scholarly journals Author response: Alterations of specific cortical GABAergic circuits underlie abnormal network activity in a mouse model of Down syndrome

2020 ◽  
Author(s):  
Javier Zorrilla de San Martin ◽  
Cristina Donato ◽  
Jérémy Peixoto ◽  
Andrea Aguirre ◽  
Vikash Choudhary ◽  
...  
Keyword(s):  
Down Syndrome ◽  
Mouse Model ◽  
Network Activity ◽  
Author Response

scholarly journals Author response: A non-mosaic transchromosomic mouse model of Down syndrome carrying the long arm of human chromosome 21

2020 ◽  
Author(s):  
Yasuhiro Kazuki ◽  
Feng J Gao ◽  
Yicong Li ◽  
Anna J Moyer ◽  
Benjamin Devenney ◽  
...  
Keyword(s):  
Down Syndrome ◽  
Mouse Model ◽  
Human Chromosome ◽  
Chromosome 21 ◽  
Author Response ◽  
Human Chromosome 21

scholarly journals Author response: Alterations of in vivo CA1 network activity in Dp(16)1Yey Down syndrome model mice

2017 ◽  
Author(s):  
Matthieu Raveau ◽  
Denis Polygalov ◽  
Roman Boehringer ◽  
Kenji Amano ◽  
Kazuhiro Yamakawa ◽  
...  
Keyword(s):  
Down Syndrome ◽  
Network Activity ◽  
Author Response

scholarly journals Perturbation of fetal hematopoiesis in a mouse model of Down syndrome’s transient myeloproliferative disorder

Blood ◽  
2013 ◽  
Vol 122 (6) ◽  
pp. 988-998 ◽  
Author(s):  
Yehudit Birger ◽  
Liat Goldberg ◽  
Timothy M. Chlon ◽  
Benjamin Goldenson ◽  
Inna Muler ◽  
...  
Keyword(s):  
Down Syndrome ◽  
Mouse Model ◽  
Myeloproliferative Disorder ◽  
Transient Myeloproliferative Disorder ◽  
Terminal Domain ◽  
Key Points ◽  
Fetal Hematopoiesis ◽  
Fetal Erythropoiesis

Key Points Transient expansion of fetal megaerythroid progenitors in ERG/Gata1s mouse is biologically similar to Down syndrome TMD. The N-terminal domain of GATA1 and the downregulation of ERG expression are essential for normal fetal erythropoiesis.

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