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J Millen

Showing results (151-160 of 167) with videos related to

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Plos Genetics|December 17, 2013
A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia miceJessica A Lehoczky, Peedikayil E Thomas, Kevin M Patrie, et al.
AJNR. American Journal of Neuroradiology|August 17, 2023
Dandy-Walker Phenotype with Brainstem Involvement: 2 Distinct Subgroups with Different PrognosisC A P F Alves, J Sidpra, A Manteghinejad, et al.
Human Mutation|May 16, 2013
Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephalocelesBenjamin W Darbro, Vinit B Mahajan, Lokesh Gakhar, et al.
Cerebellum (London, England)|February 29, 2012
Consensus paper: pathological role of the cerebellum in autismS Hossein Fatemi, Kimberly A Aldinger, Paul Ashwood, et al.
Cerebellum (London, England)|June 5, 2025
Conference Report: Cerebellar Development and Disease at Single-Cell ResolutionLena M Kutscher, Davide Aprile, N Sumru Bayin, et al.
Acta Neuropathologica|August 4, 2021
Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformationParthiv Haldipur, Silvia Bernardo, Kimberly A Aldinger, et al.
Breast Cancer Research and Treatment|October 4, 2024
Irish national real-world analysis of the clinical and economic impact of 21-gene oncotype DX® testing in early-stage, 1-3 lymph node-positive, oestrogen receptor-positive, HER2-negative, breast cancerI M Browne, R A McLaughlin, C S Weadick, et al.
Journal of Neurophysiology|May 18, 2022
Human <i>KCNQ5</i> de novo mutations underlie epilepsy and intellectual disabilityAguan D Wei, Paul Wakenight, Theresa A Zwingman, et al.
Cerebellum (London, England)|October 7, 2015
Consensus Paper: Cerebellar DevelopmentKetty Leto, Marife Arancillo, Esther B E Becker, et al.
Nature|September 21, 2022
Unified rhombic lip origins of group 3 and group 4 medulloblastomaKyle S Smith, Laure Bihannic, Brian L Gudenas, et al.
Pageof 17

Showing results (151-160 of 167) with videos related to

Sort By:
Pageof 17
Plos Genetics|December 17, 2013
A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia miceJessica A Lehoczky, Peedikayil E Thomas, Kevin M Patrie, et al.
AJNR. American Journal of Neuroradiology|August 17, 2023
Dandy-Walker Phenotype with Brainstem Involvement: 2 Distinct Subgroups with Different PrognosisC A P F Alves, J Sidpra, A Manteghinejad, et al.
Human Mutation|May 16, 2013
Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephalocelesBenjamin W Darbro, Vinit B Mahajan, Lokesh Gakhar, et al.
Cerebellum (London, England)|February 29, 2012
Consensus paper: pathological role of the cerebellum in autismS Hossein Fatemi, Kimberly A Aldinger, Paul Ashwood, et al.
Cerebellum (London, England)|June 5, 2025
Conference Report: Cerebellar Development and Disease at Single-Cell ResolutionLena M Kutscher, Davide Aprile, N Sumru Bayin, et al.
Acta Neuropathologica|August 4, 2021
Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformationParthiv Haldipur, Silvia Bernardo, Kimberly A Aldinger, et al.
Breast Cancer Research and Treatment|October 4, 2024
Irish national real-world analysis of the clinical and economic impact of 21-gene oncotype DX® testing in early-stage, 1-3 lymph node-positive, oestrogen receptor-positive, HER2-negative, breast cancerI M Browne, R A McLaughlin, C S Weadick, et al.
Journal of Neurophysiology|May 18, 2022
Human <i>KCNQ5</i> de novo mutations underlie epilepsy and intellectual disabilityAguan D Wei, Paul Wakenight, Theresa A Zwingman, et al.
Cerebellum (London, England)|October 7, 2015
Consensus Paper: Cerebellar DevelopmentKetty Leto, Marife Arancillo, Esther B E Becker, et al.
Nature|September 21, 2022
Unified rhombic lip origins of group 3 and group 4 medulloblastomaKyle S Smith, Laure Bihannic, Brian L Gudenas, et al.
Pageof 17