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B Dobbs

Showing results (171-180 of 218) with videos related to

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Journal of Medical Genetics|April 25, 2024
Exome sequencing of 1190 non-syndromic clubfoot cases reveals <i>HOXD12</i> as a novel disease geneWu-Lin Charng, Momchil Nikolov, Isabel Shrestha, et al.
Pediatric Neurology|March 2, 2020
Prevalence and Impact of Underlying Diagnosis and Comorbidities on Chiari 1 MalformationBrooke Sadler, Timothy Kuensting, Jennifer Strahle, et al.
Cellular Reprogramming|August 10, 2010
Porcine skin-derived progenitor (SKP) spheres and neurospheres: Distinct "stemness" identified by microarray analysisMing-Tao Zhao, Kristin M Whitworth, Hui Lin, et al.
Clinical Orthopaedics and Related Research|November 27, 2013
Fairness to all: gender and sex in scientific reportingSeth S Leopold, Lee Beadling, Matthew B Dobbs, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 27, 2014
The WNT signaling antagonist Dickkopf-1 directs lineage commitment and promotes survival of the preimplantation embryoAnna C Denicol, Jeremy Block, Dale E Kelley, et al.
Spine|January 14, 2009
Genetic linkage localizes an adolescent idiopathic scoliosis and pectus excavatum gene to chromosome 18 qChristina A Gurnett, Farhang Alaee, Anne Bowcock, et al.
Clinical Orthopaedics and Related Research|July 1, 2017
Editorial: How Does CORR <sup>®</sup> Evaluate Survey Studies?Matthew B Dobbs, Mark C Gebhardt, Terence J Gioe, et al.
Clinical Orthopaedics and Related Research|February 12, 2015
Editorial: Estimating survivorship in the face of competing risksM Daniel Wongworawat, Matthew B Dobbs, Mark C Gebhardt, et al.
Biology of Reproduction|January 23, 2015
Impairment of preimplantation porcine embryo development by histone demethylase KDM5B knockdown through disturbance of bivalent H3K4me3-H3K27me3 modificationsJiaojiao Huang, Hongyong Zhang, Xianlong Wang, et al.
BMC Medical Genetics|July 12, 2011
Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotypeTracy L McGregor, Christina A Gurnett, Matthew B Dobbs, et al.
Pageof 22

Showing results (171-180 of 218) with videos related to

Sort By:
Pageof 22
Journal of Medical Genetics|April 25, 2024
Exome sequencing of 1190 non-syndromic clubfoot cases reveals <i>HOXD12</i> as a novel disease geneWu-Lin Charng, Momchil Nikolov, Isabel Shrestha, et al.
Pediatric Neurology|March 2, 2020
Prevalence and Impact of Underlying Diagnosis and Comorbidities on Chiari 1 MalformationBrooke Sadler, Timothy Kuensting, Jennifer Strahle, et al.
Cellular Reprogramming|August 10, 2010
Porcine skin-derived progenitor (SKP) spheres and neurospheres: Distinct "stemness" identified by microarray analysisMing-Tao Zhao, Kristin M Whitworth, Hui Lin, et al.
Clinical Orthopaedics and Related Research|November 27, 2013
Fairness to all: gender and sex in scientific reportingSeth S Leopold, Lee Beadling, Matthew B Dobbs, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 27, 2014
The WNT signaling antagonist Dickkopf-1 directs lineage commitment and promotes survival of the preimplantation embryoAnna C Denicol, Jeremy Block, Dale E Kelley, et al.
Spine|January 14, 2009
Genetic linkage localizes an adolescent idiopathic scoliosis and pectus excavatum gene to chromosome 18 qChristina A Gurnett, Farhang Alaee, Anne Bowcock, et al.
Clinical Orthopaedics and Related Research|July 1, 2017
Editorial: How Does CORR <sup>®</sup> Evaluate Survey Studies?Matthew B Dobbs, Mark C Gebhardt, Terence J Gioe, et al.
Clinical Orthopaedics and Related Research|February 12, 2015
Editorial: Estimating survivorship in the face of competing risksM Daniel Wongworawat, Matthew B Dobbs, Mark C Gebhardt, et al.
Biology of Reproduction|January 23, 2015
Impairment of preimplantation porcine embryo development by histone demethylase KDM5B knockdown through disturbance of bivalent H3K4me3-H3K27me3 modificationsJiaojiao Huang, Hongyong Zhang, Xianlong Wang, et al.
BMC Medical Genetics|July 12, 2011
Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotypeTracy L McGregor, Christina A Gurnett, Matthew B Dobbs, et al.
Pageof 22