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Human Mutation
|
January 19, 2008
Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system
Gloria Hsi, Lara M Cullen, Georgina Macintyre, et al.
Lancet (London, England)
|
October 4, 1986
Prenatal diagnosis of alpha 1-antitrypsin deficiency by restriction fragment length polymorphisms, and comparison with oligonucleotide probe analysis
J F Hejtmancik, R N Sifers, P A Ward, et al.
Journal of Thoracic Imaging
|
October 26, 2013
The dark lymph node sign on magnetic resonance imaging: a novel finding in patients with sarcoidosis
Jonathan H Chung, Christian W Cox, Anna V Forssen, et al.
Microbiome
|
January 21, 2017
A fast and robust protocol for metataxonomic analysis using RNAseq data
Jeremy W Cox, Richard A Ballweg, Diana H Taft, et al.
American Journal of Obstetrics and Gynecology
|
April 15, 1981
Neonatal body water turnover: a putative index of perinatal morbidity
A H MacLennan, G Millington, A Grieve, et al.
Thorax
|
June 4, 2014
A longitudinal study of lung function from 1 month to 18 years of age
Steve Turner, Shona Fielding, Dave Mullane, et al.
Annals of Vascular Surgery
|
February 2, 2015
Spliced arm vein grafts are a durable conduit for lower extremity bypass
Katharine L McGinigle, Luigi Pascarella, Cynthia K Shortell, et al.
Nano Letters
|
November 3, 2018
Defect Manipulation To Control ZnO Micro-/Nanowire-Metal Contacts
Jonathan W Cox, Geoffrey M Foster, Alexander Jarjour, et al.
European Journal of Gastroenterology & Hepatology
|
May 8, 2001
Genotype-phenotype interactions in Wilson's disease: insight from an Icelandic mutation
R Palsson, J G Jonasson, M Kristjansson, et al.
Neuroimage
|
October 24, 2021
Trial and error: A hierarchical modeling approach to test-retest reliability
Gang Chen, Daniel S Pine, Melissa A Brotman, et al.
Page
of 73
Search research articles
Search
Showing results (471-480 of 725) with videos related to
Sort By:
Page
of 73
Human Mutation
|
January 19, 2008
Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system
Gloria Hsi, Lara M Cullen, Georgina Macintyre, et al.
Lancet (London, England)
|
October 4, 1986
Prenatal diagnosis of alpha 1-antitrypsin deficiency by restriction fragment length polymorphisms, and comparison with oligonucleotide probe analysis
J F Hejtmancik, R N Sifers, P A Ward, et al.
Journal of Thoracic Imaging
|
October 26, 2013
The dark lymph node sign on magnetic resonance imaging: a novel finding in patients with sarcoidosis
Jonathan H Chung, Christian W Cox, Anna V Forssen, et al.
Microbiome
|
January 21, 2017
A fast and robust protocol for metataxonomic analysis using RNAseq data
Jeremy W Cox, Richard A Ballweg, Diana H Taft, et al.
American Journal of Obstetrics and Gynecology
|
April 15, 1981
Neonatal body water turnover: a putative index of perinatal morbidity
A H MacLennan, G Millington, A Grieve, et al.
Thorax
|
June 4, 2014
A longitudinal study of lung function from 1 month to 18 years of age
Steve Turner, Shona Fielding, Dave Mullane, et al.
Annals of Vascular Surgery
|
February 2, 2015
Spliced arm vein grafts are a durable conduit for lower extremity bypass
Katharine L McGinigle, Luigi Pascarella, Cynthia K Shortell, et al.
Nano Letters
|
November 3, 2018
Defect Manipulation To Control ZnO Micro-/Nanowire-Metal Contacts
Jonathan W Cox, Geoffrey M Foster, Alexander Jarjour, et al.
European Journal of Gastroenterology & Hepatology
|
May 8, 2001
Genotype-phenotype interactions in Wilson's disease: insight from an Icelandic mutation
R Palsson, J G Jonasson, M Kristjansson, et al.
Neuroimage
|
October 24, 2021
Trial and error: A hierarchical modeling approach to test-retest reliability
Gang Chen, Daniel S Pine, Melissa A Brotman, et al.
Page
of 73