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Blood
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July 15, 1997
Jak1 plays an essential role for receptor phosphorylation and Stat activation in response to granulocyte colony-stimulating factor
K Shimoda, J Feng, H Murakami, et al.
The Journal of Biological Chemistry
|
October 27, 1995
Modulation of cardiac Na+ channel expression in Xenopus oocytes by beta 1 subunits
Y Qu, L L Isom, R E Westenbroek, et al.
Updates in Surgery
|
March 3, 2022
Feasibility and usability of a regional hub model for colorectal cancer services during the COVID-19 pandemic
Filipe Carvalho, Ailín C Rogers, Tou-Pin Chang, et al.
The Journal of Biological Chemistry
|
September 28, 2000
Roles of two homotetrameric kinesins in sea urchin embryonic cell division
K K Chui, G C Rogers, A M Kashina, et al.
The Journal of Cell Biology
|
August 10, 2000
A kinesin-related protein, KRP(180), positions prometaphase spindle poles during early sea urchin embryonic cell division
G C Rogers, K K Chui, E W Lee, et al.
Molecular Biology of the Cell
|
September 27, 2018
Asterless is a Polo-like kinase 4 substrate that both activates and inhibits kinase activity depending on its phosphorylation state
Cody J Boese, Jonathan Nye, Daniel W Buster, et al.
Molecular Biology of the Cell
|
May 10, 2023
Polo-like kinase 4 homodimerization and condensate formation regulate its own protein levels but are not required for centriole assembly
John M Ryniawec, Daniel W Buster, Lauren K Slevin, et al.
Journal of Medical Genetics
|
August 14, 2008
Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia
F E Abidi, L Holloway, C A Moore, et al.
Pediatric Research
|
December 1, 1989
Blood flow during cardiopulmonary resuscitation with simultaneous compression and ventilation in infant pigs
I D Berkowitz, T Chantarojanasiri, R C Koehler, et al.
Clinical Genetics
|
August 26, 2010
Germline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndrome
K J Champion, C Bunag, A L Estep, et al.
Page
of 136
Search research articles
Search
Showing results (1031-1040 of 1,360) with videos related to
Sort By:
Page
of 136
Blood
|
July 15, 1997
Jak1 plays an essential role for receptor phosphorylation and Stat activation in response to granulocyte colony-stimulating factor
K Shimoda, J Feng, H Murakami, et al.
The Journal of Biological Chemistry
|
October 27, 1995
Modulation of cardiac Na+ channel expression in Xenopus oocytes by beta 1 subunits
Y Qu, L L Isom, R E Westenbroek, et al.
Updates in Surgery
|
March 3, 2022
Feasibility and usability of a regional hub model for colorectal cancer services during the COVID-19 pandemic
Filipe Carvalho, Ailín C Rogers, Tou-Pin Chang, et al.
The Journal of Biological Chemistry
|
September 28, 2000
Roles of two homotetrameric kinesins in sea urchin embryonic cell division
K K Chui, G C Rogers, A M Kashina, et al.
The Journal of Cell Biology
|
August 10, 2000
A kinesin-related protein, KRP(180), positions prometaphase spindle poles during early sea urchin embryonic cell division
G C Rogers, K K Chui, E W Lee, et al.
Molecular Biology of the Cell
|
September 27, 2018
Asterless is a Polo-like kinase 4 substrate that both activates and inhibits kinase activity depending on its phosphorylation state
Cody J Boese, Jonathan Nye, Daniel W Buster, et al.
Molecular Biology of the Cell
|
May 10, 2023
Polo-like kinase 4 homodimerization and condensate formation regulate its own protein levels but are not required for centriole assembly
John M Ryniawec, Daniel W Buster, Lauren K Slevin, et al.
Journal of Medical Genetics
|
August 14, 2008
Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia
F E Abidi, L Holloway, C A Moore, et al.
Pediatric Research
|
December 1, 1989
Blood flow during cardiopulmonary resuscitation with simultaneous compression and ventilation in infant pigs
I D Berkowitz, T Chantarojanasiri, R C Koehler, et al.
Clinical Genetics
|
August 26, 2010
Germline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndrome
K J Champion, C Bunag, A L Estep, et al.
Page
of 136