glutamic acid and Hyperlipoproteinemia Type II

glutamic acid has been researched along with Hyperlipoproteinemia Type II in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's4 (66.67)18.2507
2000's2 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cohen, JC; Gupta, S; He, G; Hobbs, HH; Michaely, P; Yi, M1
Knight, BL; Patel, DD; Soutar, AK1
Andresen, BS; Bolund, L; Hansen, AB; Hansen, PS; Jensen, HK; Jensen, LG; Jensen, TG; Kjeldsen, M; Meinertz, H; Nielsen, V1
Bertolini, S; Calandra, S; Cortese, C; Federici, G; Liberatoscioli, L; Motti, C; Rampa, P; Trovatello, G1
Blacklow, SC; North, CL1
Knight, BL; McCarthy, SN; Patel, DD; Soutar, AK; Sun, XM; Webb, JC1

Other Studies

6 other study(ies) available for glutamic acid and Hyperlipoproteinemia Type II

ArticleYear
ARH is a modular adaptor protein that interacts with the LDL receptor, clathrin, and AP-2.
    The Journal of biological chemistry, 2002, Nov-15, Volume: 277, Issue:46

    Topics: Adaptor Protein Complex 2; Adaptor Protein Complex beta Subunits; Adaptor Proteins, Signal Transducing; Adaptor Proteins, Vesicular Transport; Amino Acid Sequence; Animals; Binding Sites; Carrier Proteins; Clathrin; Endocytosis; Glutamic Acid; Glutathione Transferase; Humans; Hyperlipoproteinemia Type II; Immunoblotting; Mice; Models, Molecular; Molecular Sequence Data; Mutation; Plasmids; Protein Binding; Protein Structure, Tertiary; Receptors, LDL; Recombinant Fusion Proteins; Recombinant Proteins; Xenopus; Zebrafish

2002
Abnormal structure and co-operative binding of low-density lipoprotein receptors containing the Glu-80-->Lys mutation.
    Biochimica et biophysica acta, 1995, Apr-06, Volume: 1255, Issue:3

    Topics: Animals; Binding Sites; Cell Line; Cells, Cultured; Glutamic Acid; Haplorhini; Humans; Hyperlipoproteinemia Type II; Lysine; Mutagenesis, Site-Directed; Mutation; Neuraminidase; Pronase; Receptors, LDL

1995
Characterization of a disease-causing Glu119-Lys mutation in the low-density lipoprotein receptor gene in two Danish families with heterozygous familial hypercholesterolemia.
    Human mutation, 1994, Volume: 4, Issue:2

    Topics: Adult; Base Sequence; Female; Glutamic Acid; Humans; Hyperlipoproteinemia Type II; Lysine; Male; Middle Aged; Molecular Sequence Data; Mutagenesis, Site-Directed; Pedigree; Point Mutation; Polymerase Chain Reaction; Receptors, LDL

1994
Two novel mutations consisting in minor gene rearrangements in the human low density lipoprotein receptor gene in Italian patients affected by familial hypercholesterolemia. Mutations in brief no. 194. Online.
    Human mutation, 1998, Volume: 12, Issue:3

    Topics: Amino Acid Substitution; Cysteine; Frameshift Mutation; Glutamic Acid; Humans; Hyperlipoproteinemia Type II; Italy; Lysine; Receptors, LDL

1998
Solution structure of the sixth LDL-A module of the LDL receptor.
    Biochemistry, 2000, Mar-14, Volume: 39, Issue:10

    Topics: Amino Acid Sequence; Aspartic Acid; Calcium; Crystallography, X-Ray; Glutamic Acid; Humans; Hyperlipoproteinemia Type II; Lysine; Molecular Sequence Data; Mutagenesis, Site-Directed; Nuclear Magnetic Resonance, Biomolecular; Protein Binding; Protein Conformation; Protein Folding; Receptors, LDL; Solutions

2000
Characterization of two new point mutations in the low density lipoprotein receptor genes of an English patient with homozygous familial hypercholesterolemia.
    Journal of lipid research, 1992, Volume: 33, Issue:5

    Topics: Alleles; Amino Acid Sequence; Base Sequence; Cells, Cultured; Child, Preschool; England; Exons; Glutamates; Glutamic Acid; Homozygote; Humans; Hyperlipoproteinemia Type II; Lysine; Male; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Pedigree; Phenotype; Receptors, LDL

1992