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Human Molecular Genetics
|
June 12, 2009
Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3
Rachaneekorn Tammachote, Cynthia J Hommerding, Rachel M Sinders, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
November 13, 2004
Polymorphisms of the interleukin-1beta gene affect the risk of myocardial infarction and ischemic stroke at young age and the response of mononuclear cells to stimulation in vitro
L Iacoviello, A Di Castelnuovo, M Gattone, et al.
Kidney International
|
May 24, 2007
A mouse model of autosomal recessive polycystic kidney disease with biliary duct and proximal tubule dilatation
J R Woollard, R Punyashtiti, S Richardson, et al.
Plos One
|
February 6, 2013
A telomerase immortalized human proximal tubule cell line with a truncation mutation (Q4004X) in polycystin-1
Brittney-Shea Herbert, Brenda R Grimes, Wei Min Xu, et al.
Giornale Italiano Di Cardiologia (2006)
|
October 1, 2010
[Cardiovascular epidemiologic observatory 2008-2011: preliminary results]
Diego Vanuzzo, Noce Cinzia Lo, Lorenza Pilotto, et al.
Journal of Thrombosis and Haemostasis : JTH
|
July 9, 2009
Tissue factor gene polymorphisms and haplotypes and the risk of ischemic vascular events: four studies and a meta-analysis
M DE Gaetano, G Quacquaruccio, A Pezzini, et al.
The Journal of Clinical Investigation
|
September 5, 2018
Loss of placental growth factor ameliorates maternal hypertension and preeclampsia in mice
Jacqueline G Parchem, Keizo Kanasaki, Megumi Kanasaki, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
February 9, 2008
Non-pharmacological control of plasma cholesterol levels
Andrea Poli, Franca Marangoni, Rodolfo Paoletti, et al.
Pharmacological Research
|
October 3, 2020
Is there a link between inorganic polyphosphate (polyP), mitochondria, and neurodegeneration?
Emily A Borden, Matthew Furey, Nicholas J Gattone, et al.
Nature Genetics
|
January 18, 2006
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
Ursula M Smith, Mark Consugar, Louise J Tee, et al.
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Search research articles
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Showing results (201-210 of 210) with videos related to
Sort By:
Page
of 21
You have reached the last page of results.
This site can display upto 210 results.
Human Molecular Genetics
|
June 12, 2009
Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3
Rachaneekorn Tammachote, Cynthia J Hommerding, Rachel M Sinders, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
November 13, 2004
Polymorphisms of the interleukin-1beta gene affect the risk of myocardial infarction and ischemic stroke at young age and the response of mononuclear cells to stimulation in vitro
L Iacoviello, A Di Castelnuovo, M Gattone, et al.
Kidney International
|
May 24, 2007
A mouse model of autosomal recessive polycystic kidney disease with biliary duct and proximal tubule dilatation
J R Woollard, R Punyashtiti, S Richardson, et al.
Plos One
|
February 6, 2013
A telomerase immortalized human proximal tubule cell line with a truncation mutation (Q4004X) in polycystin-1
Brittney-Shea Herbert, Brenda R Grimes, Wei Min Xu, et al.
Giornale Italiano Di Cardiologia (2006)
|
October 1, 2010
[Cardiovascular epidemiologic observatory 2008-2011: preliminary results]
Diego Vanuzzo, Noce Cinzia Lo, Lorenza Pilotto, et al.
Journal of Thrombosis and Haemostasis : JTH
|
July 9, 2009
Tissue factor gene polymorphisms and haplotypes and the risk of ischemic vascular events: four studies and a meta-analysis
M DE Gaetano, G Quacquaruccio, A Pezzini, et al.
The Journal of Clinical Investigation
|
September 5, 2018
Loss of placental growth factor ameliorates maternal hypertension and preeclampsia in mice
Jacqueline G Parchem, Keizo Kanasaki, Megumi Kanasaki, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
February 9, 2008
Non-pharmacological control of plasma cholesterol levels
Andrea Poli, Franca Marangoni, Rodolfo Paoletti, et al.
Pharmacological Research
|
October 3, 2020
Is there a link between inorganic polyphosphate (polyP), mitochondria, and neurodegeneration?
Emily A Borden, Matthew Furey, Nicholas J Gattone, et al.
Nature Genetics
|
January 18, 2006
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
Ursula M Smith, Mark Consugar, Louise J Tee, et al.
Page
of 21