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U Zafar

Showing results (31-40 of 45) with videos related to

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European Journal of Clinical Investigation|February 19, 2008
Ovariectomy increases vascular calcification via the OPG/RANKL cytokine signalling pathwayB G Choi, G Vilahur, L Cardoso, et al.
Journal of Thrombosis and Haemostasis : JTH|November 10, 2012
Platelet function normalization after a prasugrel loading-dose: time-dependent effect of platelet supplementationM U Zafar, C Santos-Gallego, D A Vorchheimer, et al.
Molecular Vision|January 5, 2011
Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8pNamerah Sabir, S Amer Riazuddin, Haiba Kaul, et al.
The British Journal of Ophthalmology|March 31, 2011
Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani familiesShagufta Naz, Shahbaz Ali, S Amer Riazuddin, et al.
Molecular Vision|December 24, 2010
Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3qNamerah Sabir, S Amer Riazuddin, Tariq Butt, et al.
Human Genetics|August 11, 2007
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3Quratul Ain, Sabiha Nazli, Saima Riazuddin, et al.
Molecular Vision|April 21, 2010
Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1Afshan Yasmeen, S Amer Riazuddin, Haiba Kaul, et al.
Frontiers in Oncology|October 24, 2022
Outcomes with mismatched unrelated donor allogeneic hematopoietic stem cell transplantation in adults: A systematic review and meta-analysisMuhammad Umair Mushtaq, Moazzam Shahzad, Ezza Tariq, et al.
American Journal of Human Genetics|August 4, 2009
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndromeSaima Riazuddin, Saima Anwar, Martin Fischer, et al.
Frontiers in Immunology|October 20, 2022
Impact of natural killer cells on outcomes after allogeneic hematopoietic stem cell transplantation: A systematic review and meta-analysisMuhammad Umair Mushtaq, Moazzam Shahzad, Amna Y Shah, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
European Journal of Clinical Investigation|February 19, 2008
Ovariectomy increases vascular calcification via the OPG/RANKL cytokine signalling pathwayB G Choi, G Vilahur, L Cardoso, et al.
Journal of Thrombosis and Haemostasis : JTH|November 10, 2012
Platelet function normalization after a prasugrel loading-dose: time-dependent effect of platelet supplementationM U Zafar, C Santos-Gallego, D A Vorchheimer, et al.
Molecular Vision|January 5, 2011
Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8pNamerah Sabir, S Amer Riazuddin, Haiba Kaul, et al.
The British Journal of Ophthalmology|March 31, 2011
Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani familiesShagufta Naz, Shahbaz Ali, S Amer Riazuddin, et al.
Molecular Vision|December 24, 2010
Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3qNamerah Sabir, S Amer Riazuddin, Tariq Butt, et al.
Human Genetics|August 11, 2007
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3Quratul Ain, Sabiha Nazli, Saima Riazuddin, et al.
Molecular Vision|April 21, 2010
Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1Afshan Yasmeen, S Amer Riazuddin, Haiba Kaul, et al.
Frontiers in Oncology|October 24, 2022
Outcomes with mismatched unrelated donor allogeneic hematopoietic stem cell transplantation in adults: A systematic review and meta-analysisMuhammad Umair Mushtaq, Moazzam Shahzad, Ezza Tariq, et al.
American Journal of Human Genetics|August 4, 2009
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndromeSaima Riazuddin, Saima Anwar, Martin Fischer, et al.
Frontiers in Immunology|October 20, 2022
Impact of natural killer cells on outcomes after allogeneic hematopoietic stem cell transplantation: A systematic review and meta-analysisMuhammad Umair Mushtaq, Moazzam Shahzad, Amna Y Shah, et al.
Pageof 5