glutamic acid and Microcephaly

glutamic acid has been researched along with Microcephaly in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kiess, W; Klammt, J; Kratzsch, J; Kruis, T; Müller, E; Pfäffle, R; Schlicke, M; Schmidt, G; van de Leur, HS; Wallborn, T; Wüller, S	1
Breuning, MH; Kant, SG; Karperien, M; Kruithof, MF; Pereira, AM; Romijn, JA; van der Kamp, HJ; van Duyvenvoorde, HA; Walenkamp, MJ; Wit, JM	1

Other Studies

2 other study(ies) available for glutamic acid and Microcephaly

Article	Year
A heterozygous mutation of the insulin-like growth factor-I receptor causes retention of the nascent protein in the endoplasmic reticulum and results in intrauterine and postnatal growth retardation. The Journal of clinical endocrinology and metabolism, 2010, Volume: 95, Issue:5 Topics: Amino Acid Substitution; Birth Weight; Body Size; Cognition Disorders; Endoplasmic Reticulum; Exons; Female; Fetal Growth Retardation; Glutamic Acid; Growth Disorders; Heterozygote; Humans; Infant, Newborn; Insulin-Like Growth Factor Binding Protein 3; Insulin-Like Growth Factor I; Intellectual Disability; Microcephaly; Mutation, Missense; Polymerase Chain Reaction; Receptor, IGF Type 1; Valine	2010
A variable degree of intrauterine and postnatal growth retardation in a family with a missense mutation in the insulin-like growth factor I receptor. The Journal of clinical endocrinology and metabolism, 2006, Volume: 91, Issue:8 Topics: Adult; Base Sequence; Body Height; Bone Density; DNA Mutational Analysis; DNA, Complementary; Failure to Thrive; Female; Fetal Growth Retardation; Fibroblasts; Glutamic Acid; Growth Disorders; Heterozygote; Humans; Infant; Insulin-Like Growth Factor I; Lysine; Microcephaly; Mutation, Missense; Phosphorylation; Polymerase Chain Reaction; Receptor, IGF Type 1; Sequence Analysis, DNA; Signal Transduction	2006

Article

Year

A heterozygous mutation of the insulin-like growth factor-I receptor causes retention of the nascent protein in the endoplasmic reticulum and results in intrauterine and postnatal growth retardation.

The Journal of clinical endocrinology and metabolism, 2010, Volume: 95, Issue:5

Topics: Amino Acid Substitution; Birth Weight; Body Size; Cognition Disorders; Endoplasmic Reticulum; Exons; Female; Fetal Growth Retardation; Glutamic Acid; Growth Disorders; Heterozygote; Humans; Infant, Newborn; Insulin-Like Growth Factor Binding Protein 3; Insulin-Like Growth Factor I; Intellectual Disability; Microcephaly; Mutation, Missense; Polymerase Chain Reaction; Receptor, IGF Type 1; Valine

2010

A variable degree of intrauterine and postnatal growth retardation in a family with a missense mutation in the insulin-like growth factor I receptor.

The Journal of clinical endocrinology and metabolism, 2006, Volume: 91, Issue:8

Topics: Adult; Base Sequence; Body Height; Bone Density; DNA Mutational Analysis; DNA, Complementary; Failure to Thrive; Female; Fetal Growth Retardation; Fibroblasts; Glutamic Acid; Growth Disorders; Heterozygote; Humans; Infant; Insulin-Like Growth Factor I; Lysine; Microcephaly; Mutation, Missense; Phosphorylation; Polymerase Chain Reaction; Receptor, IGF Type 1; Sequence Analysis, DNA; Signal Transduction

2006