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Leukemia Research
|
May 18, 2012
Casitas B-cell lymphoma mutation in childhood T-cell acute lymphoblastic leukemia
Yuka Saito, Yoko Aoki, Hideki Muramatsu, et al.
Journal of Medicinal Chemistry
|
December 30, 2020
Convenient Retinoid X Receptor Binding Assay Based on Fluorescence Change of the Antagonist NEt-C343
Kayo Yukawa-Takamatsu, Yifei Wang, Masaki Watanabe, et al.
Journal of Radiation Research
|
July 12, 2022
Abnormal sensation during total body irradiation: a prospective observational study
Masashi Mizumoto, Yoshiko Oshiro, Toshio Miyamoto, et al.
Journal of Anatomy
|
April 13, 2019
Revisiting the infracardiac bursa using multimodal methods: topographic anatomy for surgery of the esophagogastric junction
Tatsuro Nakamura, Hisashi Shinohara, Tomoaki Okada, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
April 9, 2019
Flavonoids differentially modulate liver X receptors activity-Structure-function relationship analysis
Allan Fouache, Nada Zabaiou, Cyrille De Joussineau, et al.
Cancer
|
June 30, 2017
Progressive hypofractionated carbon-ion radiotherapy for hepatocellular carcinoma: Combined analyses of 2 prospective trials
Goro Kasuya, Hirotoshi Kato, Shigeo Yasuda, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
October 3, 2022
Estimation of post-therapeutic liver reserve capacity using <sup>99m</sup>Tc-GSA scintigraphy prior to carbon-ion radiotherapy for liver tumors
Kana Yamazaki, Ryuichi Nishii, Yoichi Mizutani, et al.
European Journal of Clinical Pharmacology
|
March 15, 2019
Relationship between hemoglobin levels and vancomycin clearance in patients with sepsis
Masayuki Chuma, Makoto Makishima, Toru Imai, et al.
Cancer Research
|
December 17, 2008
250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies
Andrew J Dunbar, Lukasz P Gondek, Christine L O'Keefe, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain
Tomoko Makishima, Anne C Madeo, Carmen C Brewer, et al.
Page
of 74
Search research articles
Search
Showing results (581-590 of 737) with videos related to
Sort By:
Page
of 74
Leukemia Research
|
May 18, 2012
Casitas B-cell lymphoma mutation in childhood T-cell acute lymphoblastic leukemia
Yuka Saito, Yoko Aoki, Hideki Muramatsu, et al.
Journal of Medicinal Chemistry
|
December 30, 2020
Convenient Retinoid X Receptor Binding Assay Based on Fluorescence Change of the Antagonist NEt-C343
Kayo Yukawa-Takamatsu, Yifei Wang, Masaki Watanabe, et al.
Journal of Radiation Research
|
July 12, 2022
Abnormal sensation during total body irradiation: a prospective observational study
Masashi Mizumoto, Yoshiko Oshiro, Toshio Miyamoto, et al.
Journal of Anatomy
|
April 13, 2019
Revisiting the infracardiac bursa using multimodal methods: topographic anatomy for surgery of the esophagogastric junction
Tatsuro Nakamura, Hisashi Shinohara, Tomoaki Okada, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
April 9, 2019
Flavonoids differentially modulate liver X receptors activity-Structure-function relationship analysis
Allan Fouache, Nada Zabaiou, Cyrille De Joussineau, et al.
Cancer
|
June 30, 2017
Progressive hypofractionated carbon-ion radiotherapy for hepatocellular carcinoma: Combined analyses of 2 prospective trials
Goro Kasuya, Hirotoshi Kato, Shigeo Yasuda, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
October 3, 2022
Estimation of post-therapeutic liver reserve capacity using <sup>99m</sup>Tc-GSA scintigraphy prior to carbon-ion radiotherapy for liver tumors
Kana Yamazaki, Ryuichi Nishii, Yoichi Mizutani, et al.
European Journal of Clinical Pharmacology
|
March 15, 2019
Relationship between hemoglobin levels and vancomycin clearance in patients with sepsis
Masayuki Chuma, Makoto Makishima, Toru Imai, et al.
Cancer Research
|
December 17, 2008
250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies
Andrew J Dunbar, Lukasz P Gondek, Christine L O'Keefe, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain
Tomoko Makishima, Anne C Madeo, Carmen C Brewer, et al.
Page
of 74