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Xiang‐Qian Song

Observed names: XIANG-QIAN SONG, Xiang-Qian Song, Xiang-qian Song, Xiangqian Song
OpenAlex ID: A5110152885
Enzymes of Ketone Body Utilization in Human Tissues: Protein and Messenger RNA Levels of Succinyl-Coenzyme A (CoA):3-Ketoacid CoA Transferase and Mitochondrial and Cytosolic Acetoacetyl-CoA Thiolases
1997 · Toshiyuki Fukao, Xiang-Qian Song, et al. · Pediatric Research · 178
Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT): Cloning of the Human SCOT Gene, Tertiary Structural Modeling of the Human SCOT Monomer, and Characterization of Three Pathogenic Mutations
2000 · Toshiyuki Fukao, Grant A. Mitchell, et al. · Genomics · 60
Blood-induced bone loss in murine hemophilic arthropathy is prevented by blocking the iRhom2/ADAM17/TNF-α pathway
2018 · Coline Haxaire, Narine Hakobyan, et al. · Blood · 59
Liver-Specific Silencing of the Human Gene Encoding Succinyl-CoA: 3-Ketoacid CoA Transferase
2008 · Kenji E. Orii, Toshiyuki Fukao, et al. · The Tohoku Journal of Experimental Medicine · 49
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Mucopolysaccharidosis type II (Hunter disease): Identification and characterization of eight point mutations in the iduronate-2-sulfatase gene in Japanese patients
1995 · Kazuko Sukegawa, Shunji Tomatsu, et al. · Human Mutation · 41
Characterization of N93S, I312T, and A333P missense mutations in two Japanese families with mitochondrial acetoacetyl-CoA thiolase deficiency
1998 · Toshiyuki Fukao, Haruki Nakamura, et al. · Human Mutation · 39
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Functional conservation of HIV-1 Vpr and variability in a mother–child pair of long-term non-progressors
2002 · Yuqi Zhao, Mingzhong Chen, et al. · Virus Research · 33
Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: Two pathogenic mutations, V133E and C456F, in Japanese siblings
1998 · Xiang-Qian Song, Toshiyuki Fukao, et al. · Human Mutation · 27
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Hunter disease in a girl caused by R468Q mutation in the iduronate-2-sulfatase gene and skewed inactivation of the X chromosome carrying the normal allele
1997 · Kazuko Sukegawa, Xiang-Qian Song, et al. · Human Mutation · 27
Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): Development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency
1997 · Xiang-Qian Song, Toshiyuki Fukao, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 25
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Immunotitration Analysis of Cytosolic Acetoacetyl-Coenzyme A Thiolase Activity in Human Fibroblasts
1996 · Toshiyuki Fukao, Xiang-Qian Song, et al. · Pediatric Research · 23
A Novel Single-Base Substitution (380C>T) That Activates a 5-Base Downstream Cryptic Splice-Acceptor Site within Exon 5 in Almost All Transcripts in the Human Mitochondrial Acetoacetyl-CoA Thiolase Gene
2001 · Kozue Nakamura, Toshiyuki Fukao, et al. · Molecular Genetics and Metabolism · 22
Prenatal Diagnosis of Succinyl-coenzyme A:3-ketoacid Coenzyme a Transferase Deficiency
1996 · TOSHIYUKI FUKAO, XIANG-QIAN SONG, et al. · Prenatal Diagnosis · 22
Identification of three novel frameshift mutations (83delAT, 754insCT, and 435 + 1G to A) of mitochondrial acetoacetyl‐coenzyme A thiolase gene in two Swiss patients with CRM‐negative β‐ketothiolase deficiency
1997 · Toshiyuki Fukao, Xiang‐Qian Song, et al. · Human Mutation · 21
Molecular basis of very long chain acyl-CoA dehydrogenase deficiency in three Israeli patients: Identification of a complex mutant allele with P65L and K247Q mutations, the former being an exonic mutation causing exon 3 skipping
2000 · Hiroh Watanabe, Kenji E. Orii, et al. · Human Mutation · 20
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Two novel missense mutations in the ATP‐binding domain of the adrenoleukodystrophy gene: immunoblotting and immunocytological study of two patients
1997 · Atsushi Imamura, Yasuyuki Suzuki, et al. · Clinical Genetics · 15
Mitochondrial acetoacetyl-coenzyme a thiolase gene: A Novel 68-bp deletion involving 3′ splice site of intron 7, causing exon 8 skipping in a caucasian patient with β-ketothiolase deficiency
1995 · Toshiyuki Fukao, Xiang-Qian Song, et al. · Human Mutation · 14
Assignment of the Human Cytosolic Acetoacetyl-Coenzyme A Thiolase (ACAT2) Gene to Chromosome 6q25.3–q26
1996 · Mitsuo Masuno, Toshiyuki Fukao, et al. · Genomics · 11
Cyclothiazide: a subunit‐specific inhibitor of GABACreceptors
2008 · An Xie, Xiangqian Song, et al. · The Journal of Physiology · 10
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Prenatal Diagnosis of Adrenoleukodystrophy by Means of Mutation Analysis
1996 · ATSUSHI IMAMURA, YASUYUKI SUZUKI, et al. · Prenatal Diagnosis · 9
Mild form of beta‐ketothiolase deficiency (mitochondrial acetoacetyl‐CoA thiolase deficiency) in two Japanese siblings: identification of detectable residual activity and cross‐reactive material in EB‐transformed lymphocytes
1996 · Toshiyuki Fukao, Akihiko Kodama, et al. · Clinical Genetics · 8
Prenatal diagnosis in a family with mitochondrial acetoacetyl‐coenzyme a thiolase deficiency with the use of the polymerase chain reaction followed by the heteroduplex detection method
1995 · Toshiyuki Fukao, Akihiro Wakazono, et al. · Prenatal Diagnosis · 8
Ataxia-telangiectasia in the Japanese population: Identification of R1917X, W2491R, R2909G, IVS33+2T→A, and 7883del5, the latter two being relatively common mutations
1998 · Toshiyuki Fukao, Xiang-Qian Song, et al. · Human Mutation · 6
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Practical Assay Method of Cytosolic Acetoacetyl-CoA Thiolase by Rapid Release of Cytosolic Enzymes from Cultured Lymphocytes Using Digitonin.
1998 · Hiroshi Watanabe, Seiji Yamaguchi, et al. · The Tohoku Journal of Experimental Medicine · 2
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Biologic Response and Adverse Events To Stimate In Patients With Von Willebrand Disease
2013 · Xiangqian Song, Leonard A. Valentino, et al. · Blood
Works count: 25
Citation count: 729
H-index: 15
I10-index: 19
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