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Epilepsia
|
May 16, 2008
Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy
Ji-wen Wang, Hirokazu Kurahashi, Atsushi Ishii, et al.
Japanese Journal of Clinical Oncology
|
February 7, 2025
Clinicopathological background of local recurrence in high grade sarcoma of the extremity with preoperative chemotherapy: a supplementary analysis of JCOG0304
Satoshi Tsukushi, Kazuhiro Tanaka, Toshiyuki Kunisada, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 21, 2008
Rats harboring S284L Chrna4 mutation show attenuation of synaptic and extrasynaptic GABAergic transmission and exhibit the nocturnal frontal lobe epilepsy phenotype
Gang Zhu, Motohiro Okada, Shukuko Yoshida, et al.
Human Mutation
|
May 30, 2009
The phenotype and genotype experiment object model (PaGE-OM): a robust data structure for information related to DNA variation
Anthony J Brookes, Heikki Lehvaslaiho, Juha Muilu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 7, 2009
CKIepsilon/delta-dependent phosphorylation is a temperature-insensitive, period-determining process in the mammalian circadian clock
Yasushi Isojima, Masato Nakajima, Hideki Ukai, et al.
Atherosclerosis
|
January 8, 2011
Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations
Yoshiji Yamada, Tamotsu Nishida, Sahoko Ichihara, et al.
Plos One
|
December 17, 2009
RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans
Paola Sebastiani, Monty Montano, Annibale Puca, et al.
Human Mutation
|
March 24, 2009
Planning the human variome project: the Spain report
Jim Kaput, Richard G H Cotton, Lauren Hardman, et al.
Nature Genetics
|
April 21, 2009
The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line
, Harukazu Suzuki, Alistair R R Forrest, et al.
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of 8
Search research articles
Search
Showing results (71-80 of 79) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 79 results.
Epilepsia
|
May 16, 2008
Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy
Ji-wen Wang, Hirokazu Kurahashi, Atsushi Ishii, et al.
Japanese Journal of Clinical Oncology
|
February 7, 2025
Clinicopathological background of local recurrence in high grade sarcoma of the extremity with preoperative chemotherapy: a supplementary analysis of JCOG0304
Satoshi Tsukushi, Kazuhiro Tanaka, Toshiyuki Kunisada, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 21, 2008
Rats harboring S284L Chrna4 mutation show attenuation of synaptic and extrasynaptic GABAergic transmission and exhibit the nocturnal frontal lobe epilepsy phenotype
Gang Zhu, Motohiro Okada, Shukuko Yoshida, et al.
Human Mutation
|
May 30, 2009
The phenotype and genotype experiment object model (PaGE-OM): a robust data structure for information related to DNA variation
Anthony J Brookes, Heikki Lehvaslaiho, Juha Muilu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 7, 2009
CKIepsilon/delta-dependent phosphorylation is a temperature-insensitive, period-determining process in the mammalian circadian clock
Yasushi Isojima, Masato Nakajima, Hideki Ukai, et al.
Atherosclerosis
|
January 8, 2011
Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations
Yoshiji Yamada, Tamotsu Nishida, Sahoko Ichihara, et al.
Plos One
|
December 17, 2009
RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans
Paola Sebastiani, Monty Montano, Annibale Puca, et al.
Human Mutation
|
March 24, 2009
Planning the human variome project: the Spain report
Jim Kaput, Richard G H Cotton, Lauren Hardman, et al.
Nature Genetics
|
April 21, 2009
The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line
, Harukazu Suzuki, Alistair R R Forrest, et al.
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of 8