arginine and Abnormalities, Teeth

arginine has been researched along with Abnormalities, Teeth in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (14.29)18.2507
2000's2 (28.57)29.6817
2010's4 (57.14)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Biedziak, B; JagodziƄski, PP; Matuszewska-Trojan, S; Mostowska, A; Zadurska, M1
Bailleul-Forestier, I; Bennaceur, S; de Roux, N; Gros, C; Leger, J; Zenaty, D1
Duan, X; Mao, T; Wang, W; Xue, Y1
Dingerdissen, H; Karagiannis, K; Mazumder, R; Motwani, M; Simonyan, V1
Aaltonen, M; Brunner, HG; Danesino, C; Duijf, P; Huoponen, K; Kjaer, KW; Kock, M; Larizza, D; Penttinen, M; Rinne, T; Savontaus, ML; Spadoni, E; van Bokhoven, H1
Abate-Shen, C; Bendall, AJ; Greenfield, N; Hu, G; Logan, M; Nelson, C; Seidman, CE; Seidman, JG; Stein, S; Vastardis, H; Wang, Z; Zhang, H1
Crocci, AJ; Lopes, LF; Minicucci, EM1

Other Studies

7 other study(ies) available for arginine and Abnormalities, Teeth

ArticleYear
WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.
    European journal of oral sciences, 2015, Volume: 123, Issue:1

    Topics: Adolescent; Adult; Anodontia; Arginine; Base Sequence; Child; Cohort Studies; Conserved Sequence; Cysteine; Female; Genetic Variation; Genotype; Humans; Incisor; Isoleucine; Leucine; Male; MSX1 Transcription Factor; Mutation; Open Reading Frames; PAX9 Transcription Factor; Phenylalanine; Polymorphism, Genetic; Tooth Abnormalities; Wnt Proteins; Young Adult

2015
Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations.
    International journal of paediatric dentistry, 2010, Volume: 20, Issue:4

    Topics: Adenine; Adolescent; Adult; Anodontia; Arginine; Bicuspid; Child, Preschool; Cleft Palate; Cysteine; Cytosine; Female; Glutamine; Glycine; Guanine; Humans; Incisor; Kallmann Syndrome; Male; Middle Aged; Molar; Mutation; Receptor, Fibroblast Growth Factor, Type 1; Sequence Deletion; Tooth Abnormalities; Tooth Root; Tooth, Deciduous; Tryptophan; Young Adult

2010
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
Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins.
    The FEBS journal, 2013, Volume: 280, Issue:6

    Topics: Abnormalities, Multiple; Amino Acid Substitution; Arginine; Aspartic Acid; Carbohydrate Metabolism; Catalytic Domain; Cluster Analysis; Enzyme Activation; Genetic Variation; Genome, Human; Glycogen Storage Disease; Hearing Loss; Histidine; Humans; Lacrimal Apparatus Diseases; Metabolomics; Molecular Sequence Annotation; Phenylalanine; Polymorphism, Single Nucleotide; Proteome; Proteomics; Structure-Activity Relationship; Syndactyly; Tooth Abnormalities; Tyrosine

2013
Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene.
    European journal of human genetics : EJHG, 2006, Volume: 14, Issue:8

    Topics: Abnormalities, Multiple; Adult; Arginine; Child; Ectodermal Dysplasia; Female; Genes, Tumor Suppressor; Humans; Limb Deformities, Congenital; Male; Middle Aged; Mutation, Missense; Phenotype; Syndrome; Tooth Abnormalities; Transcriptional Activation

2006
Haploinsufficiency of MSX1: a mechanism for selective tooth agenesis.
    Molecular and cellular biology, 1998, Volume: 18, Issue:10

    Topics: Amino Acid Substitution; Animals; Arginine; Binding Sites; Chickens; DNA; Extremities; Homeodomain Proteins; Humans; Mice; MSX1 Transcription Factor; Proline; Tooth Abnormalities; Transcription Factors

1998
Dental abnormalities in children after chemotherapy treatment for acute lymphoid leukemia.
    Leukemia research, 2003, Volume: 27, Issue:1

    Topics: Antineoplastic Combined Chemotherapy Protocols; Asparaginase; Child; Child, Preschool; Combined Modality Therapy; Cranial Irradiation; Cyclophosphamide; Cytarabine; Dental Enamel Hypoplasia; Dexamethasone; Doxorubicin; Etoposide; Female; Humans; Infant; Male; Mercaptopurine; Methotrexate; Odontogenesis; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Prednisone; Teniposide; Tooth Abnormalities; Tooth Diseases; Tooth Eruption; Tooth Root; Vincristine

2003