arginine and Osteopetrosis

arginine has been researched along with Osteopetrosis in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (50.00)	29.6817
2010's	2 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Liu, J; Pei, D; Shu, X; Wang, Q; Xu, J; Xu, T; Ye, Y	1
Abinun, M; Cassani, B; Clayton-Smith, J; Coxon, FP; Crockett, JC; Frattini, A; Guerrini, MM; Helfrich, MH; Kilic, SS; Mazzolari, E; Mellis, D; Moratto, D; Notarangelo, LD; Orchard, P; Pangrazio, A; Rogers, MJ; Sobacchi, C; Tezcan, I; Vellodi, A; Vezzoni, P; Villa, A	1
Duan, X; Mao, T; Wang, W; Xue, Y	1
Higashibata, Y; Nomura, S; Oboki, K; Sakuma, T; Sato, M	1

Reviews

1 review(s) available for arginine and Osteopetrosis

Article	Year
Molecular cause of the severe functional deficiency in osteoclasts by an arginine deletion in the basic domain of Mi transcription factor. Journal of bone and mineral metabolism, 2001, Volume: 19, Issue:3 Topics: Active Transport, Cell Nucleus; Alleles; Animals; Arginine; Cell Nucleus; DNA-Binding Proteins; Gene Deletion; Helix-Loop-Helix Motifs; Heterozygote; Homozygote; Humans; Mice; Mice, Mutant Strains; Microphthalmia-Associated Transcription Factor; Osteoclasts; Osteopetrosis; Transcription Factors	2001

Article

Year

Molecular cause of the severe functional deficiency in osteoclasts by an arginine deletion in the basic domain of Mi transcription factor.

Journal of bone and mineral metabolism, 2001, Volume: 19, Issue:3

Topics: Active Transport, Cell Nucleus; Alleles; Animals; Arginine; Cell Nucleus; DNA-Binding Proteins; Gene Deletion; Helix-Loop-Helix Motifs; Heterozygote; Homozygote; Humans; Mice; Mice, Mutant Strains; Microphthalmia-Associated Transcription Factor; Osteoclasts; Osteopetrosis; Transcription Factors

2001

Other Studies

3 other study(ies) available for arginine and Osteopetrosis

Article	Year
Structure of human SNX10 reveals insights into its role in human autosomal recessive osteopetrosis. Proteins, 2014, Volume: 82, Issue:12 Topics: Amino Acid Sequence; Amino Acid Substitution; Arginine; Humans; MCF-7 Cells; Models, Molecular; Molecular Sequence Data; Mutation; Osteoclasts; Osteopetrosis; Protein Conformation; Protein Interaction Domains and Motifs; Protein Stability; Protein Structure, Tertiary; Protein Transport; Recombinant Proteins; Sequence Alignment; Sorting Nexins; Tyrosine; Vacuoles	2014
Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations. American journal of human genetics, 2008, Volume: 83, Issue:1 Topics: Acid Phosphatase; Actins; Agammaglobulinemia; Amino Acid Sequence; Amino Acid Substitution; Argentina; Arginine; Biopsy; Case-Control Studies; Cell Line, Transformed; Cell Proliferation; Cell Transformation, Viral; Cells, Cultured; Cohort Studies; Consanguinity; Cysteine; Dendrites; DNA Mutational Analysis; Female; Genes, Recessive; Herpesvirus 4, Human; Heterozygote; Homozygote; Humans; Ilium; Isoenzymes; Leukocyte Common Antigens; Leukocytes, Mononuclear; Lipopolysaccharides; Macrophage Colony-Stimulating Factor; Male; Models, Immunological; Molecular Sequence Data; Mutation, Missense; Osteoclasts; Osteopetrosis; Osteoprotegerin; Pakistan; Pedigree; Polymorphism, Genetic; Protein Structure, Tertiary; Radiography, Thoracic; RANK Ligand; Receptor Activator of Nuclear Factor-kappa B; Receptors, Vitronectin; Sequence Homology, Amino Acid; Tartrate-Resistant Acid Phosphatase; Turkey	2008
Report of two Chinese patients suffering from CLCN7-related osteopetrosis and root dysplasia. Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery, 2012, Volume: 40, Issue:5 Topics: Adult; Arginine; Bone Density; China; Chloride Channels; Dentofacial Deformities; Genes, Recessive; Genetic Variation; Heterozygote; Homozygote; Humans; Leucine; Male; Osteomyelitis; Osteopetrosis; Osteosclerosis; Phenotype; Point Mutation; Proline; Tooth Abnormalities; Tooth Root; Tooth, Unerupted; Tryptophan	2012