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Serological autoantibody profiling of type 1 diabetes by protein arrays. [electronic resource] by
- Miersch, Shane
- Bian, Xiaofang
- Wallstrom, Garrick
- Sibani, Sahar
- Logvinenko, Tanya
- Wasserfall, Clive H
- Schatz, Desmond
- Atkinson, Mark
- Qiu, Ji
- LaBaer, Joshua
Producer: 20140722
In:
Journal of proteomics vol. 94
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64.
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65.
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Impaired development of neocortical circuits contributes to the neurological alterations in DYRK1A haploinsufficiency syndrome. [electronic resource] by
- Arranz, Juan
- Balducci, Elisa
- Arató, Krisztina
- Sánchez-Elexpuru, Gentzane
- Najas, Sònia
- Parras, Alberto
- Rebollo, Elena
- Pijuan, Isabel
- Erb, Ionas
- Verde, Gaetano
- Sahun, Ignasi
- Barallobre, Maria J
- Lucas, José J
- Sánchez, Marina P
- de la Luna, Susana
- Arbonés, Maria L
Producer: 20200109
In:
Neurobiology of disease vol. 127
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Natural aristolactams and aporphine alkaloids as inhibitors of CDK1/cyclin B and DYRK1A. [electronic resource] by
- Marti, Guillaume
- Eparvier, Véronique
- Morleo, Barbara
- Le Ven, Jessica
- Apel, Cécile
- Bodo, Bernard
- Amand, Séverine
- Dumontet, Vincent
- Lozach, Olivier
- Meijer, Laurent
- Guéritte, Françoise
- Litaudon, Marc
Producer: 20130830
In:
Molecules (Basel, Switzerland) vol. 18
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LncRNA OIP5-AS1 regulates radioresistance by targeting DYRK1A through miR-369-3p in colorectal cancer cells. [electronic resource] by
- Zou, Yanmei
- Yao, Shuo
- Chen, Xiuqiong
- Liu, Dian
- Wang, Jianhua
- Yuan, Xun
- Rao, Jie
- Xiong, Huihua
- Yu, Shiying
- Yuan, Xianglin
- Zhu, Feng
- Hu, Guohong
- Wang, Yihua
- Xiong, Hua
Producer: 20181024
In:
European journal of cell biology vol. 97
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Development of Kinase Inhibitors via Metal-Catalyzed C⁻H Arylation of 8-Alkyl-thiazolo[5,4- [electronic resource] by
- Couly, Florence
- Harari, Marine
- Dubouilh-Benard, Carole
- Bailly, Laetitia
- Petit, Emilie
- Diharce, Julien
- Bonnet, Pascal
- Meijer, Laurent
- Fruit, Corinne
- Besson, Thierry
Producer: 20181112
In:
Molecules (Basel, Switzerland) vol. 23
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DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies. [electronic resource] by
- Ji, Jianling
- Lee, Hane
- Argiropoulos, Bob
- Dorrani, Naghmeh
- Mann, John
- Martinez-Agosto, Julian A
- Gomez-Ospina, Natalia
- Gallant, Natalie
- Bernstein, Jonathan A
- Hudgins, Louanne
- Slattery, Leah
- Isidor, Bertrand
- Le Caignec, Cédric
- David, Albert
- Obersztyn, Ewa
- Wiśniowiecka-Kowalnik, Barbara
- Fox, Michelle
- Deignan, Joshua L
- Vilain, Eric
- Hendricks, Emily
- Horton Harr, Margaret
- Noon, Sarah E
- Jackson, Jessi R
- Wilkens, Alisha
- Mirzaa, Ghayda
- Salamon, Noriko
- Abramson, Jeff
- Zackai, Elaine H
- Krantz, Ian
- Innes, A Micheil
- Nelson, Stanley F
- Grody, Wayne W
- Quintero-Rivera, Fabiola
Producer: 20160506
In:
European journal of human genetics : EJHG vol. 23
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