glutamine and Broad Beta Disease

glutamine has been researched along with Broad Beta Disease in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Boomsma, DI; de Knijff, P; Frants, RR; Havekes, LM; Kastelein, JJ; Marais, AD; Smelt, AH; Stalenhoef, AF; van den Maagdenberg, AM	1
Brewer, HB; Lohse, P; Mann, WA; Stein, EA	1

Other Studies

2 other study(ies) available for glutamine and Broad Beta Disease

Article	Year
Variable expression of familial dysbetalipoproteinemia in apolipoprotein E2 (Lys146-->Gln) Allele carriers. The Journal of clinical investigation, 1994, Volume: 94, Issue:3* Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Amino Acid Sequence; Apolipoprotein E2; Apolipoproteins E; Base Sequence; Child; DNA Primers; Female; Gene Expression; Genetic Carrier Screening; Glutamine; Humans; Hyperlipoproteinemia Type III; Lysine; Male; Middle Aged; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction	1994
Apolipoprotein E-4Philadelphia (Glu13----Lys,Arg145----Cys). Homozygosity for two rare point mutations in the apolipoprotein E gene combined with severe type III hyperlipoproteinemia. The Journal of biological chemistry, 1991, Jun-05, Volume: 266, Issue:16 Topics: Adult; Amino Acid Sequence; Animals; Apolipoprotein E4; Apolipoproteins E; Arginine; Base Sequence; Cystine; DNA; Electrophoresis, Polyacrylamide Gel; Exons; Female; Glutamine; Humans; Hyperlipoproteinemia Type III; Lysine; Molecular Sequence Data; Mutation; Polymorphism, Restriction Fragment Length; Restriction Mapping	1991

Article

Year

Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriers.

The Journal of clinical investigation, 1994, Volume: 94, Issue:3

Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Amino Acid Sequence; Apolipoprotein E2; Apolipoproteins E; Base Sequence; Child; DNA Primers; Female; Gene Expression; Genetic Carrier Screening; Glutamine; Humans; Hyperlipoproteinemia Type III; Lysine; Male; Middle Aged; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction

1994

Apolipoprotein E-4Philadelphia (Glu13----Lys,Arg145----Cys). Homozygosity for two rare point mutations in the apolipoprotein E gene combined with severe type III hyperlipoproteinemia.

The Journal of biological chemistry, 1991, Jun-05, Volume: 266, Issue:16

Topics: Adult; Amino Acid Sequence; Animals; Apolipoprotein E4; Apolipoproteins E; Arginine; Base Sequence; Cystine; DNA; Electrophoresis, Polyacrylamide Gel; Exons; Female; Glutamine; Humans; Hyperlipoproteinemia Type III; Lysine; Molecular Sequence Data; Mutation; Polymorphism, Restriction Fragment Length; Restriction Mapping

1991