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J Byrd

Showing results (201-210 of 236) with videos related to

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Genomics|June 1, 1994
A physical map across chromosome 11q22-q23 containing the major locus for ataxia telangiectasiaH J Ambrose, P J Byrd, C M McConville, et al.
Analytical Chemistry|May 25, 2026
Nanopipettes Enable Native Mass Spectrometry Studies of the Intrinsically Disordered Protein α-Synuclein in Biochemical BuffersEmily J Byrd, Emma L Norgate, Joel A Crossley, et al.
Genomics|February 1, 1993
Irradiation hybrids for human chromosome 11: characterization and use for generating region-specific markers in 11q14-q23G T Gillett, C M McConville, P J Byrd, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 18, 2007
RIDDLE immunodeficiency syndrome is linked to defects in 53BP1-mediated DNA damage signalingGrant S Stewart, Tatjana Stankovic, Philip J Byrd, et al.
Cell|December 28, 1999
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorderG S Stewart, R S Maser, T Stankovic, et al.
Journal of Virology|December 17, 2010
Serotype-specific inactivation of the cellular DNA damage response during adenovirus infectionNatalie A Forrester, Garry G Sedgwick, Anoushka Thomas, et al.
Ophthalmology|September 1, 1991
Central photorefractive keratectomy for myopia. Partially sighted and normally sighted eyesM B McDonald, J C Liu, T J Byrd, et al.
Allergy and Asthma Proceedings|December 10, 2016
A comparison of seasonal trends in asthma exacerbations among children from geographic regions with different climatesJulia A Wisniewski, Anne P McLaughlin, Philip J Stenger, et al.
Cancer Genetics and Cytogenetics|October 12, 2004
Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary siteStefan Meyer, Helen Kingston, A Malcolm R Taylor, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 13, 2012
Very mild presentation in adult with classical cellular phenotype of ataxia telangiectasiaPaul F Worth, Venkataramanan Srinivasan, Anna Smith, et al.
Pageof 24

Showing results (201-210 of 236) with videos related to

Sort By:
Pageof 24
Genomics|June 1, 1994
A physical map across chromosome 11q22-q23 containing the major locus for ataxia telangiectasiaH J Ambrose, P J Byrd, C M McConville, et al.
Analytical Chemistry|May 25, 2026
Nanopipettes Enable Native Mass Spectrometry Studies of the Intrinsically Disordered Protein α-Synuclein in Biochemical BuffersEmily J Byrd, Emma L Norgate, Joel A Crossley, et al.
Genomics|February 1, 1993
Irradiation hybrids for human chromosome 11: characterization and use for generating region-specific markers in 11q14-q23G T Gillett, C M McConville, P J Byrd, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 18, 2007
RIDDLE immunodeficiency syndrome is linked to defects in 53BP1-mediated DNA damage signalingGrant S Stewart, Tatjana Stankovic, Philip J Byrd, et al.
Cell|December 28, 1999
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorderG S Stewart, R S Maser, T Stankovic, et al.
Journal of Virology|December 17, 2010
Serotype-specific inactivation of the cellular DNA damage response during adenovirus infectionNatalie A Forrester, Garry G Sedgwick, Anoushka Thomas, et al.
Ophthalmology|September 1, 1991
Central photorefractive keratectomy for myopia. Partially sighted and normally sighted eyesM B McDonald, J C Liu, T J Byrd, et al.
Allergy and Asthma Proceedings|December 10, 2016
A comparison of seasonal trends in asthma exacerbations among children from geographic regions with different climatesJulia A Wisniewski, Anne P McLaughlin, Philip J Stenger, et al.
Cancer Genetics and Cytogenetics|October 12, 2004
Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary siteStefan Meyer, Helen Kingston, A Malcolm R Taylor, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 13, 2012
Very mild presentation in adult with classical cellular phenotype of ataxia telangiectasiaPaul F Worth, Venkataramanan Srinivasan, Anna Smith, et al.
Pageof 24