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Stephen F Kingsmore

Showing results (51-60 of 171) with videos related to

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The Journal of Infectious Diseases|July 18, 2006
Cytokine expression patterns associated with systemic adverse events following smallpox immunizationBrett A McKinney, David M Reif, Michael T Rock, et al.
Cold Spring Harbor Molecular Case Studies|June 12, 2021
Postmortem whole-genome sequencing on a dried blood spot identifies a novel homozygous SUOX variant causing isolated sulfite oxidase deficiencyMallory J Owen, Jerica Lenberg, Annette Feigenbaum, et al.
International Journal of Neonatal Screening|November 21, 2023
NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening StakeholdersKee Chan, Zhanzhi Hu, Lynn W Bush, et al.
Nature|November 4, 2008
Alternative isoform regulation in human tissue transcriptomesEric T Wang, Rickard Sandberg, Shujun Luo, et al.
Clinical Therapeutics|July 10, 2023
Assessing Diversity in Newborn Genomic Sequencing Research Recruitment: Race/Ethnicity and Primary Spoken Language Variation in Eligibility, Enrollment, and Reasons for DecliningJulie A Cakici, David Dimmock, Sara Caylor, et al.
Critical Care (London, England)|April 19, 2015
Human metabolic response to systemic inflammation: assessment of the concordance between experimental endotoxemia and clinical cases of sepsis/SIRSKubra Kamisoglu, Beatrice Haimovich, Steve E Calvano, et al.
NPJ Genomic Medicine|August 22, 2020
Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnosesKiely N James, Michelle M Clark, Brandon Camp, et al.
Human Molecular Genetics|March 26, 2002
The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle traffickingQing Zhang, Wei Li, Edward K Novak, et al.
Cold Spring Harbor Molecular Case Studies|February 5, 2020
Mortality in a neonate with molybdenum cofactor deficiency illustrates the need for a comprehensive rapid precision medicine systemStephen F Kingsmore, Nanda Ramchandar, Kiely James, et al.
Genome Research|April 16, 2003
Unbiased whole-genome amplification directly from clinical samplesSeiyu Hosono, A Fawad Faruqi, Frank B Dean, et al.
Pageof 18

Showing results (51-60 of 171) with videos related to

Sort By:
Pageof 18
The Journal of Infectious Diseases|July 18, 2006
Cytokine expression patterns associated with systemic adverse events following smallpox immunizationBrett A McKinney, David M Reif, Michael T Rock, et al.
Cold Spring Harbor Molecular Case Studies|June 12, 2021
Postmortem whole-genome sequencing on a dried blood spot identifies a novel homozygous SUOX variant causing isolated sulfite oxidase deficiencyMallory J Owen, Jerica Lenberg, Annette Feigenbaum, et al.
International Journal of Neonatal Screening|November 21, 2023
NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening StakeholdersKee Chan, Zhanzhi Hu, Lynn W Bush, et al.
Nature|November 4, 2008
Alternative isoform regulation in human tissue transcriptomesEric T Wang, Rickard Sandberg, Shujun Luo, et al.
Clinical Therapeutics|July 10, 2023
Assessing Diversity in Newborn Genomic Sequencing Research Recruitment: Race/Ethnicity and Primary Spoken Language Variation in Eligibility, Enrollment, and Reasons for DecliningJulie A Cakici, David Dimmock, Sara Caylor, et al.
Critical Care (London, England)|April 19, 2015
Human metabolic response to systemic inflammation: assessment of the concordance between experimental endotoxemia and clinical cases of sepsis/SIRSKubra Kamisoglu, Beatrice Haimovich, Steve E Calvano, et al.
NPJ Genomic Medicine|August 22, 2020
Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnosesKiely N James, Michelle M Clark, Brandon Camp, et al.
Human Molecular Genetics|March 26, 2002
The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle traffickingQing Zhang, Wei Li, Edward K Novak, et al.
Cold Spring Harbor Molecular Case Studies|February 5, 2020
Mortality in a neonate with molybdenum cofactor deficiency illustrates the need for a comprehensive rapid precision medicine systemStephen F Kingsmore, Nanda Ramchandar, Kiely James, et al.
Genome Research|April 16, 2003
Unbiased whole-genome amplification directly from clinical samplesSeiyu Hosono, A Fawad Faruqi, Frank B Dean, et al.
Pageof 18