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Single base resolution analysis of 5-hydroxymethylcytosine in 188 human genes: implications for hepatic gene expression. [electronic resource] by
- Ivanov, Maxim
- Kals, Mart
- Lauschke, Volker
- Barragan, Isabel
- Ewels, Philip
- Käller, Max
- Axelsson, Tomas
- Lehtiö, Janne
- Milani, Lili
- Ingelman-Sundberg, Magnus
Producer: 20170605
In:
Nucleic acids research vol. 44
Availability: No items available.
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CYP2W1 polymorphism: functional aspects and relation to risk for colorectal cancer. [electronic resource] by
- Stenstedt, Kristina
- Travica, Sandra
- Guo, Jia
- Barragan, Isabel
- Pors, Klaus
- Patterson, Laurence
- Edler, David
- Mkrtchian, Souren
- Johansson, Inger
- Ingelman-Sundberg, Magnus
Producer: 20140506
In:
Pharmacogenomics vol. 14
Availability: No items available.
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Long-term chronic toxicity testing using human pluripotent stem cell-derived hepatocytes. [electronic resource] by
- Holmgren, Gustav
- Sjögren, Anna-Karin
- Barragan, Isabel
- Sabirsh, Alan
- Sartipy, Peter
- Synnergren, Jane
- Björquist, Petter
- Ingelman-Sundberg, Magnus
- Andersson, Tommy B
- Edsbagge, Josefina
Producer: 20150330
In:
Drug metabolism and disposition: the biological fate of chemicals vol. 42
Availability: No items available.
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Copy-number variations in EYS: a significant event in the appearance of arRP. [electronic resource] by
- Pieras, Juan I
- Barragán, Isabel
- Borrego, Salud
- Audo, Isabelle
- González-Del Pozo, María
- Bernal, Sara
- Baiget, Montserrat
- Zeitz, Christina
- Bhattacharya, Shomi S
- Antiñolo, Guillermo
Producer: 20110930
In:
Investigative ophthalmology & visual science vol. 52
Availability: No items available.
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Identification of novel mutations in the ortholog of Drosophila eyes shut gene (EYS) causing autosomal recessive retinitis pigmentosa. [electronic resource] by
- Abd El-Aziz, Mai M
- O'Driscoll, Ciara A
- Kaye, Rebecca S
- Barragan, Isabel
- El-Ashry, Mohamed F
- Borrego, Salud
- Antiñolo, Guillermo
- Pang, Chi Pui
- Webster, Andrew R
- Bhattacharya, Shomi S
Producer: 20100820
In:
Investigative ophthalmology & visual science vol. 51
Availability: No items available.
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EYS is a major gene for rod-cone dystrophies in France. [electronic resource] by
- Audo, Isabelle
- Sahel, José-Alain
- Mohand-Saïd, Saddek
- Lancelot, Marie-Elise
- Antonio, Aline
- Moskova-Doumanova, Veselina
- Nandrot, Emeline F
- Doumanov, Jordan
- Barragan, Isabel
- Antinolo, Guillermo
- Bhattacharya, Shomi S
- Zeitz, Christina
Producer: 20100730
In:
Human mutation vol. 31
Availability: No items available.
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Microarray-based mutation analysis of 183 Spanish families with Usher syndrome. [electronic resource] by
- Jaijo, Teresa
- Aller, Elena
- García-García, Gema
- Aparisi, María J
- Bernal, Sara
- Avila-Fernández, Almudena
- Barragán, Isabel
- Baiget, Montserrat
- Ayuso, Carmen
- Antiñolo, Guillermo
- Díaz-Llopis, Manuel
- Külm, Maigi
- Beneyto, Magdalena
- Nájera, Carmen
- Millán, Jose M
Producer: 20100326
In:
Investigative ophthalmology & visual science vol. 51
Availability: No items available.
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Cytostatic Effect of Repeated Exposure to Simvastatin: A Mechanism for Chronic Myotoxicity Revealed by the Use of Mesodermal Progenitors Derived from Human Pluripotent Stem Cells. [electronic resource] by
- Peric, Delphine
- Barragan, Isabel
- Giraud-Triboult, Karine
- Egesipe, Anne-Laure
- Meyniel-Schicklin, Laurène
- Cousin, Christelle
- Lotteau, Vincent
- Petit, Vincent
- Touhami, Jawida
- Battini, Jean-Luc
- Sitbon, Marc
- Pinset, Christian
- Ingelman-Sundberg, Magnus
- Laustriat, Delphine
- Peschanski, Marc
Producer: 20160706
In:
Stem cells (Dayton, Ohio) vol. 33
Availability: No items available.
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20.
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Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa. [electronic resource] by
- Barragán, Isabel
- Borrego, Salud
- Pieras, Juan Ignacio
- González-del Pozo, María
- Santoyo, Javier
- Ayuso, Carmen
- Baiget, Montserrat
- Millan, José M
- Mena, Marcela
- Abd El-Aziz, Mai M
- Audo, Isabelle
- Zeitz, Christina
- Littink, Karin W
- Dopazo, Joaquín
- Bhattacharya, Shomi S
- Antiñolo, Guillermo
Producer: 20101216
In:
Human mutation vol. 31
Availability: No items available.
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