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Hatchell

Showing results (181-190 of 187) with videos related to

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Immunity|September 10, 2013
The pseudokinase MLKL mediates necroptosis via a molecular switch mechanismJames M Murphy, Peter E Czabotar, Joanne M Hildebrand, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2021
One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementationStephen E Lincoln, Tina Hambuch, Justin M Zook, et al.
BMC Medicine|August 18, 2021
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort studyEden V Haverfield, Edward D Esplin, Sienna J Aguilar, et al.
The Journal of Clinical Endocrinology and Metabolism|January 12, 2018
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D ConcentrationsJaeyoung Hong, Kathryn E Hatchell, Jonathan P Bradfield, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2023
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a changeHeidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, et al.
Nature Communications|June 21, 2020
A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunctionJoanne M Hildebrand, Maria Kauppi, Ian J Majewski, et al.
JAMA Neurology|October 31, 2022
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical PracticeDianalee McKnight, Ana Morales, Kathryn E Hatchell, et al.
Pageof 19

Showing results (181-190 of 187) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 187 results.
Immunity|September 10, 2013
The pseudokinase MLKL mediates necroptosis via a molecular switch mechanismJames M Murphy, Peter E Czabotar, Joanne M Hildebrand, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2021
One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementationStephen E Lincoln, Tina Hambuch, Justin M Zook, et al.
BMC Medicine|August 18, 2021
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort studyEden V Haverfield, Edward D Esplin, Sienna J Aguilar, et al.
The Journal of Clinical Endocrinology and Metabolism|January 12, 2018
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D ConcentrationsJaeyoung Hong, Kathryn E Hatchell, Jonathan P Bradfield, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2023
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a changeHeidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, et al.
Nature Communications|June 21, 2020
A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunctionJoanne M Hildebrand, Maria Kauppi, Ian J Majewski, et al.
JAMA Neurology|October 31, 2022
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical PracticeDianalee McKnight, Ana Morales, Kathryn E Hatchell, et al.
Pageof 19