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Biochemical Society Transactions
|
August 17, 2016
Non-coding RNAs and disease: the classical ncRNAs make a comeback
Rogerio Alves de Almeida, Marcin G Fraczek, Steven Parker, et al.
Biochemical and Biophysical Research Communications
|
July 17, 2007
Analysis of pre-mRNA and pre-rRNA processing factor Snu13p structure and mutants
Helen C Dobbyn, Paul A McEwan, Andre Krause, et al.
Irish Medical Journal
|
November 14, 2013
The National Single Assessment Tool (SAT) a pilot study in older persons care-survey results
L McDermott-Scales, D Beaton, F McMahon, et al.
Clinical Genetics
|
April 20, 2018
A known pathogenic variant in the essential mitochondrial translation gene RMND1 causes a Perrault-like syndrome with renal defects
L A M Demain, D Antunes, J O'Sullivan, et al.
Genome Research
|
March 25, 2022
Global mapping of RNA homodimers in living cells
Marta M Gabryelska, Andrew P Badrock, Jian You Lau, et al.
Acta Crystallographica. Section E, Crystallographic Communications
|
August 7, 2024
Structural determination of oleanane-28,13β-olide and taraxerane-28,14β-olide fluoro-lactonization products from the reaction of oleanolic acid with Selectfluor<sup>TM</sup>
Megan A Eadsforth, Linghan Kong, George Whitehead, et al.
South Dakota Journal of Medicine
|
May 1, 1978
Just sign here
M Flanery, J Gravdal, P Hendrix, et al.
Reproductive Biomedicine Online
|
July 5, 2022
Homozygous missense variants in BMPR15 can result in primary ovarian insufficiency
Leigh A M Demain, Kay Metcalfe, Eline Boetje, et al.
Plos Genetics
|
January 25, 2021
Functional and transcriptional profiling of non-coding RNAs in yeast reveal context-dependent phenotypes and in trans effects on the protein regulatory network
Laura Natalia Balarezo-Cisneros, Steven Parker, Marcin G Fraczek, et al.
Journal of Human Genetics
|
December 13, 2019
A recurrent missense variant in HARS2 results in variable sensorineural hearing loss in three unrelated families
Leigh A M Demain, Erica H Gerkes, Richard J H Smith, et al.
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of 10
Search research articles
Search
Showing results (41-50 of 92) with videos related to
Sort By:
Page
of 10
Biochemical Society Transactions
|
August 17, 2016
Non-coding RNAs and disease: the classical ncRNAs make a comeback
Rogerio Alves de Almeida, Marcin G Fraczek, Steven Parker, et al.
Biochemical and Biophysical Research Communications
|
July 17, 2007
Analysis of pre-mRNA and pre-rRNA processing factor Snu13p structure and mutants
Helen C Dobbyn, Paul A McEwan, Andre Krause, et al.
Irish Medical Journal
|
November 14, 2013
The National Single Assessment Tool (SAT) a pilot study in older persons care-survey results
L McDermott-Scales, D Beaton, F McMahon, et al.
Clinical Genetics
|
April 20, 2018
A known pathogenic variant in the essential mitochondrial translation gene RMND1 causes a Perrault-like syndrome with renal defects
L A M Demain, D Antunes, J O'Sullivan, et al.
Genome Research
|
March 25, 2022
Global mapping of RNA homodimers in living cells
Marta M Gabryelska, Andrew P Badrock, Jian You Lau, et al.
Acta Crystallographica. Section E, Crystallographic Communications
|
August 7, 2024
Structural determination of oleanane-28,13β-olide and taraxerane-28,14β-olide fluoro-lactonization products from the reaction of oleanolic acid with Selectfluor<sup>TM</sup>
Megan A Eadsforth, Linghan Kong, George Whitehead, et al.
South Dakota Journal of Medicine
|
May 1, 1978
Just sign here
M Flanery, J Gravdal, P Hendrix, et al.
Reproductive Biomedicine Online
|
July 5, 2022
Homozygous missense variants in BMPR15 can result in primary ovarian insufficiency
Leigh A M Demain, Kay Metcalfe, Eline Boetje, et al.
Plos Genetics
|
January 25, 2021
Functional and transcriptional profiling of non-coding RNAs in yeast reveal context-dependent phenotypes and in trans effects on the protein regulatory network
Laura Natalia Balarezo-Cisneros, Steven Parker, Marcin G Fraczek, et al.
Journal of Human Genetics
|
December 13, 2019
A recurrent missense variant in HARS2 results in variable sensorineural hearing loss in three unrelated families
Leigh A M Demain, Erica H Gerkes, Richard J H Smith, et al.
Page
of 10