|
1
|
Quantification of lysophosphatidylcholines and phosphatidylcholines using liquid chromatography-tandem mass spectrometry in neonatal serum.
|
J Chromatogr B Analyt Technol Biomed Life Sci
|
2006
|
1.02
|
|
2
|
Mutation analysis of the ornithine transcarbamylase (OTC) gene in five Japanese OTC deficiency patients revealed two known and three novel mutations including a deep intronic mutation.
|
Kobe J Med Sci
|
2007
|
0.96
|
|
3
|
Wide ranges of serum myostatin concentrations in Duchenne muscular dystrophy patients.
|
Clin Chim Acta
|
2008
|
0.82
|
|
4
|
Co-occurrence of mutations in both dystrophin- and androgen-receptor genes is a novel cause of female Duchenne muscular dystrophy.
|
Hum Genet
|
2006
|
0.81
|
|
5
|
HnRNP C1/C2 may regulate exon 7 splicing in the spinal muscular atrophy gene SMN1.
|
Kobe J Med Sci
|
2009
|
0.80
|
|
6
|
Changes in regional cerebral blood volume in frontal cortex during mental work with and without caffeine intake: functional monitoring using near-infrared spectroscopy.
|
J Biomed Opt
|
2004
|
0.79
|
|
7
|
Two novel missense mutations in the myostatin gene identified in Japanese patients with Duchenne muscular dystrophy.
|
BMC Med Genet
|
2007
|
0.79
|
|
8
|
Identification of N-acetyl Proline-Glycine-Proline (acPGP) in human serum of adults and newborns by liquid chromatography-tandem mass spectrometry.
|
Clin Chim Acta
|
2009
|
0.78
|
|
9
|
Blood lysophosphatidylcholine (LPC) levels and characteristic molecular species in neonates: prolonged low blood LPC levels in very low birth weight infants.
|
Pediatr Res
|
2007
|
0.76
|
|
10
|
Evaluation of mutation effects on UGT1A1 activity toward 17beta-estradiol using liquid chromatography-tandem mass spectrometry.
|
J Chromatogr B Analyt Technol Biomed Life Sci
|
2006
|
0.75
|