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Daniel Nilsson

Showing results (131-140 of 178) with videos related to

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Frontiers in Immunology|January 25, 2014
An N-Terminal Missense Mutation in STX11 Causative of FHL4 Abrogates Syntaxin-11 Binding to Munc18-2Martha-Lena Müller, Samuel C C Chiang, Marie Meeths, et al.
Bioinformatics (Oxford, England)|February 19, 2026
Nallo: a Nextflow pipeline for comprehensive human long-read genome analysisFelix Lenner, Anders Jemt, Lucia Peña Pérez, et al.
Optics Letters|December 22, 2012
Ronchi test for characterization of nanofocusing optics at a hard x-ray free-electron laserDaniel Nilsson, Fredrik Uhlén, Anders Holmberg, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 14, 2017
A Large Inversion Involving GNAS Exon A/B and All Exons Encoding Gsα Is Associated With Autosomal Dominant Pseudohypoparathyroidism Type Ib (PHP1B)Giedre Grigelioniene, Pasi I Nevalainen, Monica Reyes, et al.
Journal of Medical Genetics|May 3, 2013
A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGTMalin Kvarnung, Daniel Nilsson, Anna Lindstrand, et al.
Human Mutation|August 7, 2018
Alu-Alu mediated intragenic duplications in IFT81 and MATN3 are associated with skeletal dysplasiasMaria Pettersson, Raquel Vaz, Anna Hammarsjö, et al.
Human Molecular Genetics|June 25, 2015
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafishIzabella Baranowska Körberg, Wolfgang Hofmeister, Ellen Markljung, et al.
Diabetes|May 28, 2005
Adipocyte-specific overexpression of FOXC2 prevents diet-induced increases in intramuscular fatty acyl CoA and insulin resistanceJason K Kim, Hyo-Jeong Kim, So-Young Park, et al.
Journal of Medical Genetics|December 5, 2014
CTNND2-a candidate gene for reading problems and mild intellectual disabilityWolfgang Hofmeister, Daniel Nilsson, Alexandra Topa, et al.
Pediatric Blood & Cancer|April 20, 2017
Hepatic sinusoidal obstruction syndrome during maintenance therapy of childhood acute lymphoblastic leukemia is associated with continuous asparaginase therapy and mercaptopurine metabolitesLinea Natalie Toksvang, Silvia De Pietri, Stine N Nielsen, et al.
Pageof 18

Showing results (131-140 of 178) with videos related to

Sort By:
Pageof 18
Frontiers in Immunology|January 25, 2014
An N-Terminal Missense Mutation in STX11 Causative of FHL4 Abrogates Syntaxin-11 Binding to Munc18-2Martha-Lena Müller, Samuel C C Chiang, Marie Meeths, et al.
Bioinformatics (Oxford, England)|February 19, 2026
Nallo: a Nextflow pipeline for comprehensive human long-read genome analysisFelix Lenner, Anders Jemt, Lucia Peña Pérez, et al.
Optics Letters|December 22, 2012
Ronchi test for characterization of nanofocusing optics at a hard x-ray free-electron laserDaniel Nilsson, Fredrik Uhlén, Anders Holmberg, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 14, 2017
A Large Inversion Involving GNAS Exon A/B and All Exons Encoding Gsα Is Associated With Autosomal Dominant Pseudohypoparathyroidism Type Ib (PHP1B)Giedre Grigelioniene, Pasi I Nevalainen, Monica Reyes, et al.
Journal of Medical Genetics|May 3, 2013
A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGTMalin Kvarnung, Daniel Nilsson, Anna Lindstrand, et al.
Human Mutation|August 7, 2018
Alu-Alu mediated intragenic duplications in IFT81 and MATN3 are associated with skeletal dysplasiasMaria Pettersson, Raquel Vaz, Anna Hammarsjö, et al.
Human Molecular Genetics|June 25, 2015
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafishIzabella Baranowska Körberg, Wolfgang Hofmeister, Ellen Markljung, et al.
Diabetes|May 28, 2005
Adipocyte-specific overexpression of FOXC2 prevents diet-induced increases in intramuscular fatty acyl CoA and insulin resistanceJason K Kim, Hyo-Jeong Kim, So-Young Park, et al.
Journal of Medical Genetics|December 5, 2014
CTNND2-a candidate gene for reading problems and mild intellectual disabilityWolfgang Hofmeister, Daniel Nilsson, Alexandra Topa, et al.
Pediatric Blood & Cancer|April 20, 2017
Hepatic sinusoidal obstruction syndrome during maintenance therapy of childhood acute lymphoblastic leukemia is associated with continuous asparaginase therapy and mercaptopurine metabolitesLinea Natalie Toksvang, Silvia De Pietri, Stine N Nielsen, et al.
Pageof 18