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DINGER

Showing results (541-550 of 603) with videos related to

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Cell Reports|October 26, 2017
A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic EncephalopathySushmitha Gururaj, Elizabeth Emma Palmer, Garrett D Sheehan, et al.
Genome Research|June 20, 2008
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiationMarcel E Dinger, Paulo P Amaral, Tim R Mercer, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 27, 1999
Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindredA T Remaley, S Rust, M Rosier, et al.
The EMBO Journal|August 29, 2024
Human genomic DNA is widely interspersed with i-motif structuresCristian David Peña Martinez, Mahdi Zeraati, Romain Rouet, et al.
Neuroradiology|February 3, 2026
Ultra-low dose protocol on photon-counting computed tomography as an alternative to radiographic shunt series in the diagnosis of mechanical ventriculoperitoneal shunt complications - an ex vivo phantom study for children and adultsBerk Yildirim, Aydin Demircioğlu, Raya Ocker-Serger, et al.
RNA (New York, N.Y.)|April 5, 2011
SNORD-host RNA Zfas1 is a regulator of mammary development and a potential marker for breast cancerMarjan E Askarian-Amiri, Joanna Crawford, Juliet D French, et al.
Journal of the National Cancer Institute|June 8, 2014
Effects of a novel long noncoding RNA, lncUSMycN, on N-Myc expression and neuroblastoma progressionPei Y Liu, Daniela Erriquez, Glenn M Marshall, et al.
European Journal of Human Genetics : EJHG|January 13, 2021
Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencingAmali C Mallawaarachchi, Ben Lundie, Yvonne Hort, et al.
Journal of Medical Genetics|May 27, 2019
Pathogenic variants in <i>PLOD3</i> result in a Stickler syndrome-like connective tissue disorder with vascular complicationsLisa Jean Ewans, Alison Colley, Carles Gaston-Massuet, et al.
The Journal of Experimental Medicine|July 9, 2020
Mutations in the exocyst component EXOC2 cause severe defects in human brain developmentNicole J Van Bergen, Syed Mukhtar Ahmed, Felicity Collins, et al.
Pageof 61

Showing results (541-550 of 603) with videos related to

Sort By:
Pageof 61
Cell Reports|October 26, 2017
A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic EncephalopathySushmitha Gururaj, Elizabeth Emma Palmer, Garrett D Sheehan, et al.
Genome Research|June 20, 2008
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiationMarcel E Dinger, Paulo P Amaral, Tim R Mercer, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 27, 1999
Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindredA T Remaley, S Rust, M Rosier, et al.
The EMBO Journal|August 29, 2024
Human genomic DNA is widely interspersed with i-motif structuresCristian David Peña Martinez, Mahdi Zeraati, Romain Rouet, et al.
Neuroradiology|February 3, 2026
Ultra-low dose protocol on photon-counting computed tomography as an alternative to radiographic shunt series in the diagnosis of mechanical ventriculoperitoneal shunt complications - an ex vivo phantom study for children and adultsBerk Yildirim, Aydin Demircioğlu, Raya Ocker-Serger, et al.
RNA (New York, N.Y.)|April 5, 2011
SNORD-host RNA Zfas1 is a regulator of mammary development and a potential marker for breast cancerMarjan E Askarian-Amiri, Joanna Crawford, Juliet D French, et al.
Journal of the National Cancer Institute|June 8, 2014
Effects of a novel long noncoding RNA, lncUSMycN, on N-Myc expression and neuroblastoma progressionPei Y Liu, Daniela Erriquez, Glenn M Marshall, et al.
European Journal of Human Genetics : EJHG|January 13, 2021
Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencingAmali C Mallawaarachchi, Ben Lundie, Yvonne Hort, et al.
Journal of Medical Genetics|May 27, 2019
Pathogenic variants in <i>PLOD3</i> result in a Stickler syndrome-like connective tissue disorder with vascular complicationsLisa Jean Ewans, Alison Colley, Carles Gaston-Massuet, et al.
The Journal of Experimental Medicine|July 9, 2020
Mutations in the exocyst component EXOC2 cause severe defects in human brain developmentNicole J Van Bergen, Syed Mukhtar Ahmed, Felicity Collins, et al.
Pageof 61