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Showing results (91-100 of 111) with videos related to

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Ultrasound International Open|June 9, 2021
Gastrointestinal Ultrasound in Functional Disorders of the Gastrointestinal Tract - EFSUMB Consensus StatementGiovanni Maconi, Trygve Hausken, Christoph F Dietrich, et al.
Journal of Medical Genetics|May 3, 2005
A new syndrome, congenital extraocular muscle fibrosis with ulnar hand anomalies, maps to chromosome 21qterT Tukel, A Uzumcu, A Gezer, et al.
Journal of Medicinal Chemistry|May 14, 1993
2'-substituted chalcone derivatives as inhibitors of interleukin-1 biosynthesisD G Batt, R Goodman, D G Jones, et al.
Journal of Enzyme Inhibition|January 1, 1996
Comparative effects of selective cyclooxygenase 1 and cyclooxygenase 2 inhibitors on myeloperoxidase and 3 alpha-hydroxysteroid dehydrogenaseN L Rider, D Pinto, M Covington, et al.
American Journal of Human Genetics|August 28, 2018
Genetic Regulatory Mechanisms of Smooth Muscle Cells Map to Coronary Artery Disease Risk LociBoxiang Liu, Milos Pjanic, Ting Wang, et al.
Journal of the American Society of Nephrology : JASN|May 23, 2003
A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2Rainer G Ruf, Matthias T F Wolf, Hans C Hennies, et al.
Neurology|January 12, 2005
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizuresR Straussberg, L Basel-Vanagaite, S Kivity, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 20, 2013
Genome-wide protein QTL mapping identifies human plasma kallikrein as a post-translational regulator of serum uPAR levelsMichael A Portelli, Mateusz Siedlinski, Ceri E Stewart, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 3, 2005
Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkageMatthias T F Wolf, Isabella Zalewski, Félix Claverie Martin, et al.
Journal of Genetics|August 13, 2025
Genetic analysis in a consanguineous MCPH family revealed a refinement of the MCPH12 locus and a founder effect of the recurrent <i>CDK6</i> variant [c.589G>A, p.(Ala197Thr)] in the Pakistani populationMuzammil Ahmad Khan, Jasmin Blatterer, Markus Kuster, et al.
Pageof 12

Showing results (91-100 of 111) with videos related to

Sort By:
Pageof 12
Ultrasound International Open|June 9, 2021
Gastrointestinal Ultrasound in Functional Disorders of the Gastrointestinal Tract - EFSUMB Consensus StatementGiovanni Maconi, Trygve Hausken, Christoph F Dietrich, et al.
Journal of Medical Genetics|May 3, 2005
A new syndrome, congenital extraocular muscle fibrosis with ulnar hand anomalies, maps to chromosome 21qterT Tukel, A Uzumcu, A Gezer, et al.
Journal of Medicinal Chemistry|May 14, 1993
2'-substituted chalcone derivatives as inhibitors of interleukin-1 biosynthesisD G Batt, R Goodman, D G Jones, et al.
Journal of Enzyme Inhibition|January 1, 1996
Comparative effects of selective cyclooxygenase 1 and cyclooxygenase 2 inhibitors on myeloperoxidase and 3 alpha-hydroxysteroid dehydrogenaseN L Rider, D Pinto, M Covington, et al.
American Journal of Human Genetics|August 28, 2018
Genetic Regulatory Mechanisms of Smooth Muscle Cells Map to Coronary Artery Disease Risk LociBoxiang Liu, Milos Pjanic, Ting Wang, et al.
Journal of the American Society of Nephrology : JASN|May 23, 2003
A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2Rainer G Ruf, Matthias T F Wolf, Hans C Hennies, et al.
Neurology|January 12, 2005
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizuresR Straussberg, L Basel-Vanagaite, S Kivity, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 20, 2013
Genome-wide protein QTL mapping identifies human plasma kallikrein as a post-translational regulator of serum uPAR levelsMichael A Portelli, Mateusz Siedlinski, Ceri E Stewart, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 3, 2005
Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkageMatthias T F Wolf, Isabella Zalewski, Félix Claverie Martin, et al.
Journal of Genetics|August 13, 2025
Genetic analysis in a consanguineous MCPH family revealed a refinement of the MCPH12 locus and a founder effect of the recurrent <i>CDK6</i> variant [c.589G>A, p.(Ala197Thr)] in the Pakistani populationMuzammil Ahmad Khan, Jasmin Blatterer, Markus Kuster, et al.
Pageof 12