X Q Song - JoVE Visualize

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RSC Advances|May 13, 2022

Synergistic and simultaneous biosorption of phenanthrene and iodine from aqueous solutions by soil indigenous bacterial biomass as a low-cost biosorbentD Zhang, S G Lu, X Q Song, et al.

The Tohoku Journal of Experimental Medicine|June 2, 1998

Practical assay method of cytosolic acetoacetyl-CoA thiolase by rapid release of cytosolic enzymes from cultured lymphocytes using digitoninH Watanabe, S Yamaguchi, M Kimura, et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia|July 27, 2016

Haemarthrosis model in mice: BSS - Bleeding Severity Score assessment systemN Hakobyan, L A Valentino, L Cong, et al.

Human Mutation|January 1, 1995

Mucopolysaccharidosis type II (Hunter disease): identification and characterization of eight point mutations in the iduronate-2-sulfatase gene in Japanese patientsK Sukegawa, S Tomatsu, T Fukao, et al.

Water Science and Technology : a Journal of the International Association on Water Pollution Research|January 20, 2005

Nitrite accumulation by aeration controlled in sequencing batch reactors treating domestic wastewaterY Z Peng, Y Chen, C Y Peng, et al.

Prenatal Diagnosis|May 1, 1996

Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiencyT Fukao, X Q Song, H Watanabe, et al.

Biochemical and Biophysical Research Communications|January 28, 1994

Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophyA Uchiyama, Y Suzuki, X Q Song, et al.

Journal of Inherited Metabolic Disease|March 21, 1998

Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease)K Isogai, K Sukegawa, S Tomatsu, et al.

Human Mutation|July 22, 1998

Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: two pathogenic mutations, V133E and C456F, in Japanese siblingsX Q Song, T Fukao, H Watanabe, et al.

European Review for Medical and Pharmacological Sciences|February 7, 2017

High expression of KIF14 is associated with poor prognosis in patients with epithelial ovarian cancerH-L Qiu, S-Z Deng, C Li, et al.

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Showing results (11-20 of 48) with videos related to

Sort By:

Pageof 5

RSC Advances|May 13, 2022

Synergistic and simultaneous biosorption of phenanthrene and iodine from aqueous solutions by soil indigenous bacterial biomass as a low-cost biosorbentD Zhang, S G Lu, X Q Song, et al.

The Tohoku Journal of Experimental Medicine|June 2, 1998

Practical assay method of cytosolic acetoacetyl-CoA thiolase by rapid release of cytosolic enzymes from cultured lymphocytes using digitoninH Watanabe, S Yamaguchi, M Kimura, et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia|July 27, 2016

Haemarthrosis model in mice: BSS - Bleeding Severity Score assessment systemN Hakobyan, L A Valentino, L Cong, et al.

Human Mutation|January 1, 1995

Mucopolysaccharidosis type II (Hunter disease): identification and characterization of eight point mutations in the iduronate-2-sulfatase gene in Japanese patientsK Sukegawa, S Tomatsu, T Fukao, et al.

Water Science and Technology : a Journal of the International Association on Water Pollution Research|January 20, 2005

Nitrite accumulation by aeration controlled in sequencing batch reactors treating domestic wastewaterY Z Peng, Y Chen, C Y Peng, et al.

Prenatal Diagnosis|May 1, 1996

Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiencyT Fukao, X Q Song, H Watanabe, et al.

Biochemical and Biophysical Research Communications|January 28, 1994

Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophyA Uchiyama, Y Suzuki, X Q Song, et al.

Journal of Inherited Metabolic Disease|March 21, 1998

Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease)K Isogai, K Sukegawa, S Tomatsu, et al.

Human Mutation|July 22, 1998

Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: two pathogenic mutations, V133E and C456F, in Japanese siblingsX Q Song, T Fukao, H Watanabe, et al.

European Review for Medical and Pharmacological Sciences|February 7, 2017

High expression of KIF14 is associated with poor prognosis in patients with epithelial ovarian cancerH-L Qiu, S-Z Deng, C Li, et al.

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