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Molecular Medicine Reports, ISSN 1791-2997, 12/2018, Volume 18, Issue 6, pp. 4865 - 4876
Cytochrome P450 family 4 (CYP4) enzymes are known as microsomal omega ()-hydroxylases that metabolize fatty acids, eicosanoids, vitamin D and carcinogens.... 
Hepatocellular carcinoma | Prognosis | Diagnosis | Cytochrome P450 family 4 | MEDICINE, RESEARCH & EXPERIMENTAL | diagnosis | PATTERNS | prognosis | cytochrome P450 family 4 | BREAST-CANCER | METABOLISM | ONCOLOGY | CYP4V2 | ENZYMES | hepatocellular carcinoma | PROGRESSION | SUBFAMILY | Immunohistochemistry | Carcinoma, Hepatocellular - mortality | Multigene Family | Liver Neoplasms - genetics | Humans | Middle Aged | RNA, Messenger - genetics | Gene Expression Regulation, Neoplastic | Transcriptome | Male | Gene Expression Profiling | Liver Neoplasms - mortality | Cytochrome P450 Family 4 - metabolism | Neoplasm Grading | Carcinoma, Hepatocellular - genetics | Carcinoma, Hepatocellular - pathology | Liver Neoplasms - metabolism | Adult | Female | Liver Neoplasms - pathology | Aged | Neoplasm Staging | Carcinoma, Hepatocellular - metabolism | Cytochrome P450 Family 4 - genetics | Genetic aspects | Research | Hepatoma | Gene expression | Cytochrome P-450 | Cytochrome | Eicosanoids | Infections | Genomes | Multivariate analysis | Medical diagnosis | Clinical outcomes | Metastases | Confidence intervals | Variables | Liver cancer | Hepatitis | Carcinogens | Vitamin D | Cell cycle | Enzymes | Cytochrome P450 | Fatty acids | Survival analysis | Medical prognosis | Protein expression | Software | Viral infections | Index Medicus
Journal Article
International Ophthalmology, ISSN 0165-5701, 6/2013, Volume 33, Issue 3, pp. 269 - 276
Bietti crystalline corneoretinal dystrophy (BCD, MIM 210370) is a type of hereditary retinal disorder which commonly occurs in China. It is known that... 
Ophthalmology | Medicine & Public Health | Bietti crystalline dystrophy | CYP4V2 gene
Journal Article
Clinical Ophthalmology, ISSN 1177-5483, 07/2019, Volume 13, pp. 1379 - 1399
GP García-García,1 M Martínez-Rubio,1 MA Moya-Moya,1 JJ Pérez-Santonja,1 J Escribano2,31Department of Ophthalmology, General University Hospital of Alicante,... 
retinal deposits | corneal deposits | Bietti crystalline dystrophy | CYP4V2 gene
Journal Article
Case Reports in Ophthalmology, 09/2011, Volume 2, Issue 3, pp. 296 - 301
To describe the clinical and genetic characteristics of a Japanese family in which one member exhibited Bietti's crystalline corneoretinal dystrophy (BCD).... 
Bietti's crystalline corneoretinal dystrophy | Retinitis pigmentosa | Retinal dystrophy | CYP4V2 gene
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, pp. e94960 - e94960
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2018, Volume 115, Issue 15, pp. 3936 - 3941
Journal Article
Journal Article
国际眼科杂志:英文版, ISSN 2222-3959, 2015, Volume 8, Issue 3, pp. 465 - 469
AIM: To analyze the CYP4V2 mutations in five unrelated Chinese patients with Bietti crystalline corneoretinal dystrophy(BCD) and to provide clinical features... 
corneoretinal | mutation | dystrophy | gene | CYP4V2 | Bietti’s | Bietti’s dystrophy | Corneoretinal dystrophy | Mutation | CYP4V2 gene | GENE | FAMILIES | OPHTHALMOLOGY | RETINOPATHY | CHOROIDAL NEOVASCULARIZATION | IDENTIFICATION | comeoretinal dystrophy | Bietti's dystrophy | corneoretinal dystrophy
Journal Article
The British journal of ophthalmology, ISSN 0007-1161, 02/2018, Volume 102, Issue 2, pp. 187 - 194
Journal Article
Case Reports in Ophthalmology, ISSN 1663-2699, 09/2011, Volume 2, Issue 3, pp. 296 - 301
Purpose: To describe the clinical and genetic characteristics of a Japanese family in which one member exhibited Bietti’s crystalline corneoretinal dystrophy... 
Published: September 2011 | Biettiߣs crystalline corneoretinal dystrophy | Retinitis pigmentosa | Retinal dystrophy | CYP4V2 gene
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 04/2018, Volume 115, Issue 15, pp. 3936 - 3941
Journal Article
Journal of Ophthalmology, ISSN 2090-004X, 2017, Volume 2017, pp. 4156386 - 4156386
Purpose. To characterize the clinical and molecular genetic characteristics of a large, multigenerational Chinese family showing different phenotypes. Methods.... 
MEDICINE, RESEARCH & EXPERIMENTAL | HPRP3 | OPHTHALMOLOGY | PRPF31 | MUTATIONS | SPLICING-FACTOR GENES | JAPANESE PATIENTS | IDENTIFICATION | CYP4V2 GENE | SPANISH FAMILIES | Family | Genetic aspects | Nucleotide sequencing | Cytochrome P-450 | Medical genetics | DNA sequencing
Journal Article
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