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Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline
Authors: Pulvers, Jeremy N.; Bryk, Jarosław; Fish, Jennifer L.; Wilsch-Bräuninger, Michaela; Arai, Yoko; Schreier, Dora; Naumann, Ronald; Helppi, Jussi; Habermann, Bianca; Vogt, Johannes; Nitsch, Robert; Tóth, Attila; Enard, Wolfgang; Pääbo, Svante; Huttner, Wieland B.
Date of Publication (YYYY-MM-DD): 2010-09-21
Title of Journal: Proceedings of the National Academy of Sciences of the United States of America
Volume: 107
Issue / Number: 38
Start Page: 16595
End Page: 16600
Document Type: Article
ID: 572151.0
 
Full text / Content available
Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline
Authors: Pulvers, Jeremy N.; Bryk, Jarosław; Fish, Jennifer L.; Wilsch-Bräuninger, Michaela; Arai, Yoko; Schreier, Dora; Naumann, Ronald; Helppi, Jussi; Habermann, Bianca; Vogt, Johannes; Nitsch, Robert; Tóth, Attila; Enard, Wolfgang; Pääbo, Svante; Huttner, Wieland B.
Date of Publication (YYYY-MM-DD): 2010
Title of Journal: Proceedings of the National Academy of Sciences of the United States of America
Volume: 107
Issue / Number: 38
Start Page: 16595
End Page: 16600
Document Type: Article
ID: 499377.0
Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline.
Authors: Pulvers, Jeremy N.; Bryk, Jaroslaw; Fish, Jennifer L.; Wilsch-Bräuninger, Michaela; Arai, Yoko; Schreier, Dora; Naumann, Ronald; Helppi, Jussi; Habermann, Bianca; Vogt, Johannes; Nitsch, Robert; Toth, Attila; Enard, Wolfgang; Pääbo, Svante; Huttner, Wieland B.
Date of Publication (YYYY-MM-DD): 2010
Title of Journal: Proceedings of the National Academy of Sciences of the United States of America
Volume: 107
Issue / Number: 38
Start Page: 16595
End Page: 16600
Document Type: Article
ID: 546629.0
Mouse HORMAD1 and HORMAD2, two conserved meiotic chromosomal proteins, are depleted from synapsed chromosome axes with the help of TRIP13 AAA-ATPase
Authors: Wojtasz, Lukasz; Daniel, Katrin; Roig, Ignasi; Bolcun-Filas, Ewelina; Xu, Huiling; Boonsanay, Verawan; Eckmann, Christian R; Cooke, Howard J; Jasin, Maria; Keeney, Scott; McKay, Michael J; Toth, Attila
Date of Publication (YYYY-MM-DD): 2009
Title of Journal: PLoS Genetics
Volume: 5
Issue / Number: 10
Start Page: 1000702-1
End Page: 1000702-28
Document Type: Article
ID: 463218.0
Entries: 1-4  
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