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Showing results (151-160 of 278) with videos related to

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Biochemistry|April 2, 1991
Circular dichroism and magnetic circular dichroism of Azotobacter vinelandii ferredoxin IP J Stephens, G M Jensen, F J Devlin, et al.
Journal of Dental Research|November 6, 2009
Regression of post-orthodontic lesions by a remineralizing creamD L Bailey, G G Adams, C E Tsao, et al.
Ginecologia Y Obstetricia De Mexico|November 24, 2015
[Laparoscopic myomectomy and use of electromechanical morcellator: clinical results in a series of cases]Fred Morgan-Ortiz, Juan Manuel Soto-Pineda, Alejandro Castro-Ibarra, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|February 13, 2001
n-3 polyunsaturated fatty acid supplementation, monocyte adhesion molecule expression and pro-inflammatory mediators in Type 2 diabetes mellitusM J Sampson, I R Davies, J C Brown, et al.
Platelets|February 22, 2021
A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorderIbrahim Almazni, Pavel Chudakou, Alison Dawson-Meadows, et al.
Psychological Medicine|October 1, 2005
The diagnostic interview for psychoses (DIP): development, reliability and applicationsD J Castle, A Jablensky, J J McGrath, et al.
Journal of Thrombosis and Haemostasis : JTH|October 6, 2020
Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression dataAbdullah O Khan, Rachel J Stapley, Jeremy A Pike, et al.
American Journal of Human Genetics|January 9, 2008
Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patientsJulie Vogt, Benjamin J Harrison, Hayley Spearman, et al.
Molecular Vision|May 23, 2009
Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataractEsther Meyer, Fatimah Rahman, Jessica Owens, et al.
European Journal of Medical Genetics|November 13, 2012
Acrocallosal syndrome: identification of a novel KIF7 mutation and evidence for oligogenic inheritanceDiana M Walsh, Stavit A Shalev, Michael A Simpson, et al.
Pageof 28

Showing results (151-160 of 278) with videos related to

Sort By:
Pageof 28
Biochemistry|April 2, 1991
Circular dichroism and magnetic circular dichroism of Azotobacter vinelandii ferredoxin IP J Stephens, G M Jensen, F J Devlin, et al.
Journal of Dental Research|November 6, 2009
Regression of post-orthodontic lesions by a remineralizing creamD L Bailey, G G Adams, C E Tsao, et al.
Ginecologia Y Obstetricia De Mexico|November 24, 2015
[Laparoscopic myomectomy and use of electromechanical morcellator: clinical results in a series of cases]Fred Morgan-Ortiz, Juan Manuel Soto-Pineda, Alejandro Castro-Ibarra, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|February 13, 2001
n-3 polyunsaturated fatty acid supplementation, monocyte adhesion molecule expression and pro-inflammatory mediators in Type 2 diabetes mellitusM J Sampson, I R Davies, J C Brown, et al.
Platelets|February 22, 2021
A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorderIbrahim Almazni, Pavel Chudakou, Alison Dawson-Meadows, et al.
Psychological Medicine|October 1, 2005
The diagnostic interview for psychoses (DIP): development, reliability and applicationsD J Castle, A Jablensky, J J McGrath, et al.
Journal of Thrombosis and Haemostasis : JTH|October 6, 2020
Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression dataAbdullah O Khan, Rachel J Stapley, Jeremy A Pike, et al.
American Journal of Human Genetics|January 9, 2008
Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patientsJulie Vogt, Benjamin J Harrison, Hayley Spearman, et al.
Molecular Vision|May 23, 2009
Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataractEsther Meyer, Fatimah Rahman, Jessica Owens, et al.
European Journal of Medical Genetics|November 13, 2012
Acrocallosal syndrome: identification of a novel KIF7 mutation and evidence for oligogenic inheritanceDiana M Walsh, Stavit A Shalev, Michael A Simpson, et al.
Pageof 28