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Exploring Genetic Factors Involved in Huntington Disease Age of Onset: E2F2 as a New Potential Modifier Gene. [electronic resource] by
- Valcárcel-Ocete, Leire
- Alkorta-Aranburu, Gorka
- Iriondo, Mikel
- Fullaondo, Asier
- García-Barcina, María
- Fernández-García, José Manuel
- Lezcano-García, Elena
- Losada-Domingo, José María
- Ruiz-Ojeda, Javier
- Álvarez de Arcaya, Amaia
- Pérez-Ramos, José María
- Roos, Raymund A C
- Nielsen, Jørgen E
- Saft, Carsten
- Zubiaga, Ana M
- Aguirre, Ana
Producer: 20160330
In:
PloS one vol. 10
Availability: No items available.
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Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis. [electronic resource] by
- Emond, Mary J
- Louie, Tin
- Emerson, Julia
- Chong, Jessica X
- Mathias, Rasika A
- Knowles, Michael R
- Rieder, Mark J
- Tabor, Holly K
- Nickerson, Debbie A
- Barnes, Kathleen C
- Go, Lung
- Gibson, Ronald L
- Bamshad, Michael J
Producer: 20160610
In:
PLoS genetics vol. 11
Availability: No items available.
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87.
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Blood co-expression modules identify potential modifier genes of diabetes and lung function in cystic fibrosis. [electronic resource] by
- Pineau, Fanny
- Caimmi, Davide
- Magalhães, Milena
- Fremy, Enora
- Mohamed, Abdillah
- Mely, Laurent
- Leroy, Sylvie
- Murris, Marlène
- Claustres, Mireille
- Chiron, Raphael
- De Sario, Albertina
Producer: 20200720
In:
PloS one vol. 15
Availability: No items available.
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An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients. [electronic resource] by
- Bonnet, Crystel
- Riahi, Zied
- Chantot-Bastaraud, Sandra
- Smagghe, Luce
- Letexier, Mélanie
- Marcaillou, Charles
- Lefèvre, Gaëlle M
- Hardelin, Jean-Pierre
- El-Amraoui, Aziz
- Singh-Estivalet, Amrit
- Mohand-Saïd, Saddek
- Kohl, Susanne
- Kurtenbach, Anne
- Sliesoraityte, Ieva
- Zobor, Ditta
- Gherbi, Souad
- Testa, Francesco
- Simonelli, Francesca
- Banfi, Sandro
- Fakin, Ana
- Glavač, Damjan
- Jarc-Vidmar, Martina
- Zupan, Andrej
- Battelino, Saba
- Martorell Sampol, Loreto
- Claveria, Maria Antonia
- Catala Mora, Jaume
- Dad, Shzeena
- Møller, Lisbeth B
- Rodriguez Jorge, Jesus
- Hawlina, Marko
- Auricchio, Alberto
- Sahel, José-Alain
- Marlin, Sandrine
- Zrenner, Eberhart
- Audo, Isabelle
- Petit, Christine
Producer: 20170711
In:
European journal of human genetics : EJHG vol. 24
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92.
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TAS2R38 is a novel modifier gene in patients with cystic fibrosis. [electronic resource] by
- Castaldo, Alice
- Cernera, Gustavo
- Iacotucci, Paola
- Cimbalo, Chiara
- Gelzo, Monica
- Comegna, Marika
- Di Lullo, Antonella Miriam
- Tosco, Antonella
- Carnovale, Vincenzo
- Raia, Valeria
- Amato, Felice
Producer: 20201124
In:
Scientific reports vol. 10
Availability: No items available.
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95.
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Multi-OMICS analyses unveil [electronic resource] by
- Carapito, Raphael
- Carapito, Christine
- Morlon, Aurore
- Paul, Nicodème
- Vaca Jacome, Alvaro Sebastian
- Alsaleh, Ghada
- Rolli, Véronique
- Tahar, Ouria
- Aouadi, Ismail
- Rompais, Magali
- Delalande, François
- Pichot, Angélique
- Georgel, Philippe
- Messer, Laurent
- Sibilia, Jean
- Cianferani, Sarah
- Van Dorsselaer, Alain
- Bahram, Seiamak
Producer: 20190903
In:
Annals of the rheumatic diseases vol. 77
Availability: No items available.
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96.
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SPP1 genotype and glucocorticoid treatment modify osteopontin expression in Duchenne muscular dystrophy cells. [electronic resource] by
- Vianello, Sara
- Pantic, Boris
- Fusto, Aurora
- Bello, Luca
- Galletta, Eva
- Borgia, Doriana
- Gavassini, Bruno F
- Semplicini, Claudio
- Sorarù, Gianni
- Vitiello, Libero
- Pegoraro, Elena
Producer: 20180111
In:
Human molecular genetics vol. 26
Availability: No items available.
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