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Associations between bacterial communities of house dust and infant gut
Konya, T., Koster, B., Maughan, H., Escobar, M., Azad, M.B., Guttman, D.S., Sears, M.R., Becker, A.B., Brook, J.R., Takaro, T.K., Kozyrskyj, A.L., Scott, J.A.
Published in Environmental research (01.05.2014)
Published in Environmental research (01.05.2014)
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Ruthenium Ion-Catalyzed Oxidation of Shenfu Coal and Its Residues
Huang, Yao-Guo, Zong, Zhi-Min, Yao, Zi-Shuo, Zheng, Yu-Xuan, Mou, Jie, Liu, Guang-Feng, Cao, Jin-Pei, Ding, Ming-Jie, Cai, Ke-Ying, Wang, Feng, Zhao, Wei, Xia, Zhi-Lin, Wu, Lin, Wei, Xian-Yong
Published in Energy & fuels (01.05.2008)
Published in Energy & fuels (01.05.2008)
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Leber’s hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation
Liang, Min, Guan, Minqiang, Zhao, Fuxing, Zhou, Xiangtian, Yuan, Meixia, Tong, Yi, Yang, Li, Wei, Qi-Ping, Sun, Yan-Hong, Lu, Fan, Qu, Jia, Guan, Min-Xin
Published in Biochemical and biophysical research communications (05.06.2009)
Published in Biochemical and biophysical research communications (05.06.2009)
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Leber’s hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation
Zhao, Fuxin, Guan, Minqiang, Zhou, Xiangtian, Yuan, Meixia, Liang, Ming, Liu, Qi, Liu, Yan, Zhang, Yongmei, Yang, Li, Tong, Yi, Wei, Qi-Ping, Sun, Yan-Hong, Qu, Jia, Guan, Min-Xin
Published in Biochemical and biophysical research communications (20.11.2009)
Published in Biochemical and biophysical research communications (20.11.2009)
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Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss
Yuan, Huijun, Chen, Jing, Liu, Xin, Cheng, Jing, Wang, Xinjian, Yang, Li, Yang, Shuzhi, Cao, Juyang, Kang, Dongyang, Dai, Pu, Zhai, Suoqiang, Han, Dongyi, Young, Wie-Yen, Guan, Min-Xin
Published in Biochemical and biophysical research communications (12.10.2007)
Published in Biochemical and biophysical research communications (12.10.2007)
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Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity
Xing, Guangqian, Chen, Zhibin, Wei, Qinjun, Tian, Huiqin, Li, Xiaolu, Zhou, Aidong, Bu, Xingkuan, Cao, Xin
Published in Biochemical and biophysical research communications (11.08.2006)
Published in Biochemical and biophysical research communications (11.08.2006)
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Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation
Wang, Qiuju, Li, Qing-Zhong, Han, Dongyi, Zhao, Yali, Zhao, Lidong, Qian, Yaping, Yuan, Hu, Li, Ronghua, Zhai, Suoqiang, Young, Wie-Yen, Guan, Min-Xin
Published in Biochemical and biophysical research communications (10.02.2006)
Published in Biochemical and biophysical research communications (10.02.2006)
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Morphological and molecular characterization of fungal pathogen, Magnaphorthe oryzae
Hasan, Nor’Aishah, Rafii, Mohd Y., Rahim, Harun A., Ali, Nusaibah Syd, Mazlan, Norida, Abdullah, Shamsiah
Published in AIP conference proceedings (01.02.2016)
Published in AIP conference proceedings (01.02.2016)
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Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNA{sup Ser(UCN)} genes in two Chinese families
Zhu Yi, Liao Zhisu, Li Zhiyuan, Chen Jianfu, Qian Yaping, Tang Xiaowen, Wang Jindan, Yang Li, Li Ronghua, Ji Jinzhang, Choo, Daniel I., Lu Jianxin, Guan Minxin
Published in Biochemical and biophysical research communications (14.04.2006)
Published in Biochemical and biophysical research communications (14.04.2006)
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Leber’s hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families
