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Nature Structural & Molecular Biology
|
September 5, 2017
N<sup>6</sup>-methyladenosine (m<sup>6</sup>A) recruits and repels proteins to regulate mRNA homeostasis
Raghu R Edupuganti, Simon Geiger, Rik G H Lindeboom, et al.
Biomolecules
|
June 24, 2022
Efficient Viral Transduction in Fetal and Adult Human Inner Ear Explants with AAV9-PHP.B Vectors
Edward S A van Beelen, Wouter H van der Valk, Thijs O Verhagen, et al.
European Journal of Medical Genetics
|
November 5, 2018
Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis
Laura V Vandervore, Rachel Schot, A Jeannette M Hoogeboom, et al.
American Journal of Physiology. Renal Physiology
|
February 27, 2025
Proteomic analysis of urinary extracellular vesicles from patients with ADTKD-HNF1β identifies roles for cilia-related proteins and serpins
Eveline J E M Kahlman, Martijn H van Heugten, Lotte E Tholen, et al.
Scientific Reports
|
June 16, 2016
Longitudinal monitoring of immunoglobulin A glycosylation during pregnancy by simultaneous MALDI-FTICR-MS analysis of N- and O-glycopeptides
Albert Bondt, Simone Nicolardi, Bas C Jansen, et al.
BMC Medical Genetics
|
April 17, 2009
The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients
Jean-Pierre Bayley, Anneliese E M Grimbergen, Patrick A van Bunderen, et al.
Nature Genetics
|
January 27, 2009
System-wide molecular evidence for phenotypic buffering in Arabidopsis
Jingyuan Fu, Joost J B Keurentjes, Harro Bouwmeester, et al.
BMC Bioinformatics
|
January 8, 2011
The MOLGENIS toolkit: rapid prototyping of biosoftware at the push of a button
Morris A Swertz, Martijn Dijkstra, Tomasz Adamusiak, et al.
Sleep Medicine
|
February 10, 2026
Circadian gene expression in adolescents: Associations with concurrent circadian disruption and subsequent changes in cardiometabolic risk measures
Donghan Su, Jaclyn M Goodrich, Jennifer T Lee, et al.
Orphanet Journal of Rare Diseases
|
February 9, 2019
The patient's view on rare disease trial design - a qualitative study
C M W Gaasterland, M C Jansen- van der Weide, M J du Prie-Olthof, et al.
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of 123
Search research articles
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Showing results (1071-1080 of 1,230) with videos related to
Sort By:
Page
of 123
Nature Structural & Molecular Biology
|
September 5, 2017
N<sup>6</sup>-methyladenosine (m<sup>6</sup>A) recruits and repels proteins to regulate mRNA homeostasis
Raghu R Edupuganti, Simon Geiger, Rik G H Lindeboom, et al.
Biomolecules
|
June 24, 2022
Efficient Viral Transduction in Fetal and Adult Human Inner Ear Explants with AAV9-PHP.B Vectors
Edward S A van Beelen, Wouter H van der Valk, Thijs O Verhagen, et al.
European Journal of Medical Genetics
|
November 5, 2018
Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis
Laura V Vandervore, Rachel Schot, A Jeannette M Hoogeboom, et al.
American Journal of Physiology. Renal Physiology
|
February 27, 2025
Proteomic analysis of urinary extracellular vesicles from patients with ADTKD-HNF1β identifies roles for cilia-related proteins and serpins
Eveline J E M Kahlman, Martijn H van Heugten, Lotte E Tholen, et al.
Scientific Reports
|
June 16, 2016
Longitudinal monitoring of immunoglobulin A glycosylation during pregnancy by simultaneous MALDI-FTICR-MS analysis of N- and O-glycopeptides
Albert Bondt, Simone Nicolardi, Bas C Jansen, et al.
BMC Medical Genetics
|
April 17, 2009
The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients
Jean-Pierre Bayley, Anneliese E M Grimbergen, Patrick A van Bunderen, et al.
Nature Genetics
|
January 27, 2009
System-wide molecular evidence for phenotypic buffering in Arabidopsis
Jingyuan Fu, Joost J B Keurentjes, Harro Bouwmeester, et al.
BMC Bioinformatics
|
January 8, 2011
The MOLGENIS toolkit: rapid prototyping of biosoftware at the push of a button
Morris A Swertz, Martijn Dijkstra, Tomasz Adamusiak, et al.
Sleep Medicine
|
February 10, 2026
Circadian gene expression in adolescents: Associations with concurrent circadian disruption and subsequent changes in cardiometabolic risk measures
Donghan Su, Jaclyn M Goodrich, Jennifer T Lee, et al.
Orphanet Journal of Rare Diseases
|
February 9, 2019
The patient's view on rare disease trial design - a qualitative study
C M W Gaasterland, M C Jansen- van der Weide, M J du Prie-Olthof, et al.
Page
of 123