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D PATERSON

Showing results (341-350 of 540) with videos related to

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Journal of Cell Science|April 13, 2006
Dynamic microtubules regulate the local concentration of E-cadherin at cell-cell contactsSamantha 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 studyAlannah 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 granulocytesCatherine 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 diseaseM 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 cohortJames 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 cancerNorman 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) geneY 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 StudyAlbert 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 retinopathyS 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 20q13S H E Zaidi, V Peltekova, S Meyer, et al.
Pageof 54

Showing results (341-350 of 540) with videos related to

Sort By:
Pageof 54
Journal of Cell Science|April 13, 2006
Dynamic microtubules regulate the local concentration of E-cadherin at cell-cell contactsSamantha 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 studyAlannah 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 granulocytesCatherine 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 diseaseM 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 cohortJames 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 cancerNorman 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) geneY 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 StudyAlbert 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 retinopathyS 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 20q13S H E Zaidi, V Peltekova, S Meyer, et al.
Pageof 54