Compounds > leucine

leucine and Craniofacial Abnormalities

leucine has been researched along with Craniofacial Abnormalities in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gerton, JL; Lee, KK; Xu, B; Zhang, L1
Gaudenz, K; Gerton, JL; Gogol, M; Xu, B1
Dressler, P; Hartmann, J; Meyer-Marcotty, P; Stellzig-Eisenhauer, A; Weisschuh, N1

Other Studies

3 other study(ies) available for leucine and Craniofacial Abnormalities

ArticleYear
Stimulation of mTORC1 with L-leucine rescues defects associated with Roberts syndrome.
    PLoS genetics, 2013, Volume: 9, Issue:10

    Topics: Acetyltransferases; Animals; Cell Cycle Proteins; Chromosomal Proteins, Non-Histone; Chromosome Segregation; Cohesins; Craniofacial Abnormalities; Ectromelia; Embryonic Development; Humans; Hypertelorism; Leucine; Mechanistic Target of Rapamycin Complex 1; Multiprotein Complexes; RNA, Ribosomal; Signal Transduction; TOR Serine-Threonine Kinases; Tumor Suppressor Protein p53; Zebrafish

2013
Improved transcription and translation with L-leucine stimulation of mTORC1 in Roberts syndrome.
    BMC genomics, 2016, Jan-05, Volume: 17

    Topics: Acetyltransferases; Animals; Chromosomal Proteins, Non-Histone; Craniofacial Abnormalities; Disease Models, Animal; Ectromelia; Humans; Hypertelorism; Leucine; Mutation; Protein Biosynthesis; Ribosomes; TOR Serine-Threonine Kinases; Transcription, Genetic; Zebrafish

2016
Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2008, Volume: 37, Issue:8

    Topics: Adolescent; Cephalometry; Chromosomes, Human, Pair 13; Codon; Cranial Fossa, Posterior; Craniofacial Abnormalities; Cytosine; Eye Abnormalities; Facial Bones; Female; Forkhead Transcription Factors; Heterozygote; Homeobox Protein PITX2; Homeodomain Proteins; Humans; Leucine; Male; Malocclusion, Angle Class III; Maxilla; Middle Aged; Mutation, Missense; Proline; Sella Turcica; Syndrome; Thymine; Tooth Abnormalities; Transcription Factors; Young Adult

2008