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Showing results (651-660 of 687) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|December 14, 2011
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiencyNils Krone, Nicole Reisch, Jan Idkowiak, et al.
Nature Genetics|February 1, 2017
Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cystsEmma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
Nature Genetics|August 30, 2016
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cystsEmma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
American Journal of Human Genetics|June 5, 2018
De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental DisorderMargot R F Reijnders, Kerry A Miller, Mohsan Alvi, et al.
American Journal of Human Genetics|September 12, 2007
Clinical and molecular phenotype of Aicardi-Goutieres syndromeGillian Rice, Teresa Patrick, Rekha Parmar, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, 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.
Physical Review Letters|December 24, 2021
Point Absorber Limits to Future Gravitational-Wave DetectorsWenxuan Jia, Hiroaki Yamamoto, Kevin Kuns, et al.
Applied Optics|May 13, 2021
Point absorbers in Advanced LIGOAidan F Brooks, Gabriele Vajente, Hiro Yamamoto, et al.
Physical Review Letters|December 24, 2019
Quantum-Enhanced Advanced LIGO Detectors in the Era of Gravitational-Wave AstronomyM Tse, Haocun Yu, N Kijbunchoo, et al.
Pageof 69

Showing results (651-660 of 687) with videos related to

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Pageof 69
The Journal of Clinical Endocrinology and Metabolism|December 14, 2011
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiencyNils Krone, Nicole Reisch, Jan Idkowiak, et al.
Nature Genetics|February 1, 2017
Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cystsEmma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
Nature Genetics|August 30, 2016
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cystsEmma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
American Journal of Human Genetics|June 5, 2018
De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental DisorderMargot R F Reijnders, Kerry A Miller, Mohsan Alvi, et al.
American Journal of Human Genetics|September 12, 2007
Clinical and molecular phenotype of Aicardi-Goutieres syndromeGillian Rice, Teresa Patrick, Rekha Parmar, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, 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.
Physical Review Letters|December 24, 2021
Point Absorber Limits to Future Gravitational-Wave DetectorsWenxuan Jia, Hiroaki Yamamoto, Kevin Kuns, et al.
Applied Optics|May 13, 2021
Point absorbers in Advanced LIGOAidan F Brooks, Gabriele Vajente, Hiro Yamamoto, et al.
Physical Review Letters|December 24, 2019
Quantum-Enhanced Advanced LIGO Detectors in the Era of Gravitational-Wave AstronomyM Tse, Haocun Yu, N Kijbunchoo, et al.
Pageof 69