arginine and Craniofacial Abnormalities

arginine has been researched along with Craniofacial Abnormalities 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
Bunte, R; Guo, C; He, W; Kashina, A; Kurosaka, S; Leu, NA; Saha, S; Wang, J; Zhang, F	1
Brown, CA; Lupski, JR; Potocki, L; Shen, JJ	1

Other Studies

2 other study(ies) available for arginine and Craniofacial Abnormalities

Article	Year
Arginylation-dependent neural crest cell migration is essential for mouse development. PLoS genetics, 2010, Mar-12, Volume: 6, Issue:3 Topics: Aminoacyltransferases; Animals; Animals, Newborn; Arginine; Bone and Bones; Cell Adhesion; Cell Movement; Cells, Cultured; Coculture Techniques; Craniofacial Abnormalities; Gene Knockout Techniques; Growth and Development; Mesoderm; Mice; Mice, Knockout; Models, Biological; Neural Crest; Palate; Survival Analysis; Wnt1 Protein	2010
Mandibuloacral dysplasia caused by homozygosity for the R527H mutation in lamin A/C. Journal of medical genetics, 2003, Volume: 40, Issue:11 Topics: Abnormalities, Multiple; Adolescent; Amino Acid Substitution; Arginine; Craniofacial Abnormalities; Genes, Recessive; Genotype; Histidine; Homozygote; Humans; Lamin Type A; Lipodystrophy; Male; Musculoskeletal Abnormalities; Mutation; Phenotype	2003

Article

Year

Arginylation-dependent neural crest cell migration is essential for mouse development.

PLoS genetics, 2010, Mar-12, Volume: 6, Issue:3

Topics: Aminoacyltransferases; Animals; Animals, Newborn; Arginine; Bone and Bones; Cell Adhesion; Cell Movement; Cells, Cultured; Coculture Techniques; Craniofacial Abnormalities; Gene Knockout Techniques; Growth and Development; Mesoderm; Mice; Mice, Knockout; Models, Biological; Neural Crest; Palate; Survival Analysis; Wnt1 Protein

2010

Mandibuloacral dysplasia caused by homozygosity for the R527H mutation in lamin A/C.

Journal of medical genetics, 2003, Volume: 40, Issue:11

Topics: Abnormalities, Multiple; Adolescent; Amino Acid Substitution; Arginine; Craniofacial Abnormalities; Genes, Recessive; Genotype; Histidine; Homozygote; Humans; Lamin Type A; Lipodystrophy; Male; Musculoskeletal Abnormalities; Mutation; Phenotype

2003