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A Curtin

Showing results (161-170 of 189) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|July 23, 2024
International Society on Thrombosis and Haemostasis clinical practice guideline for treatment of congenital hemophilia A and B based on the Grading of Recommendations Assessment, Development, and Evaluation methodologySuely M Rezende, Ignacio Neumann, Pantep Angchaisuksiri, et al.
The British Journal of Nutrition|August 23, 2018
Vitamin D receptor genotype influences risk of upper respiratory infectionDavid A Jolliffe, Claire L Greiller, Charles A Mein, et al.
Blood Advances|April 27, 2022
Functional interaction between compound heterozygous TERT mutations causes severe telomere biology disorderAram Niaz, Jia Truong, Annabel Manoleras, et al.
Current Biology : CB|July 5, 2003
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, et al.
Nature|January 25, 2018
Biomechanics of predator-prey arms race in lion, zebra, cheetah and impalaAlan M Wilson, Tatjana Y Hubel, Simon D Wilshin, et al.
Pediatric Pulmonology|March 31, 2019
Nocturnal asthma is affected by genetic interactions between RORA and NPSR1Vincent D Gaertner, Sven Michel, John A Curtin, et al.
Ejhaem|July 18, 2022
A novel cause of <i>DKC1</i>-related bone marrow failure: Partial deletion of the 3' untranslated regionJonathan W Arthur, Hilda A Pickett, Pasquale M Barbaro, et al.
The Medical Journal of Australia|May 4, 2005
Treatment of an infant with X-linked severe combined immunodeficiency (SCID-X1) by gene therapy in AustraliaSamantha L Ginn, Julie A Curtin, Belinda Kramer, et al.
Comparative and Functional Genomics|July 17, 2008
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouseVicky Tsipouri, John A Curtin, Pat M Nolan, et al.
The Journal of Allergy and Clinical Immunology|December 25, 2016
Epigenome-wide analysis links SMAD3 methylation at birth to asthma in children of asthmatic mothersAvery DeVries, Gabriela Wlasiuk, Susan J Miller, et al.
Pageof 19

Showing results (161-170 of 189) with videos related to

Sort By:
Pageof 19
Journal of Thrombosis and Haemostasis : JTH|July 23, 2024
International Society on Thrombosis and Haemostasis clinical practice guideline for treatment of congenital hemophilia A and B based on the Grading of Recommendations Assessment, Development, and Evaluation methodologySuely M Rezende, Ignacio Neumann, Pantep Angchaisuksiri, et al.
The British Journal of Nutrition|August 23, 2018
Vitamin D receptor genotype influences risk of upper respiratory infectionDavid A Jolliffe, Claire L Greiller, Charles A Mein, et al.
Blood Advances|April 27, 2022
Functional interaction between compound heterozygous TERT mutations causes severe telomere biology disorderAram Niaz, Jia Truong, Annabel Manoleras, et al.
Current Biology : CB|July 5, 2003
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, et al.
Nature|January 25, 2018
Biomechanics of predator-prey arms race in lion, zebra, cheetah and impalaAlan M Wilson, Tatjana Y Hubel, Simon D Wilshin, et al.
Pediatric Pulmonology|March 31, 2019
Nocturnal asthma is affected by genetic interactions between RORA and NPSR1Vincent D Gaertner, Sven Michel, John A Curtin, et al.
Ejhaem|July 18, 2022
A novel cause of <i>DKC1</i>-related bone marrow failure: Partial deletion of the 3' untranslated regionJonathan W Arthur, Hilda A Pickett, Pasquale M Barbaro, et al.
The Medical Journal of Australia|May 4, 2005
Treatment of an infant with X-linked severe combined immunodeficiency (SCID-X1) by gene therapy in AustraliaSamantha L Ginn, Julie A Curtin, Belinda Kramer, et al.
Comparative and Functional Genomics|July 17, 2008
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouseVicky Tsipouri, John A Curtin, Pat M Nolan, et al.
The Journal of Allergy and Clinical Immunology|December 25, 2016
Epigenome-wide analysis links SMAD3 methylation at birth to asthma in children of asthmatic mothersAvery DeVries, Gabriela Wlasiuk, Susan J Miller, et al.
Pageof 19