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Pediatric Research|July 4, 2008
Cardiac ion channel gene mutations in sudden infant death syndromeTesshu Otagiri, Kazuki Kijima, Motoki Osawa, et al.
Journal of Human Genetics|February 2, 2021
Y chromosome analysis for common surnames in the Japanese male populationEriko Ochiai, Motoki Osawa, Shiori Satoh, et al.
Electrophoresis|December 14, 2002
Complete mitochondrial DNA sequence of a tadpole shrimp (Triops cancriformis) and analysis of museum samplesKazuo Umetsu, Naruki Iwabuchi, Isao Yuasa, et al.
Journal of Human Genetics|October 26, 2019
Human short tandem repeat identification using a nanopore-based DNA sequencer: a pilot studyMinoru Asogawa, Ayumu Ohno, So Nakagawa, et al.
Pathology, Research and Practice|July 14, 2024
Layer-specific proteomic profiling of human normal heartYu Kakimoto, Atsushi Ueda, Yayoi Kimura, et al.
Human Genome Variation|October 21, 2020
Jervell and Lange-Nielsen syndrome with novel KCNQ1 and additional gene mutationsShinichi Matsuda, Yuko Ohnuki, Mayuri Okami, et al.
International Journal of Legal Medicine|March 1, 2005
Usefulness of serum mast cell-specific chymase levels for postmortem diagnosis of anaphylaxisHajime Nishio, Shinji Takai, Mizuo Miyazaki, et al.
FEBS Letters|November 19, 2003
A novel beta(1,6)-N-acetylglucosaminyltransferase V (GnT-VB)(1)Mika Kaneko, Gerardo Alvarez-Manilla, Maria Kamar, et al.
Biochemical and Biophysical Research Communications|September 19, 2006
Inhibition of tumor cell-induced platelet aggregation using a novel anti-podoplanin antibody reacting with its platelet-aggregation-stimulating domainYukinari Kato, Mika Kato Kaneko, Atsushi Kuno, et al.
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