Zhou, Xiangtian, Wei, Qiping, Yang, Li, Tong, Yi, Zhao, Fuxin, Lu, Chunjie, Qian, Yaping, Sun, Yanghong, Lu, Fan, Qu, Jia, Guan, Min-Xin
Published in Biochemical and biophysical research communications (03.02.2006)
Published in Biochemical and biophysical research communications (03.02.2006)
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The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber’s hereditary optic neuropathy and hearing loss
Wei, Qi-Ping, Zhou, Xiangtian, Yang, Li, Sun, Yan-Hong, Zhou, Jian, Li, Guang, Jiang, Robert, Lu, Fan, Qu, Jia, Guan, Min-Xin
Published in Biochemical and biophysical research communications (15.06.2007)
Published in Biochemical and biophysical research communications (15.06.2007)
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FMS Mutations in Myelodysplastic, Leukemic, and Normal Subjects
Ridge, Susan A., Worwood, Mark, Oscier, David, Jacobs, Allan, Padua, Rose Ann
Published in Proceedings of the National Academy of Sciences - PNAS (01.02.1990)
Published in Proceedings of the National Academy of Sciences - PNAS (01.02.1990)
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Association between a Specific Apolipoprotein B Mutation and Familial Defective Apolipoprotein B-100
Soria, Luis F., Ludwig, Erwin H., Howard R. G. Clarke, Vega, Gloria L., Grundy, Scott M., McCarthy, Brian J.
Published in Proceedings of the National Academy of Sciences - PNAS (01.01.1989)
Published in Proceedings of the National Academy of Sciences - PNAS (01.01.1989)
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Molecular Cloning and Construction of the Coding Region for Human Acetylcholinesterase Reveals a G + C-Rich Attenuating Structure
Soreq, Hermona, Ben-Aziz, Revital, Prody, Catherine A., Seidman, Shlomo, Gnatt, Averell, Neville, Lewis, Lieman-Hurwitz, Judith, lev-Lehman, Efrat, Ginzberg, Dalia, Lapidot-Lifson, Yaron, Zakut, Haim
Published in Proceedings of the National Academy of Sciences - PNAS (01.12.1990)
Published in Proceedings of the National Academy of Sciences - PNAS (01.12.1990)
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Sequence variation in the androgen receptor gene is not a common determinant of male sexual orientation
MACKE, J. P, NAN HU, HU, S, BAILEY, M, KING, V. L, BROWN, T, HAMER, D, NATHANS, J
Published in American journal of human genetics (01.10.1993)
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Published in American journal of human genetics (01.10.1993)
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Identification of the Structural Mutation Responsible for the Dibucaine-Resistant (Atypical) Variant Form of Human Serum Cholinesterase
McGuire, Mary C., Nogueira, Christine P., Bartels, Cynthia F., Lightstone, Harold, Hajra, Amitav, Abraham F. L. Van Der Spek, Lockridge, Oksana, La Du, Bert N.
Published in Proceedings of the National Academy of Sciences - PNAS (01.02.1989)
Published in Proceedings of the National Academy of Sciences - PNAS (01.02.1989)
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Mucopolysaccharidosis IV A: Molecular Cloning of the Human N-Acetylgalactosamine-6-sulfatase Gene (GALNS) and Analysis of the 5′-Flanking Region
Nakashima, Yoshihiro, Tomatsu, Shunji, Hori, Toshinori, Fukuda, Seiji, Sukegawa, Kazuko, Kondo, Naomi, Suzuki, Yasuyuki, Shimozawa, Nobuyuki, Orii, Tadao
Published in Genomics (San Diego, Calif.) (01.03.1994)
Published in Genomics (San Diego, Calif.) (01.03.1994)
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Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis
CALABRO, V, MASON, P. J, FILOSA, S, CIVITELLI, D, CITTADELLA, R, TAGARELLI, A, MARTINI, G, BRANCATI, C, LUZZATTO, L
Published in American journal of human genetics (01.03.1993)
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Published in American journal of human genetics (01.03.1993)
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