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Journal of Inherited Metabolic Disease
|
January 1, 1992
Isolation of cDNA sequences around the chromosomal breakpoint in a female with Lowe syndrome by direct screening of cDNA libraries with yeast artificial chromosomes
I Okabe, O Attree, L C Bailey, et al.
The Journal of Biological Chemistry
|
April 10, 1999
Proliferative defect and embryonic lethality in mice homozygous for a deletion in the p110alpha subunit of phosphoinositide 3-kinase
L Bi, I Okabe, D J Bernard, et al.
Diabetologia
|
April 25, 2001
Splice site mutation in the hepatocyte nuclear factor-1 beta gene, IVS2nt + 1G > A, associated with maturity-onset diabetes of the young, renal dysplasia and bicornuate uterus
N Iwasaki, I Okabe, M Y Momoi, et al.
Pediatric Neurology
|
January 1, 1988
Does CSF copper level in Wilson disease reflect copper accumulation in the brain?
H Kodama, I Okabe, M Yanagisawa, et al.
Nihon Geka Gakkai Zasshi
|
September 1, 1991
[Experience of multimodal therapy for advanced neuroblastoma]
M Iwata, I Okabe, T Koshinaga, et al.
Lancet (London, England)
|
January 23, 1988
Chromosomes and screening for neuroblastoma
Y Kaneko, N Maseki, M Sakurai, et al.
Cancer Research
|
March 1, 1989
Frequent loss of heterozygosity on chromosome 14q in neuroblastoma
T Suzuki, J Yokota, H Mugishima, et al.
Progress in Clinical and Biological Research
|
January 1, 1991
Loss of heterozygosity on chromosome 14 in neuroblastoma
T Suzuki, H Mugishima, T Fujisawa, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
December 1, 1990
Current urinary mass screening for catecholamine metabolites at 6 months of age may be detecting only a small portion of high-risk neuroblastomas: a chromosome and N-myc amplification study
Y Kaneko, N Kanda, N Maseki, et al.
Nippon Ganka Gakkai Zasshi
|
March 1, 1995
[Hypotonous maculopathy following trabeculectomy with mitomycin C]
H Suemori-Matsushita, I Okabe, T Yamamoto, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 64) with videos related to
Sort By:
Page
of 7
Journal of Inherited Metabolic Disease
|
January 1, 1992
Isolation of cDNA sequences around the chromosomal breakpoint in a female with Lowe syndrome by direct screening of cDNA libraries with yeast artificial chromosomes
I Okabe, O Attree, L C Bailey, et al.
The Journal of Biological Chemistry
|
April 10, 1999
Proliferative defect and embryonic lethality in mice homozygous for a deletion in the p110alpha subunit of phosphoinositide 3-kinase
L Bi, I Okabe, D J Bernard, et al.
Diabetologia
|
April 25, 2001
Splice site mutation in the hepatocyte nuclear factor-1 beta gene, IVS2nt + 1G > A, associated with maturity-onset diabetes of the young, renal dysplasia and bicornuate uterus
N Iwasaki, I Okabe, M Y Momoi, et al.
Pediatric Neurology
|
January 1, 1988
Does CSF copper level in Wilson disease reflect copper accumulation in the brain?
H Kodama, I Okabe, M Yanagisawa, et al.
Nihon Geka Gakkai Zasshi
|
September 1, 1991
[Experience of multimodal therapy for advanced neuroblastoma]
M Iwata, I Okabe, T Koshinaga, et al.
Lancet (London, England)
|
January 23, 1988
Chromosomes and screening for neuroblastoma
Y Kaneko, N Maseki, M Sakurai, et al.
Cancer Research
|
March 1, 1989
Frequent loss of heterozygosity on chromosome 14q in neuroblastoma
T Suzuki, J Yokota, H Mugishima, et al.
Progress in Clinical and Biological Research
|
January 1, 1991
Loss of heterozygosity on chromosome 14 in neuroblastoma
T Suzuki, H Mugishima, T Fujisawa, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
December 1, 1990
Current urinary mass screening for catecholamine metabolites at 6 months of age may be detecting only a small portion of high-risk neuroblastomas: a chromosome and N-myc amplification study
Y Kaneko, N Kanda, N Maseki, et al.
Nippon Ganka Gakkai Zasshi
|
March 1, 1995
[Hypotonous maculopathy following trabeculectomy with mitomycin C]
H Suemori-Matsushita, I Okabe, T Yamamoto, et al.
Page
of 7