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Journal of Cell Science
|
April 13, 2006
Dynamic microtubules regulate the local concentration of E-cadherin at cell-cell contacts
Samantha J Stehbens, Andrew D Paterson, Matthew S Crampton, et al.
Plos One
|
July 26, 2023
Genetics of cannabis use in opioid use disorder: A genome-wide association and polygenic risk score study
Alannah Hillmer, Caroul Chawar, Amel Lamri, et al.
Plos One
|
March 17, 2017
The duplication mutation of Quebec platelet disorder dysregulates PLAU, but not C10orf55, selectively increasing production of normal PLAU transcripts by megakaryocytes but not granulocytes
Catherine P M Hayward, Minggao Liang, Subia Tasneem, et al.
BMJ (Clinical Research Ed.)
|
February 22, 1992
Cost benefits of low dose subcutaneous erythropoietin in patients with anaemia of end stage renal disease
M E Stevens, G P Summerfield, A A Hall, et al.
The Journal of Urology
|
June 19, 2012
Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort
James M Hotaling, Daryl R Waggott, Jack Goldberg, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
December 25, 2008
Mammographic density: a heritable risk factor for breast cancer
Norman F Boyd, Lisa J Martin, Johanna M Rommens, et al.
Kidney International
|
May 9, 1998
A novel frameshift mutation induced by an adenosine insertion in the polycystic kidney disease 2 (PKD2) gene
Y Pei, K Wang, M Kasenda, et al.
Bipolar Disorders
|
May 18, 2026
Genetic Linkage for Bipolar Disorder to the Distal Region of Chromosome 19q: A Large Family Whole Genome Sequencing Study
Albert H C Wong, Andrew D Paterson, Nicole M Roslin, et al.
Human Genetics
|
December 10, 2014
The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy
S Mohsen Hosseini, Andrew P Boright, Lei Sun, et al.
Clinical Genetics
|
February 1, 2005
A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13
S H E Zaidi, V Peltekova, S Meyer, et al.
Page
of 54
Search research articles
Search
Showing results (341-350 of 540) with videos related to
Sort By:
Page
of 54
Journal of Cell Science
|
April 13, 2006
Dynamic microtubules regulate the local concentration of E-cadherin at cell-cell contacts
Samantha J Stehbens, Andrew D Paterson, Matthew S Crampton, et al.
Plos One
|
July 26, 2023
Genetics of cannabis use in opioid use disorder: A genome-wide association and polygenic risk score study
Alannah Hillmer, Caroul Chawar, Amel Lamri, et al.
Plos One
|
March 17, 2017
The duplication mutation of Quebec platelet disorder dysregulates PLAU, but not C10orf55, selectively increasing production of normal PLAU transcripts by megakaryocytes but not granulocytes
Catherine P M Hayward, Minggao Liang, Subia Tasneem, et al.
BMJ (Clinical Research Ed.)
|
February 22, 1992
Cost benefits of low dose subcutaneous erythropoietin in patients with anaemia of end stage renal disease
M E Stevens, G P Summerfield, A A Hall, et al.
The Journal of Urology
|
June 19, 2012
Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort
James M Hotaling, Daryl R Waggott, Jack Goldberg, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
December 25, 2008
Mammographic density: a heritable risk factor for breast cancer
Norman F Boyd, Lisa J Martin, Johanna M Rommens, et al.
Kidney International
|
May 9, 1998
A novel frameshift mutation induced by an adenosine insertion in the polycystic kidney disease 2 (PKD2) gene
Y Pei, K Wang, M Kasenda, et al.
Bipolar Disorders
|
May 18, 2026
Genetic Linkage for Bipolar Disorder to the Distal Region of Chromosome 19q: A Large Family Whole Genome Sequencing Study
Albert H C Wong, Andrew D Paterson, Nicole M Roslin, et al.
Human Genetics
|
December 10, 2014
The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy
S Mohsen Hosseini, Andrew P Boright, Lei Sun, et al.
Clinical Genetics
|
February 1, 2005
A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13
S H E Zaidi, V Peltekova, S Meyer, et al.
Page
of 54