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Showing results (371-380 of 449) with videos related to

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Cerebral Cortex (New York, N.Y. : 1991)|September 12, 2014
Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral PhenotypePeter L Oliver, Rebecca A Chodroff, Amrit Gosal, et al.
American Journal of Human Genetics|October 10, 2001
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycanM Brockington, D J Blake, P Prandini, et al.
Regulatory Toxicology and Pharmacology : RTP|July 11, 2025
Evaluating the lifetime cumulative dose as a basis for carcinogenic potency of nitrosamines - a key tenet underpinning less-than-lifetime approaches for establishing acceptable intake limitsSusan P Felter, Ashley M Mudd, David J Ponting, et al.
Cell|September 4, 2010
The protein composition of mitotic chromosomes determined using multiclassifier combinatorial proteomicsShinya Ohta, Jimi-Carlo Bukowski-Wills, Luis Sanchez-Pulido, et al.
Human Molecular Genetics|January 4, 2001
The kyphoscoliosis (ky) mouse is deficient in hypertrophic responses and is caused by a mutation in a novel muscle-specific proteinG Blanco, G R Coulton, A Biggin, et al.
Elife|August 16, 2014
Considerations when investigating lncRNA function in vivoAndrew R Bassett, Asifa Akhtar, Denise P Barlow, et al.
Genome Research|November 5, 2014
Violation of the 12/23 rule of genomic V(D)J recombination is common in lymphocytesNicholas J Parkinson, Matthew Roddis, Ben Ferneyhough, et al.
Molecular Cell|July 15, 2009
Coordination of structure-specific nucleases by human SLX4/BTBD12 is required for DNA repairIvan M Muñoz, Karolina Hain, Anne-Cécile Déclais, et al.
European Urology|September 24, 2013
Next-generation sequencing of advanced prostate cancer treated with androgen-deprivation therapyPrabhakar Rajan, Ian M Sudbery, M Eugenia M Villasevil, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
The phenotypic spectrum of Xia-Gibbs syndromeYunyun Jiang, Michael F Wangler, Amy L McGuire, et al.
Pageof 45

Showing results (371-380 of 449) with videos related to

Sort By:
Pageof 45
Cerebral Cortex (New York, N.Y. : 1991)|September 12, 2014
Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral PhenotypePeter L Oliver, Rebecca A Chodroff, Amrit Gosal, et al.
American Journal of Human Genetics|October 10, 2001
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycanM Brockington, D J Blake, P Prandini, et al.
Regulatory Toxicology and Pharmacology : RTP|July 11, 2025
Evaluating the lifetime cumulative dose as a basis for carcinogenic potency of nitrosamines - a key tenet underpinning less-than-lifetime approaches for establishing acceptable intake limitsSusan P Felter, Ashley M Mudd, David J Ponting, et al.
Cell|September 4, 2010
The protein composition of mitotic chromosomes determined using multiclassifier combinatorial proteomicsShinya Ohta, Jimi-Carlo Bukowski-Wills, Luis Sanchez-Pulido, et al.
Human Molecular Genetics|January 4, 2001
The kyphoscoliosis (ky) mouse is deficient in hypertrophic responses and is caused by a mutation in a novel muscle-specific proteinG Blanco, G R Coulton, A Biggin, et al.
Elife|August 16, 2014
Considerations when investigating lncRNA function in vivoAndrew R Bassett, Asifa Akhtar, Denise P Barlow, et al.
Genome Research|November 5, 2014
Violation of the 12/23 rule of genomic V(D)J recombination is common in lymphocytesNicholas J Parkinson, Matthew Roddis, Ben Ferneyhough, et al.
Molecular Cell|July 15, 2009
Coordination of structure-specific nucleases by human SLX4/BTBD12 is required for DNA repairIvan M Muñoz, Karolina Hain, Anne-Cécile Déclais, et al.
European Urology|September 24, 2013
Next-generation sequencing of advanced prostate cancer treated with androgen-deprivation therapyPrabhakar Rajan, Ian M Sudbery, M Eugenia M Villasevil, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
The phenotypic spectrum of Xia-Gibbs syndromeYunyun Jiang, Michael F Wangler, Amy L McGuire, et al.
Pageof 45