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Cold Spring Harbor Molecular Case Studies
|
August 24, 2016
Exome sequencing results in successful diagnosis and treatment of a severe congenital anemia
Jessica N Lacy, Jacob C Ulirsch, Rachael F Grace, et al.
Nature
|
June 21, 1990
Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8
S E Lux, W T Tse, J C Menninger, et al.
The Journal of Clinical Investigation
|
January 15, 1996
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis
P B Jenkins, G K Abou-Alfa, D Dhermy, et al.
The Journal of Clinical Investigation
|
June 8, 1999
Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice
L L Peters, H K Jindel, B Gwynn, et al.
ACS Synthetic Biology
|
March 11, 2024
Cell-Free Protein Expression in Polymer Materials
Marilyn S Lee, Jennifer A Lee, John R Biondo, et al.
Cell
|
September 20, 1996
Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton
L L Peters, R A Shivdasani, S C Liu, et al.
Schmerz (Berlin, Germany)
|
February 13, 2003
[Standardization of invasive neuromodulatory procedures]
H Harke, E Rosenow, V Tronnier, et al.
Nature Genetics
|
June 1, 1996
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis
S W Eber, J M Gonzalez, M L Lux, et al.
American Journal of Physiology. Cell Physiology
|
August 19, 2011
Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S
Andrew K Stewart, Boris E Shmukler, David H Vandorpe, et al.
Nature
|
February 29, 2000
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
A Donovan, A Brownlie, Y Zhou, et al.
Page
of 14
Search research articles
Search
Showing results (121-130 of 131) with videos related to
Sort By:
Page
of 14
Cold Spring Harbor Molecular Case Studies
|
August 24, 2016
Exome sequencing results in successful diagnosis and treatment of a severe congenital anemia
Jessica N Lacy, Jacob C Ulirsch, Rachael F Grace, et al.
Nature
|
June 21, 1990
Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8
S E Lux, W T Tse, J C Menninger, et al.
The Journal of Clinical Investigation
|
January 15, 1996
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis
P B Jenkins, G K Abou-Alfa, D Dhermy, et al.
The Journal of Clinical Investigation
|
June 8, 1999
Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice
L L Peters, H K Jindel, B Gwynn, et al.
ACS Synthetic Biology
|
March 11, 2024
Cell-Free Protein Expression in Polymer Materials
Marilyn S Lee, Jennifer A Lee, John R Biondo, et al.
Cell
|
September 20, 1996
Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton
L L Peters, R A Shivdasani, S C Liu, et al.
Schmerz (Berlin, Germany)
|
February 13, 2003
[Standardization of invasive neuromodulatory procedures]
H Harke, E Rosenow, V Tronnier, et al.
Nature Genetics
|
June 1, 1996
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis
S W Eber, J M Gonzalez, M L Lux, et al.
American Journal of Physiology. Cell Physiology
|
August 19, 2011
Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S
Andrew K Stewart, Boris E Shmukler, David H Vandorpe, et al.
Nature
|
February 29, 2000
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
A Donovan, A Brownlie, Y Zhou, et al.
Page
of 14