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Blood
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December 1, 1983
Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin alpha-subunit
J Lawler, J Palek, S C Liu, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal
|
February 14, 2015
Tuning the pressure-induced superconductivity in Pd-substituted CeRhIn5
M Kratochvilova, K Uhlirova, J Prchal, et al.
Blood
|
January 1, 1981
Altered assembly of spectrin in red cell membranes in hereditary pyropoikilocytosis
J Palek, S C Liu, P Y Liu, et al.
Human Molecular Genetics
|
July 13, 1999
Full-length human L1 insertions retain the capacity for high frequency retrotransposition in cultured cells
M L Kimberland, V Divoky, J Prchal, et al.
Metabolic and Pediatric Ophthalmology
|
January 1, 1980
Diabetes and risk of cataract development
J Prchal, H Skalka, R S Clements, et al.
Biochemical and Biophysical Research Communications
|
November 15, 1983
Gas chromatographic/mass spectrometric evidence for the identification of a heptitol and an octitol in human and Octodon degu eye lenses
S A Barker, F P Fish, M Tomana, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal
|
January 17, 2022
La<sub>2</sub>Pd<sub>2</sub>In: superconductivity and lattice properties at ambient and elevated pressures
P Král, M Diviš, L Havela, et al.
American Journal of Hematology
|
December 1, 1995
Triosephosphate isomerase deficiency: repetitive occurrence of point mutation in amino acid 104 in multiple apparently unrelated families
A Schneider, B Westwood, C Yim, et al.
Proteins
|
September 1, 2016
Molecular aspects of the interaction between Mason-Pfizer monkey virus matrix protein and artificial phospholipid membrane
P Junková, J Prchal, V Spiwok, et al.
The Journal of Clinical Investigation
|
September 1, 1991
Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis
T L Coetzer, K Sahr, J Prchal, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
Blood
|
December 1, 1983
Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin alpha-subunit
J Lawler, J Palek, S C Liu, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal
|
February 14, 2015
Tuning the pressure-induced superconductivity in Pd-substituted CeRhIn5
M Kratochvilova, K Uhlirova, J Prchal, et al.
Blood
|
January 1, 1981
Altered assembly of spectrin in red cell membranes in hereditary pyropoikilocytosis
J Palek, S C Liu, P Y Liu, et al.
Human Molecular Genetics
|
July 13, 1999
Full-length human L1 insertions retain the capacity for high frequency retrotransposition in cultured cells
M L Kimberland, V Divoky, J Prchal, et al.
Metabolic and Pediatric Ophthalmology
|
January 1, 1980
Diabetes and risk of cataract development
J Prchal, H Skalka, R S Clements, et al.
Biochemical and Biophysical Research Communications
|
November 15, 1983
Gas chromatographic/mass spectrometric evidence for the identification of a heptitol and an octitol in human and Octodon degu eye lenses
S A Barker, F P Fish, M Tomana, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal
|
January 17, 2022
La<sub>2</sub>Pd<sub>2</sub>In: superconductivity and lattice properties at ambient and elevated pressures
P Král, M Diviš, L Havela, et al.
American Journal of Hematology
|
December 1, 1995
Triosephosphate isomerase deficiency: repetitive occurrence of point mutation in amino acid 104 in multiple apparently unrelated families
A Schneider, B Westwood, C Yim, et al.
Proteins
|
September 1, 2016
Molecular aspects of the interaction between Mason-Pfizer monkey virus matrix protein and artificial phospholipid membrane
P Junková, J Prchal, V Spiwok, et al.
The Journal of Clinical Investigation
|
September 1, 1991
Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis
T L Coetzer, K Sahr, J Prchal, et al.
Page
of 4