Page last updated: 2024-08-23

propiconazole and Genetic Predisposition

propiconazole has been researched along with Genetic Predisposition in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (37.50)29.6817
2010's4 (50.00)24.3611
2020's1 (12.50)2.80

Authors

AuthorsStudies
Huang, XM; Liu, Y; Sun, FY; Tang, DR; Wu, T; Yang, WC1
Kahana, A; Wu, CY1
Cui, Z; Ding, T; Du, Y; Gao, W; Wang, Y; Xu, Z; Zhao, T1
Ambroziak, U; Bednarczuk, T; Hasse-Lazar, K; Hyla-Klekot, L; Jarzab, B; Jurecka-Lubieniecka, B; Kolosza, Z; Kula, D; Ploski, R; Szymanski, K; Tukiendorf, A1
Bardi, KM; Brandon, CA; Marazita, ML; Martin, RA; Naidoo, SD; Neiswanger, K; Resick, JM; Weinberg, SM1
Chen, B; Fernando, R; Smith, TJ; Tsui, S1
Bhadelia, R; Erbay, SH; Oljeski, SA1
Maher, BS; Marazita, ML; Weinberg, SM1

Reviews

1 review(s) available for propiconazole and Genetic Predisposition

ArticleYear
Parental craniofacial morphology in cleft lip with or without cleft palate as determined by cephalometry: a meta-analysis.
    Orthodontics & craniofacial research, 2006, Volume: 9, Issue:1

    Topics: Case-Control Studies; Cephalometry; Cleft Lip; Cleft Palate; Face; Facial Bones; Fathers; Genetic Predisposition to Disease; Humans; Mandible; Mothers; Nasal Cavity; Orbit; Parents; Skull; Skull Base; Vertical Dimension

2006

Other Studies

7 other study(ies) available for propiconazole and Genetic Predisposition

ArticleYear
Mutations in MC4R facilitate the angiogenic activity in patients with orbital venous malformation.
    Experimental biology and medicine (Maywood, N.J.), 2020, Volume: 245, Issue:11

    Topics: Adult; Cell Cycle; Cell Proliferation; Endothelial Cells; Female; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mutation; Neovascularization, Physiologic; Orbit; Receptor, Melanocortin, Type 4; Vascular Malformations; Veins

2020
Geriatric patients are predisposed to strabismus following thyroid-related orbital decompression surgery: A multivariate analysis.
    Orbit (Amsterdam, Netherlands), 2017, Volume: 36, Issue:2

    Topics: Adult; Aged; Aging; Decompression, Surgical; Female; Genetic Predisposition to Disease; Geriatrics; Graves Ophthalmopathy; Humans; Male; Middle Aged; Multivariate Analysis; Orbit; Postoperative Complications; Retrospective Studies; Risk Factors; Strabismus

2017
NUT midline carcinoma in the right orbit: a case report.
    Cancer biology & therapy, 2019, Volume: 20, Issue:8

    Topics: Biopsy; Combined Modality Therapy; Female; Genetic Association Studies; Genetic Predisposition to Disease; Head and Neck Neoplasms; Humans; Magnetic Resonance Imaging; Middle Aged; Neoplasm Proteins; Nuclear Proteins; Oncogene Proteins; Orbit; Tomography, X-Ray Computed; Translocation, Genetic; Treatment Outcome

2019
Association between polymorphisms in the TSHR gene and Graves' orbitopathy.
    PloS one, 2014, Volume: 9, Issue:7

    Topics: Adult; Alleles; Female; Genetic Association Studies; Genetic Predisposition to Disease; Graves Ophthalmopathy; Humans; Inflammation; Male; Middle Aged; Orbit; Polymorphism, Single Nucleotide; Receptors, Thyrotropin; Risk Factors

2014
Face shape of unaffected parents with cleft affected offspring: combining three-dimensional surface imaging and geometric morphometrics.
    Orthodontics & craniofacial research, 2009, Volume: 12, Issue:4

    Topics: Case-Control Studies; Cephalometry; Cleft Lip; Cleft Palate; Face; Family Health; Female; Genetic Predisposition to Disease; Humans; Imaging, Three-Dimensional; Lip; Male; Maxillofacial Development; Nose; Orbit; Parents; Photogrammetry; Principal Component Analysis; Sex Factors; Vertical Dimension; Zygoma

2009
Divergent Sp1 protein levels may underlie differential expression of UDP-glucose dehydrogenase by fibroblasts: role in susceptibility to orbital Graves disease.
    The Journal of biological chemistry, 2011, Jul-08, Volume: 286, Issue:27

    Topics: Cells, Cultured; Dermis; Fibroblasts; Gene Expression Regulation, Enzymologic; Genetic Predisposition to Disease; Glucuronosyltransferase; Graves Ophthalmopathy; Humans; Hyaluronan Synthases; Hyaluronic Acid; Orbit; Response Elements; RNA, Messenger; Sp1 Transcription Factor; Uridine Diphosphate Glucose Dehydrogenase

2011
Rapid development of optic glioma in a patient with hybrid phakomatosis: neurofibromatosis type 1 and tuberous sclerosis.
    AJNR. American journal of neuroradiology, 2004, Volume: 25, Issue:1

    Topics: Female; Genes, Tumor Suppressor; Genetic Predisposition to Disease; Humans; Infant, Newborn; Magnetic Resonance Imaging; Neoplasms, Multiple Primary; Neurocutaneous Syndromes; Neurofibromatosis 1; Optic Nerve; Optic Nerve Glioma; Orbit; Orbital Neoplasms; Radiographic Image Enhancement; Tuberous Sclerosis

2004