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B Chadwick

Showing results (101-110 of 108) with videos related to

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American Journal of Human Genetics|February 17, 2001
Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomiaS A Slaugenhaupt, A Blumenfeld, S P Gill, et al.
Nature|February 29, 2000
Conversion of diploidy to haploidyH Yan, N Papadopoulos, G Marra, et al.
Cancer Research|March 14, 2001
MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancerJ Huang, S A Kuismanen, T Liu, et al.
Journal of Medical Genetics|January 17, 2014
A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndromeTaraneh Esmailpour, Hamidreza Riazifar, Linan Liu, et al.
Physical Review Letters|December 11, 2012
New precision measurements of the 235U(n,γ) cross sectionM Jandel, T A Bredeweg, E M Bond, et al.
European Journal of Dental Education : Official Journal of the Association for Dental Education in Europe|April 12, 2008
Evidence-based care and the curriculumT Winning, I Needleman, M Rohlin, et al.
Human Genetics|April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.
Neuromuscular Disorders : NMD|September 26, 2025
Consensus recommendations and considerations for the delivery and monitoring of gene therapy in patients with Duchenne muscular dystrophyJodi M Wolff, Nora Capocci, Evrim Atas, et al.
Pageof 11

Showing results (101-110 of 108) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 108 results.
American Journal of Human Genetics|February 17, 2001
Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomiaS A Slaugenhaupt, A Blumenfeld, S P Gill, et al.
Nature|February 29, 2000
Conversion of diploidy to haploidyH Yan, N Papadopoulos, G Marra, et al.
Cancer Research|March 14, 2001
MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancerJ Huang, S A Kuismanen, T Liu, et al.
Journal of Medical Genetics|January 17, 2014
A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndromeTaraneh Esmailpour, Hamidreza Riazifar, Linan Liu, et al.
Physical Review Letters|December 11, 2012
New precision measurements of the 235U(n,γ) cross sectionM Jandel, T A Bredeweg, E M Bond, et al.
European Journal of Dental Education : Official Journal of the Association for Dental Education in Europe|April 12, 2008
Evidence-based care and the curriculumT Winning, I Needleman, M Rohlin, et al.
Human Genetics|April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.
Neuromuscular Disorders : NMD|September 26, 2025
Consensus recommendations and considerations for the delivery and monitoring of gene therapy in patients with Duchenne muscular dystrophyJodi M Wolff, Nora Capocci, Evrim Atas, et al.
Pageof 11