asparagine and Abnormalities, Multiple

asparagine has been researched along with Abnormalities, Multiple in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (66.67)	29.6817
2010's	1 (33.33)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
de Koning, TJ	1
Anckarsäter, H; Betancur, C; Buxbaum, JD; Cai, G; Chaste, P; Gillberg, C; Goldsmith, J; Hollander, E; Leboyer, M; Nygren, G; Rastam, M; Reichert, J; Silverman, JM; Smith, CJ; Verloes, A	1
Campbell, RM; Dell, A; Ditto, D; Jaeken, J; Le, D; Levinson, SR; Long, JM; Marth, JD; Morris, HR; Panico, M; Schachter, H; Sutton-Smith, M; Tan, J; Varki, NM; Wang, Y; Wynshaw-Boris, A	1

Reviews

1 review(s) available for asparagine and Abnormalities, Multiple

Article	Year
Amino acid synthesis deficiencies. Journal of inherited metabolic disease, 2017, Volume: 40, Issue:4 Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Asparagine; Brain Diseases; Central Nervous System; Fetal Growth Retardation; Glutamine; High-Throughput Nucleotide Sequencing; Humans; Ichthyosis; Limb Deformities, Congenital; Metabolic Diseases; Mice; Microcephaly; Proline; Serine	2017

Article

Year

Amino acid synthesis deficiencies.

Journal of inherited metabolic disease, 2017, Volume: 40, Issue:4

Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Asparagine; Brain Diseases; Central Nervous System; Fetal Growth Retardation; Glutamine; High-Throughput Nucleotide Sequencing; Humans; Ichthyosis; Limb Deformities, Congenital; Metabolic Diseases; Mice; Microcephaly; Proline; Serine

2017

Other Studies

2 other study(ies) available for asparagine and Abnormalities, Multiple

Article	Year
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2007, Jun-05, Volume: 144B, Issue:4 Topics: Abnormalities, Multiple; Adolescent; Adult; Amino Acid Sequence; Asparagine; Aspartic Acid; Autistic Disorder; Child; Child, Preschool; Craniofacial Abnormalities; DNA Mutational Analysis; Exons; Female; Genetic Testing; Humans; Introns; Male; Molecular Sequence Data; Mutation; PTEN Phosphohydrolase; Syndrome	2007
Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesis. Glycobiology, 2001, Volume: 11, Issue:12 Topics: Abnormalities, Multiple; Animals; Asparagine; Bone Diseases, Metabolic; Congenital Disorders of Glycosylation; Disease Models, Animal; Glomerulonephritis; Glycosylation; Humans; Male; Mice; Mice, Inbred ICR; Mice, Mutant Strains; Mutation; N-Acetylglucosaminyltransferases; Polysaccharides; Species Specificity; Testis; Tissue Distribution	2001

Article

Year

Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2007, Jun-05, Volume: 144B, Issue:4

Topics: Abnormalities, Multiple; Adolescent; Adult; Amino Acid Sequence; Asparagine; Aspartic Acid; Autistic Disorder; Child; Child, Preschool; Craniofacial Abnormalities; DNA Mutational Analysis; Exons; Female; Genetic Testing; Humans; Introns; Male; Molecular Sequence Data; Mutation; PTEN Phosphohydrolase; Syndrome

2007

Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesis.

Glycobiology, 2001, Volume: 11, Issue:12

Topics: Abnormalities, Multiple; Animals; Asparagine; Bone Diseases, Metabolic; Congenital Disorders of Glycosylation; Disease Models, Animal; Glomerulonephritis; Glycosylation; Humans; Male; Mice; Mice, Inbred ICR; Mice, Mutant Strains; Mutation; N-Acetylglucosaminyltransferases; Polysaccharides; Species Specificity; Testis; Tissue Distribution

2001