)Supplement 2
Page Start:: 668
Record Type:: Journal Article
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2. Identification of altered brain metabolites associated with TNAP activity in a mouse model of hypophosphatasia using untargeted NMR‐based metabolomics analysis. Issue 6 (5th March 2017)

Authors:: Cruz, Thomas; Gleizes, Marie; Balayssac, Stéphane; Mornet, Etienne; Marsal, Grégory; Millán, José Luis; Malet‐Martino, Myriam; Nowak, Lionel G; Gilard, Véronique; Fonta, Caroline
Journal:: Journal of neurochemistry
Issue:: Volume 140:Issue 6(2017)
Page Start:: 919
Record Type:: Journal Article
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3. Identification of altered brain metabolites associated with TNAP activity in a mouse model of hypophosphatasia using untargeted NMR‐based metabolomics analysis. Issue 6 (March 2017)

Authors:: Cruz, Thomas; Gleizes, Marie; Balayssac, Stéphane; Mornet, Etienne; Marsal, Grégory; Millán, José Luis; Malet‐Martino, Myriam; Nowak, Lionel G; Gilard, Véronique; Fonta, Caroline
Journal:: Journal of neurochemistry
Issue:: Volume 140:Issue 6(2017)
Page Start:: 919
Record Type:: Journal Article
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4. Large‐scale in vitro functional testing and novel variant scoring via protein modeling provide insights into alkaline phosphatase activity in hypophosphatasia. Issue 7 (18th March 2020)

Authors:: del Angel, Guillermo; Reynders, John; Negron, Christopher; Steinbrecher, Thomas; Mornet, Etienne
Journal:: Human mutation
Issue:: Volume 41:Issue 7(2020)
Page Start:: 1250
Record Type:: Journal Article
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