Compounds > proline

proline and Elliptocytosis, Hereditary

proline has been researched along with Elliptocytosis, Hereditary in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fowler, PW; Reithmeier, RA; Sansom, MS1
Bhasin, N; Discher, DE; Gaetani, M; Gallagher, PG; Harper, S; Johnson, CP; Ortiz, V; Speicher, DW1
Alloisio, N; Dalla Venezia, N; Delaunay, J; Dhermy, D; Forissier, A; Garbarz, M; Morlé, L; Parquet, N; Rousset, T; Wilmotte, R1
Bloomberg, GB; Chambers, EJ; Ring, SM; Tanner, MJ1

Other Studies

4 other study(ies) available for proline and Elliptocytosis, Hereditary

ArticleYear
Effect of the Southeast Asian Ovalocytosis Deletion on the Conformational Dynamics of Signal-Anchor Transmembrane Segment 1 of Red Cell Anion Exchanger 1 (AE1, Band 3, or SLC4A1).
    Biochemistry, 2017, 02-07, Volume: 56, Issue:5

    Topics: Amino Acid Sequence; Anion Exchange Protein 1, Erythrocyte; Base Sequence; Elliptocytosis, Hereditary; Erythrocytes; Gene Expression; Humans; Hydrophobic and Hydrophilic Interactions; Membranes, Artificial; Molecular Dynamics Simulation; Phosphatidylcholines; Proline; Protein Domains; Protein Folding; Protein Structure, Secondary; Sequence Deletion

2017
Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding.
    Blood, 2007, Apr-15, Volume: 109, Issue:8

    Topics: Elliptocytosis, Hereditary; Humans; Mutation, Missense; Proline; Protein Folding; Spectrin; Spherocytosis, Hereditary

2007
An alpha-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the alpha v/41 polymorphism.
    Human genetics, 1993, Volume: 90, Issue:6

    Topics: Alleles; Base Sequence; DNA Mutational Analysis; Elliptocytosis, Hereditary; Female; Gene Expression; Heterozygote; Humans; Infant; Leucine; Male; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Spectrin

1993
Structural studies on the effects of the deletion in the red cell anion exchanger (band 3, AE1) associated with South East Asian ovalocytosis.
    Journal of molecular biology, 1999, Jan-22, Volume: 285, Issue:3

    Topics: Amides; Amino Acid Sequence; Anion Exchange Protein 1, Erythrocyte; Asia; Elliptocytosis, Hereditary; Humans; Magnetic Resonance Spectroscopy; Membrane Proteins; Microsomes; Models, Molecular; Molecular Conformation; Molecular Sequence Data; Peptide Fragments; Proline; Protein Biosynthesis; Protein Structure, Secondary; Sequence Alignment; Sequence Deletion

1999