Literature DB >> 21851494

Miller syndrome with novel dihydroorotate dehydrogenase gene mutations.

Fumiko Kinoshita1, Tatsuro Kondoh, Kazuhiro Komori, Takeshi Matsui, Naoki Harada, Akinori Yanai, Masafumi Fukuda, Kanako Morifuji, Tadashi Matsumoto.   

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Year:  2011        PMID： 21851494     DOI： 10.1111/j.1442-200X.2010.03303.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN： 1328-8067            Impact factor:   1.524


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  7 in total

1.  Cross-Cancer Pleiotropic Associations with Lung Cancer Risk in African Americans.

Authors:  Carissa C Jones; Yuki Bradford; Christopher I Amos; William J Blot; Stephen J Chanock; Curtis C Harris; Ann G Schwartz; Margaret R Spitz; John K Wiencke; Margaret R Wrensch; Xifeng Wu; Melinda C Aldrich
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2019-03-20       Impact factor: 4.254

Review 2.  DHODH and cancer: promising prospects to be explored.

Authors:  Yue Zhou; Lei Tao; Xia Zhou; Zeping Zuo; Jin Gong; Xiaocong Liu; Yang Zhou; Chunqi Liu; Na Sang; Huan Liu; Jiao Zou; Kun Gou; Xiaowei Yang; Yinglan Zhao
Journal:  Cancer Metab       Date:  2021-05-10

3.  Orodental findings in postaxial acrofacial dysostosis.

Authors:  Aadithya B Urs; Priya Kumar; Kalpana Nunia
Journal:  J Oral Maxillofac Pathol       Date:  2014-01

4.  Dihydro-orotate dehydrogenase is physically associated with the respiratory complex and its loss leads to mitochondrial dysfunction.

Authors:  JingXian Fang; Takeshi Uchiumi; Mikako Yagi; Shinya Matsumoto; Rie Amamoto; Shinya Takazaki; Haruyoshi Yamaza; Kazuaki Nonaka; Dongchon Kang
Journal:  Biosci Rep       Date:  2013-02-05       Impact factor: 3.840

5.  Protein instability and functional defects caused by mutations of dihydro-orotate dehydrogenase in Miller syndrome patients.

Authors:  JingXian Fang; Takeshi Uchiumi; Mikako Yagi; Shinya Matsumoto; Rie Amamoto; Toshiro Saito; Shinya Takazaki; Tomotake Kanki; Haruyoshi Yamaza; Kazuaki Nonaka; Dongchon Kang
Journal:  Biosci Rep       Date:  2012-12       Impact factor: 3.840

6.  Using variant databases for variant prioritization and to detect erroneous genotype-phenotype associations.

Authors:  Bart J G Broeckx; Luc Peelman; Jimmy H Saunders; Dieter Deforce; Lieven Clement
Journal:  BMC Bioinformatics       Date:  2017-12-01       Impact factor: 3.169

7.  Broad-spectrum next-generation sequencing-based diagnosis of a case of Nager syndrome.

Authors:  Jue Zhao; Liwei Yang
Journal:  J Clin Lab Anal       Date:  2020-06-14       Impact factor: 2.352
  7 in total

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