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Pathology International
|
December 7, 2000
Correlation between morphological heterogeneity and genetic alteration within one tumor in adenocarcinomas of the lung
M Yamasaki, Y Takeshima, S Fujii, et al.
Neurology
|
February 20, 1999
A novel deletion of the dystrophin S-promoter region cosegregating with mental retardation
D H Chen, Y Takeshima, Y Ishikawa, et al.
Proceedings of the Association of American Physicians
|
July 1, 1996
A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation
S Y Patria, H Alimsardjono, H Nishio, et al.
Human Pathology
|
December 1, 2001
Heterogeneous genetic alterations in ovarian mucinous tumors: application and usefulness of laser capture microdissection
Y Takeshima, V J Amatya, Y Daimaru, et al.
Biochemical and Biophysical Research Communications
|
September 13, 1996
Induction of exon skipping of the dystrophin transcript in lymphoblastoid cells by transfecting an antisense oligodeoxynucleotide complementary to an exon recognition sequence
Z A Pramono, Y Takeshima, H Alimsardjono, et al.
Pathology International
|
December 7, 2000
Correlation between genetic alterations and histopathological subtypes in bronchiolo-alveolar carcinoma and atypical adenomatous hyperplasia of the lung
M Yamasaki, Y Takeshima, S Fujii, et al.
The Journal of Clinical Investigation
|
December 31, 1997
Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy
N Shiga, Y Takeshima, H Sakamoto, et al.
Journal of Neurology
|
May 9, 2003
Analysis of dystrophin mRNA from skeletal muscle but not from lymphocytes led to identification of a novel nonsense mutation in a carrier of Duchenne muscular dystrophy
T Ito, Y Takeshima, M Yagi, et al.
Japanese Journal of Cancer Research : Gann
|
February 1, 1996
p16/CDKN2 gene and p53 gene alterations in Japanese non-smoking female lung adenocarcinoma
Y Takeshima, T Nishisaka, R Kawano, et al.
Kyobu Geka. the Japanese Journal of Thoracic Surgery
|
June 20, 2006
[Intralobar pulmonary sequestration with high level of serum CEA; report of a case]
T Noriyuki, T Okumichi, A Kimura, et al.
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of 8
Search research articles
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Showing results (41-50 of 79) with videos related to
Sort By:
Page
of 8
Pathology International
|
December 7, 2000
Correlation between morphological heterogeneity and genetic alteration within one tumor in adenocarcinomas of the lung
M Yamasaki, Y Takeshima, S Fujii, et al.
Neurology
|
February 20, 1999
A novel deletion of the dystrophin S-promoter region cosegregating with mental retardation
D H Chen, Y Takeshima, Y Ishikawa, et al.
Proceedings of the Association of American Physicians
|
July 1, 1996
A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation
S Y Patria, H Alimsardjono, H Nishio, et al.
Human Pathology
|
December 1, 2001
Heterogeneous genetic alterations in ovarian mucinous tumors: application and usefulness of laser capture microdissection
Y Takeshima, V J Amatya, Y Daimaru, et al.
Biochemical and Biophysical Research Communications
|
September 13, 1996
Induction of exon skipping of the dystrophin transcript in lymphoblastoid cells by transfecting an antisense oligodeoxynucleotide complementary to an exon recognition sequence
Z A Pramono, Y Takeshima, H Alimsardjono, et al.
Pathology International
|
December 7, 2000
Correlation between genetic alterations and histopathological subtypes in bronchiolo-alveolar carcinoma and atypical adenomatous hyperplasia of the lung
M Yamasaki, Y Takeshima, S Fujii, et al.
The Journal of Clinical Investigation
|
December 31, 1997
Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy
N Shiga, Y Takeshima, H Sakamoto, et al.
Journal of Neurology
|
May 9, 2003
Analysis of dystrophin mRNA from skeletal muscle but not from lymphocytes led to identification of a novel nonsense mutation in a carrier of Duchenne muscular dystrophy
T Ito, Y Takeshima, M Yagi, et al.
Japanese Journal of Cancer Research : Gann
|
February 1, 1996
p16/CDKN2 gene and p53 gene alterations in Japanese non-smoking female lung adenocarcinoma
Y Takeshima, T Nishisaka, R Kawano, et al.
Kyobu Geka. the Japanese Journal of Thoracic Surgery
|
June 20, 2006
[Intralobar pulmonary sequestration with high level of serum CEA; report of a case]
T Noriyuki, T Okumichi, A Kimura, et al.
Page
of 8