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Biochemical Pharmacology
|
November 13, 2016
Transcription factor binding site enrichment analysis predicts drivers of altered gene expression in nonalcoholic steatohepatitis
April D Lake, Alexandria L Chaput, Petr Novak, et al.
The British Journal of Dermatology
|
December 1, 1992
Restrictive dermopathy: a disorder of fibroblasts
D G Paige, B D Lake, A J Bailey, et al.
Annals of Biomedical Engineering
|
October 16, 2001
Comparison and clinical application of frequency domain methods in analysis of neonatal heart rate time series
K L Chang, K J Monahan, M P Griffin, et al.
Archives of Disease in Childhood
|
April 1, 1994
Laryngo-onycho-cutaneous syndrome: an inherited epithelial defect
R J Phillips, D J Atherton, M L Gibbs, et al.
Eye (London, England)
|
August 9, 2014
Sterile keratitis after combined riboflavin-UVA corneal collagen cross-linking for keratoconus
F C Lam, P Georgoudis, P Geourgoudis, et al.
Proteome Science
|
June 16, 2010
Development of high-yield autofluorescent protein microarrays using hybrid cell-free expression with combined Escherichia coli S30 and wheat germ extracts
Xristo Zárate, David C Henderson, Keenan C Phillips, et al.
Journal of the Optical Society of America. A, Optics, Image Science, and Vision
|
September 11, 2019
Improving holographic search algorithms using sorted pixel selection
Peter J Christopher, Jamie D Lake, Daoming Dong, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
January 19, 2017
Impaired N-linked glycosylation of uptake and efflux transporters in human non-alcoholic fatty liver disease
John D Clarke, Petr Novak, April D Lake, et al.
The Quarterly Journal of Medicine
|
January 1, 1971
Hepatic glycogen storage disease. Clinical and laboratory findings in 23 cases
J Spencer-Peet, M E Norman, B D Lake, et al.
Developmental Medicine and Child Neurology
|
February 1, 1983
Involvement of the central nervous system in congenital muscular dystrophies
J Egger, B E Kendall, M Erdohazi, et al.
Page
of 30
Search research articles
Search
Showing results (161-170 of 292) with videos related to
Sort By:
Page
of 30
Biochemical Pharmacology
|
November 13, 2016
Transcription factor binding site enrichment analysis predicts drivers of altered gene expression in nonalcoholic steatohepatitis
April D Lake, Alexandria L Chaput, Petr Novak, et al.
The British Journal of Dermatology
|
December 1, 1992
Restrictive dermopathy: a disorder of fibroblasts
D G Paige, B D Lake, A J Bailey, et al.
Annals of Biomedical Engineering
|
October 16, 2001
Comparison and clinical application of frequency domain methods in analysis of neonatal heart rate time series
K L Chang, K J Monahan, M P Griffin, et al.
Archives of Disease in Childhood
|
April 1, 1994
Laryngo-onycho-cutaneous syndrome: an inherited epithelial defect
R J Phillips, D J Atherton, M L Gibbs, et al.
Eye (London, England)
|
August 9, 2014
Sterile keratitis after combined riboflavin-UVA corneal collagen cross-linking for keratoconus
F C Lam, P Georgoudis, P Geourgoudis, et al.
Proteome Science
|
June 16, 2010
Development of high-yield autofluorescent protein microarrays using hybrid cell-free expression with combined Escherichia coli S30 and wheat germ extracts
Xristo Zárate, David C Henderson, Keenan C Phillips, et al.
Journal of the Optical Society of America. A, Optics, Image Science, and Vision
|
September 11, 2019
Improving holographic search algorithms using sorted pixel selection
Peter J Christopher, Jamie D Lake, Daoming Dong, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
January 19, 2017
Impaired N-linked glycosylation of uptake and efflux transporters in human non-alcoholic fatty liver disease
John D Clarke, Petr Novak, April D Lake, et al.
The Quarterly Journal of Medicine
|
January 1, 1971
Hepatic glycogen storage disease. Clinical and laboratory findings in 23 cases
J Spencer-Peet, M E Norman, B D Lake, et al.
Developmental Medicine and Child Neurology
|
February 1, 1983
Involvement of the central nervous system in congenital muscular dystrophies
J Egger, B E Kendall, M Erdohazi, et al.
Page
of 30