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The Plant Cell
|
February 22, 2019
Regulation of Oxygenic Photosynthesis during Trophic Transitions in the Green Alga <i>Chromochloris zofingiensis</i>
Melissa S Roth, Sean D Gallaher, Daniel J Westcott, et al.
Scientific Reports
|
November 27, 2025
Demonstrating soft X-ray tomography in the lab for correlative cryogenic biological imaging using X-rays and light microscopy
Stephen O'Connor, David Rogers, Maryna Kobylynska, et al.
Human Genetics
|
November 11, 2010
Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots
Andreas Walter Kuss, Masoud Garshasbi, Kimia Kahrizi, et al.
European Journal of Human Genetics : EJHG
|
April 10, 2008
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression
Suzanna Gerarda Maria Frints, Steffen Lenzner, Mareike Bauters, et al.
Biological Psychiatry
|
October 8, 2015
Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort
Birgitte Bertelsen, Hreinn Stefánsson, Lars Riff Jensen, et al.
Nature
|
September 23, 2011
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
Hossein Najmabadi, Hao Hu, Masoud Garshasbi, et al.
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of 9
Search research articles
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Showing results (81-90 of 86) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 86 results.
The Plant Cell
|
February 22, 2019
Regulation of Oxygenic Photosynthesis during Trophic Transitions in the Green Alga <i>Chromochloris zofingiensis</i>
Melissa S Roth, Sean D Gallaher, Daniel J Westcott, et al.
Scientific Reports
|
November 27, 2025
Demonstrating soft X-ray tomography in the lab for correlative cryogenic biological imaging using X-rays and light microscopy
Stephen O'Connor, David Rogers, Maryna Kobylynska, et al.
Human Genetics
|
November 11, 2010
Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots
Andreas Walter Kuss, Masoud Garshasbi, Kimia Kahrizi, et al.
European Journal of Human Genetics : EJHG
|
April 10, 2008
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression
Suzanna Gerarda Maria Frints, Steffen Lenzner, Mareike Bauters, et al.
Biological Psychiatry
|
October 8, 2015
Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort
Birgitte Bertelsen, Hreinn Stefánsson, Lars Riff Jensen, et al.
Nature
|
September 23, 2011
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
Hossein Najmabadi, Hao Hu, Masoud Garshasbi, et al.
Page
of 9