glutamine and Congenital Limb Deformities

glutamine has been researched along with Congenital Limb Deformities 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	1 (33.33)	29.6817
2010's	2 (66.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
de Koning, TJ	1
Doelken, SC; Hansen, P; Hecht, J; Horn, D; Ibrahim, DM; Jäger, M; Janetzki, C; Krawitz, P; Leschik, G; Mundlos, S; Robinson, PN; Rödelsperger, C; Scheuer, T; Schmidt-von Kegler, M; Seemann, P; Stiege, AC; Timmermann, B; Wagner, F	1
Hadzsiev, K; Kellermayer, R; Kestilä, M; Kosztolányi, G; Siitonen, HA	1

Reviews

1 review(s) available for glutamine and Congenital Limb Deformities

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 Congenital Limb Deformities

Article	Year
Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutations. Genome research, 2013, Volume: 23, Issue:12 Topics: Animals; Binding Sites; Chick Embryo; Chromatin Immunoprecipitation; Female; Gene Expression Profiling; Genome, Human; Glutamine; Homeodomain Proteins; Humans; Limb Deformities, Congenital; Mesenchymal Stem Cells; Mutation, Missense; Oligonucleotide Array Sequence Analysis; Paired Box Transcription Factors; Phenotype; Receptor Tyrosine Kinase-like Orphan Receptors; Transcription Factors	2013
A patient with Rothmund-Thomson syndrome and all features of RAPADILINO. Archives of dermatology, 2005, Volume: 141, Issue:5 Topics: Abnormalities, Multiple; Adenosine Triphosphatases; Amino Acid Substitution; Arginine; Bone and Bones; Child; Cytosine; Diarrhea; DNA Helicases; Glutamine; Growth Disorders; Guanine; Humans; Joint Dislocations; Limb Deformities, Congenital; Male; Mutation; Mutation, Missense; Palate; Patella; Radius; RecQ Helicases; Rothmund-Thomson Syndrome; Syndrome; Thymine	2005

Article

Year

Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutations.

Genome research, 2013, Volume: 23, Issue:12

Topics: Animals; Binding Sites; Chick Embryo; Chromatin Immunoprecipitation; Female; Gene Expression Profiling; Genome, Human; Glutamine; Homeodomain Proteins; Humans; Limb Deformities, Congenital; Mesenchymal Stem Cells; Mutation, Missense; Oligonucleotide Array Sequence Analysis; Paired Box Transcription Factors; Phenotype; Receptor Tyrosine Kinase-like Orphan Receptors; Transcription Factors

2013

A patient with Rothmund-Thomson syndrome and all features of RAPADILINO.

Archives of dermatology, 2005, Volume: 141, Issue:5

Topics: Abnormalities, Multiple; Adenosine Triphosphatases; Amino Acid Substitution; Arginine; Bone and Bones; Child; Cytosine; Diarrhea; DNA Helicases; Glutamine; Growth Disorders; Guanine; Humans; Joint Dislocations; Limb Deformities, Congenital; Male; Mutation; Mutation, Missense; Palate; Patella; Radius; RecQ Helicases; Rothmund-Thomson Syndrome; Syndrome; Thymine

2005