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C Cox

Showing results (1391-1400 of 1,430) with videos related to

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American Journal of Human Genetics|May 8, 2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndromeMark J Rieder, Glenn E Green, Sarah S Park, et al.
Plos Genetics|September 21, 2011
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and miceLisenka E L M Vissers, Timothy C Cox, A Murat Maga, et al.
Sleep Health|September 30, 2023
Distribution of dim light melatonin offset (DLMOff) and phase relationship to waketime in healthy adults and associations with chronotypeRebecca C Cox, Alivia B Blumenstein, Tina M Burke, et al.
Journal of Clinical Medicine|August 7, 2021
Chronic Critical Illness Elicits a Unique Circulating Leukocyte Transcriptome in Sepsis SurvivorsDijoia B Darden, Gabriela L Ghita, Zhongkai Wang, et al.
Frontiers in Immunology|July 17, 2020
Identification of Unique mRNA and miRNA Expression Patterns in Bone Marrow Hematopoietic Stem and Progenitor Cells After Trauma in Older AdultsDijoia B Darden, Julie A Stortz, McKenzie K Hollen, et al.
Journal of Medical Genetics|April 22, 2011
Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1Anne M Slavotinek, Sergio E Baranzini, Denny Schanze, et al.
Clinical Journal of the American Society of Nephrology : CJASN|February 14, 2023
Team-Based Coaching Intervention to Improve Contrast-Associated Acute Kidney Injury: A Cluster-Randomized TrialJeremiah R Brown, Richard Solomon, Meagan E Stabler, et al.
Leukemia|June 22, 2001
The prognostic value of cytogenetics is reinforced by the kind of induction/consolidation therapy in influencing the outcome of acute myeloid leukemia--analysis of 848 patientsG Visani, P Bernasconi, M Boni, et al.
Critical Care (London, England)|November 15, 2019
Myeloid-derived suppressor cell function and epigenetic expression evolves over time after surgical sepsisMcKenzie K Hollen, Julie A Stortz, Dijoia Darden, et al.
Genome Research|April 15, 2025
Common <i>cis</i>-regulatory variation modifies the penetrance of pathogenic <i>SHROOM3</i> variants in craniofacial microsomiaHao Zhu, Jiao Zhang, Soumya Rao, et al.
Pageof 143

Showing results (1391-1400 of 1,430) with videos related to

Sort By:
Pageof 143
American Journal of Human Genetics|May 8, 2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndromeMark J Rieder, Glenn E Green, Sarah S Park, et al.
Plos Genetics|September 21, 2011
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and miceLisenka E L M Vissers, Timothy C Cox, A Murat Maga, et al.
Sleep Health|September 30, 2023
Distribution of dim light melatonin offset (DLMOff) and phase relationship to waketime in healthy adults and associations with chronotypeRebecca C Cox, Alivia B Blumenstein, Tina M Burke, et al.
Journal of Clinical Medicine|August 7, 2021
Chronic Critical Illness Elicits a Unique Circulating Leukocyte Transcriptome in Sepsis SurvivorsDijoia B Darden, Gabriela L Ghita, Zhongkai Wang, et al.
Frontiers in Immunology|July 17, 2020
Identification of Unique mRNA and miRNA Expression Patterns in Bone Marrow Hematopoietic Stem and Progenitor Cells After Trauma in Older AdultsDijoia B Darden, Julie A Stortz, McKenzie K Hollen, et al.
Journal of Medical Genetics|April 22, 2011
Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1Anne M Slavotinek, Sergio E Baranzini, Denny Schanze, et al.
Clinical Journal of the American Society of Nephrology : CJASN|February 14, 2023
Team-Based Coaching Intervention to Improve Contrast-Associated Acute Kidney Injury: A Cluster-Randomized TrialJeremiah R Brown, Richard Solomon, Meagan E Stabler, et al.
Leukemia|June 22, 2001
The prognostic value of cytogenetics is reinforced by the kind of induction/consolidation therapy in influencing the outcome of acute myeloid leukemia--analysis of 848 patientsG Visani, P Bernasconi, M Boni, et al.
Critical Care (London, England)|November 15, 2019
Myeloid-derived suppressor cell function and epigenetic expression evolves over time after surgical sepsisMcKenzie K Hollen, Julie A Stortz, Dijoia Darden, et al.
Genome Research|April 15, 2025
Common <i>cis</i>-regulatory variation modifies the penetrance of pathogenic <i>SHROOM3</i> variants in craniofacial microsomiaHao Zhu, Jiao Zhang, Soumya Rao, et al.
Pageof 143