glutamine and Xeroderma

glutamine has been researched along with Xeroderma in 3 studies

Research

Studies (3)

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

Authors

Authors	Studies
de Koning, TJ	1
Fésüs, L; Marekov, LN; Nemes, Z; Steinert, PM	1
Ionasescu, V; Mueller, S; Stegink, L; Weinstein, M	1

Reviews

1 review(s) available for glutamine and Xeroderma

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 glutamine and Xeroderma

Article	Year
A novel function for transglutaminase 1: attachment of long-chain omega-hydroxyceramides to involucrin by ester bond formation. Proceedings of the National Academy of Sciences of the United States of America, 1999, Jul-20, Volume: 96, Issue:15 Topics: Amino Acid Sequence; Ceramides; Enzyme Inhibitors; Epidermis; Esterification; Glutamine; Humans; Ichthyosis; Mass Spectrometry; Molecular Sequence Data; Molecular Structure; Peptide Fragments; Protein Precursors; Putrescine; Recombinant Proteins; Sequence Analysis; Substrate Specificity; Transglutaminases; Trypsin	1999
Amino acid abnormality in Sjögren-Larsson syndrome. Archives of neurology, 1973, Volume: 28, Issue:3 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Dental Enamel Hypoplasia; Epilepsy; Ethylamines; Glutamine; Glycine; Histidine; Humans; Ichthyosis; Intellectual Disability; Isoleucine; Leucine; Lysine; Male; Muscle Spasticity; Retinal Degeneration; Serine; Syndrome; Valine	1973

Article

Year

A novel function for transglutaminase 1: attachment of long-chain omega-hydroxyceramides to involucrin by ester bond formation.

Proceedings of the National Academy of Sciences of the United States of America, 1999, Jul-20, Volume: 96, Issue:15

Topics: Amino Acid Sequence; Ceramides; Enzyme Inhibitors; Epidermis; Esterification; Glutamine; Humans; Ichthyosis; Mass Spectrometry; Molecular Sequence Data; Molecular Structure; Peptide Fragments; Protein Precursors; Putrescine; Recombinant Proteins; Sequence Analysis; Substrate Specificity; Transglutaminases; Trypsin

1999

Amino acid abnormality in Sjögren-Larsson syndrome.

Archives of neurology, 1973, Volume: 28, Issue:3

Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Dental Enamel Hypoplasia; Epilepsy; Ethylamines; Glutamine; Glycine; Histidine; Humans; Ichthyosis; Intellectual Disability; Isoleucine; Leucine; Lysine; Male; Muscle Spasticity; Retinal Degeneration; Serine; Syndrome; Valine

1973