J
Jeremy N. Pulvers
Researcher at University of Sydney
Publications - 10
Citations - 1068
Jeremy N. Pulvers is an academic researcher from University of Sydney. The author has contributed to research in topics: Neuroepithelial cell & Progenitor cell. The author has an hindex of 7, co-authored 9 publications receiving 947 citations. Previous affiliations of Jeremy N. Pulvers include Max Planck Society.
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Journal ArticleDOI
miRNAs are essential for survival and differentiation of newborn neurons but not for expansion of neural progenitors during early neurogenesis in the mouse embryonic neocortex
Davide De Pietri Tonelli,Jeremy N. Pulvers,Christiane Haffner,Elizabeth P. Murchison,Gregory J. Hannon,Wieland B. Huttner +5 more
TL;DR: The results support the emerging concept that progenitors are less dependent on miRNAs than their differentiated progeny, and raise interesting perspectives as to the expansion of somatic stem cells.
Journal ArticleDOI
Neural stem and progenitor cells shorten S-phase on commitment to neuron production.
Yoko Arai,Jeremy N. Pulvers,Christiane Haffner,Britta Schilling,Ina Nüsslein,Federico Calegari,Wieland B. Huttner +6 more
TL;DR: A novel approach to determine cell-cycle parameters in specific classes of neural stem and progenitor cells, identified by molecular markers rather than location, found that G1 lengthening was associated with the transition from stem cell-like apical progenitors to fate-restricted basal (intermediate) progensitors.
Journal ArticleDOI
Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline.
Jeremy N. Pulvers,Jarosław Bryk,Jennifer L. Fish,Michaela Wilsch-Bräuninger,Yoko Arai,Dora Schreier,Ronald Naumann,Jussi Helppi,Bianca Habermann,Johannes Vogt,Robert Nitsch,Attila Tóth,Wolfgang Enard,Svante Pääbo,Wieland B. Huttner +14 more
TL;DR: It is reported that in Aspm mutant mice, truncated Aspm proteins similar to those causing microcephaly in humans fail to localize to the midbody during M-phase and cause mild microCEphaly, which raises the possibility that positive selection of ASPM during primate evolution reflects its function in the germline.
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Brca1 is required for embryonic development of the mouse cerebral cortex to normal size by preventing apoptosis of early neural progenitors
TL;DR: The results show that Brca1 is required for the cerebral cortex to develop to normal size by preventing the apoptosis of early cortical progenitors and their immediate progeny.
Journal ArticleDOI
If Time Is Brain Where Is the Improvement in Prehospital Time after Stroke
TL;DR: Major factors affecting prehospital time were related to emergency medical pathways, stroke symptomatology, patient and bystander behavior, patient health characteristics, and stroke treatment awareness, and interventions addressing these factors may prove effective in reducing prehospital delay.