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Showing results (631-640 of 649) with videos related to

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Nature Genetics|August 1, 1996
Plectin deficiency results in muscular dystrophy with epidermolysis bullosaF J Smith, R A Eady, I M Leigh, et al.
The British Journal of Dermatology|March 25, 2011
Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populationsH Chen, J E A Common, R L Haines, et al.
Critical Care Medicine|February 8, 2021
Choosing Wisely For Critical Care: The Next FiveJerry J Zimmerman, Lori A Harmon, Pamela L Smithburger, et al.
American Journal of Human Genetics|December 15, 2000
BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertensionR D Machado, M W Pauciulo, J R Thomson, et al.
Journal of Neurodevelopmental Disorders|May 15, 2022
Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history studyCaroline B Buchanan, Jennifer L Stallworth, Aubin E Joy, et al.
Pediatric Neurology|August 13, 2021
Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental SyndromesOlivia J Veatch, Beth A Malow, Hye-Seung Lee, et al.
Critical Care Medicine|June 21, 2023
The Reviewer Academy of the Society of Critical Care Medicine: Key Principles and Strategic PlanPeta M A Alexander, Rebecca A Aslakson, Erin F Barreto, et al.
American Journal of Respiratory and Critical Care Medicine|March 13, 2024
Tackling Brain and Muscle Dysfunction in Acute Respiratory Distress Syndrome Survivors: NHLBI Workshop ReportJessica A Palakshappa, Jane A E Batt, Sue C Bodine, et al.
Applied Optics|May 13, 2021
Point absorbers in Advanced LIGOAidan F Brooks, Gabriele Vajente, Hiro Yamamoto, et al.
Science (New York, N.Y.)|June 18, 2021
Approaching the motional ground state of a 10-kg objectChris Whittle, Evan D Hall, Sheila Dwyer, et al.
Pageof 65

Showing results (631-640 of 649) with videos related to

Sort By:
Pageof 65
Nature Genetics|August 1, 1996
Plectin deficiency results in muscular dystrophy with epidermolysis bullosaF J Smith, R A Eady, I M Leigh, et al.
The British Journal of Dermatology|March 25, 2011
Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populationsH Chen, J E A Common, R L Haines, et al.
Critical Care Medicine|February 8, 2021
Choosing Wisely For Critical Care: The Next FiveJerry J Zimmerman, Lori A Harmon, Pamela L Smithburger, et al.
American Journal of Human Genetics|December 15, 2000
BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertensionR D Machado, M W Pauciulo, J R Thomson, et al.
Journal of Neurodevelopmental Disorders|May 15, 2022
Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history studyCaroline B Buchanan, Jennifer L Stallworth, Aubin E Joy, et al.
Pediatric Neurology|August 13, 2021
Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental SyndromesOlivia J Veatch, Beth A Malow, Hye-Seung Lee, et al.
Critical Care Medicine|June 21, 2023
The Reviewer Academy of the Society of Critical Care Medicine: Key Principles and Strategic PlanPeta M A Alexander, Rebecca A Aslakson, Erin F Barreto, et al.
American Journal of Respiratory and Critical Care Medicine|March 13, 2024
Tackling Brain and Muscle Dysfunction in Acute Respiratory Distress Syndrome Survivors: NHLBI Workshop ReportJessica A Palakshappa, Jane A E Batt, Sue C Bodine, et al.
Applied Optics|May 13, 2021
Point absorbers in Advanced LIGOAidan F Brooks, Gabriele Vajente, Hiro Yamamoto, et al.
Science (New York, N.Y.)|June 18, 2021
Approaching the motional ground state of a 10-kg objectChris Whittle, Evan D Hall, Sheila Dwyer, et al.
Pageof 65