proline and Osteomyelitis

proline has been researched along with Osteomyelitis 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
Duan, X; Mao, T; Wang, W; Xue, Y	1
Bing, X; El-Shanti, H; Ferguson, PJ; Mahgoub, A; Ochoa, LA; Schlueter, AJ; Tygrett, LT; Vasef, MA; Waldschmidt, TJ	1

Other Studies

2 other study(ies) available for proline and Osteomyelitis

Article	Year
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
A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis. Bone, 2006, Volume: 38, Issue:1 Topics: Adaptor Proteins, Signal Transducing; Amino Acid Sequence; Amino Acid Substitution; Animals; Autoimmune Diseases; Chromosome Mapping; Chromosomes, Mammalian; Chronic Disease; Crosses, Genetic; Cytoskeletal Proteins; DNA Mutational Analysis; Exons; Female; Genetic Markers; Inflammation; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Microsatellite Repeats; Molecular Sequence Data; Mutation, Missense; Osteomyelitis; Proline	2006

Article

Year

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

A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis.

Bone, 2006, Volume: 38, Issue:1

Topics: Adaptor Proteins, Signal Transducing; Amino Acid Sequence; Amino Acid Substitution; Animals; Autoimmune Diseases; Chromosome Mapping; Chromosomes, Mammalian; Chronic Disease; Crosses, Genetic; Cytoskeletal Proteins; DNA Mutational Analysis; Exons; Female; Genetic Markers; Inflammation; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Microsatellite Repeats; Molecular Sequence Data; Mutation, Missense; Osteomyelitis; Proline

2006