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Carol-Anne Martin

Showing results (1-10 of 17) with videos related to

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Journal of Cell Science|August 3, 2013
Meeting report - building a centrosomeAlexandre D Baffet, Carol-Anne Martin, Ilaria Scarfone, et al.
Nature|September 3, 2013
Cerebral organoids model human brain development and microcephalyMadeline A Lancaster, Magdalena Renner, Carol-Anne Martin, et al.
Nature Genetics|December 25, 2007
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signalingElen Griffith, Sarah Walker, Carol-Anne Martin, et al.
Nature Genetics|March 2, 2011
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndromeLouise S Bicknell, Sarah Walker, Anna Klingseisen, et al.
American Journal of Ophthalmology|May 12, 2019
Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With MicrocephalySarah Hull, Gavin Arno, Pia Ostergaard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2020
Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathyDavid A Parry, Carol-Anne Martin, Philip Greene, et al.
Nature|July 25, 2017
cGAS surveillance of micronuclei links genome instability to innate immunityKaren J Mackenzie, Paula Carroll, Carol-Anne Martin, et al.
Genes & Development|June 2, 2017
Corrigendum: Mutations in genes encoding condensins cause microcephaly through decatenation failure at mitosisCarol-Anne Martin, Jennie E Murray, Paula Carroll, et al.
Nature Genetics|November 28, 2018
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regionsPatricia Heyn, Clare V Logan, Adeline Fluteau, et al.
Genes & Development|October 15, 2016
Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosisCarol-Anne Martin, Jennie E Murray, Paula Carroll, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Journal of Cell Science|August 3, 2013
Meeting report - building a centrosomeAlexandre D Baffet, Carol-Anne Martin, Ilaria Scarfone, et al.
Nature|September 3, 2013
Cerebral organoids model human brain development and microcephalyMadeline A Lancaster, Magdalena Renner, Carol-Anne Martin, et al.
Nature Genetics|December 25, 2007
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signalingElen Griffith, Sarah Walker, Carol-Anne Martin, et al.
Nature Genetics|March 2, 2011
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndromeLouise S Bicknell, Sarah Walker, Anna Klingseisen, et al.
American Journal of Ophthalmology|May 12, 2019
Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With MicrocephalySarah Hull, Gavin Arno, Pia Ostergaard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2020
Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathyDavid A Parry, Carol-Anne Martin, Philip Greene, et al.
Nature|July 25, 2017
cGAS surveillance of micronuclei links genome instability to innate immunityKaren J Mackenzie, Paula Carroll, Carol-Anne Martin, et al.
Genes & Development|June 2, 2017
Corrigendum: Mutations in genes encoding condensins cause microcephaly through decatenation failure at mitosisCarol-Anne Martin, Jennie E Murray, Paula Carroll, et al.
Nature Genetics|November 28, 2018
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regionsPatricia Heyn, Clare V Logan, Adeline Fluteau, et al.
Genes & Development|October 15, 2016
Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosisCarol-Anne Martin, Jennie E Murray, Paula Carroll, et al.
Pageof 2