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J Ingham

Showing results (271-280 of 283) with videos related to

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EMBO Molecular Medicine|February 17, 2016
Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearingAnnalisa Buniello, Neil J Ingham, Morag A Lewis, et al.
Blood|November 8, 2018
Acute myeloid leukemia induces protumoral p16INK4a-driven senescence in the bone marrow microenvironmentAmina M Abdul-Aziz, Yu Sun, Charlotte Hellmich, et al.
Plos Biology|April 12, 2019
Mouse screen reveals multiple new genes underlying mouse and human hearing lossNeil J Ingham, Selina A Pearson, Valerie E Vancollie, et al.
JCI Insight|February 8, 2022
The timing of auditory sensory deficits in Norrie disease has implications for therapeutic interventionDale Bryant, Valda Pauzuolyte, Neil J Ingham, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2022
Mutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and miceGuney Bademci, María Lachgar-Ruiz, Mangesh Deokar, et al.
Molecular and Cellular Biology|August 2, 2005
WW domains provide a platform for the assembly of multiprotein networksRobert J Ingham, Karen Colwill, Caley Howard, et al.
Plos One|May 19, 2012
A multi-platform flow device for microbial (co-) cultivation and microscopic analysisMatthijn C Hesselman, Dorett I Odoni, Brendan M Ryback, et al.
Cell|July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesJacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
American Journal of Human Genetics|December 4, 2012
Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndromeLina Basel-Vanagaite, Bruno Dallapiccola, Ramiro Ramirez-Solis, et al.
Nucleic Acids Research|November 5, 2020
Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdropletsTim J Puchtler, Kerr Johnson, Rebecca N Palmer, et al.
Pageof 29

Showing results (271-280 of 283) with videos related to

Sort By:
Pageof 29
EMBO Molecular Medicine|February 17, 2016
Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearingAnnalisa Buniello, Neil J Ingham, Morag A Lewis, et al.
Blood|November 8, 2018
Acute myeloid leukemia induces protumoral p16INK4a-driven senescence in the bone marrow microenvironmentAmina M Abdul-Aziz, Yu Sun, Charlotte Hellmich, et al.
Plos Biology|April 12, 2019
Mouse screen reveals multiple new genes underlying mouse and human hearing lossNeil J Ingham, Selina A Pearson, Valerie E Vancollie, et al.
JCI Insight|February 8, 2022
The timing of auditory sensory deficits in Norrie disease has implications for therapeutic interventionDale Bryant, Valda Pauzuolyte, Neil J Ingham, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 2022
Mutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and miceGuney Bademci, María Lachgar-Ruiz, Mangesh Deokar, et al.
Molecular and Cellular Biology|August 2, 2005
WW domains provide a platform for the assembly of multiprotein networksRobert J Ingham, Karen Colwill, Caley Howard, et al.
Plos One|May 19, 2012
A multi-platform flow device for microbial (co-) cultivation and microscopic analysisMatthijn C Hesselman, Dorett I Odoni, Brendan M Ryback, et al.
Cell|July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesJacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
American Journal of Human Genetics|December 4, 2012
Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndromeLina Basel-Vanagaite, Bruno Dallapiccola, Ramiro Ramirez-Solis, et al.
Nucleic Acids Research|November 5, 2020
Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdropletsTim J Puchtler, Kerr Johnson, Rebecca N Palmer, et al.
Pageof 29