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Showing results (431-440 of 493) with videos related to

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Molecular and Cellular Biochemistry|July 9, 2024
Death associated protein like 1 acts as a novel tumor suppressor in melanoma by increasing the stability of P21 proteinXiaoyan Liu, Xiaojuan Hu, Meiyu Jing, et al.
Molecular Vision|May 2, 2020
Mutations in <i>FYCO1</i> identified in families with congenital cataractsHira Iqbal, Shahid Y Khan, Lin Zhou, et al.
Investigative Ophthalmology & Visual Science|August 1, 2006
Screening of the eight BBS genes in Tunisian families: no evidence of triallelismNizar Smaoui, Myriam Chaabouni, Yuri V Sergeev, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 12, 2011
Association of pathogenic mutations in TULP1 with retinitis pigmentosa in consanguineous Pakistani familiesMuhammad Iqbal, Muhammad Asif Naeem, S Amer Riazuddin, et al.
The Journal of the American Osteopathic Association|December 29, 2006
Multiple aortocoronary bypass saphenous vein graft aneurysms in a 77-year-old manAnne-Marie Moukala-Cadet, Stephen J Mitrosky, Glenn D Miller, et al.
Nature Communications|November 30, 2016
Direct visualization of a Fe(IV)-OH intermediate in a heme enzymeHanna Kwon, Jaswir Basran, Cecilia M Casadei, 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.
Molecular Vision|June 17, 2016
Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial casesFiroz Kabir, Inayat Ullah, Shahbaz Ali, 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|July 22, 2016
Pathogenic mutations in TULP1 responsible for retinitis pigmentosa identified in consanguineous familial casesInayat Ullah, Firoz Kabir, Muhammad Iqbal, et al.
Pageof 50

Showing results (431-440 of 493) with videos related to

Sort By:
Pageof 50
Molecular and Cellular Biochemistry|July 9, 2024
Death associated protein like 1 acts as a novel tumor suppressor in melanoma by increasing the stability of P21 proteinXiaoyan Liu, Xiaojuan Hu, Meiyu Jing, et al.
Molecular Vision|May 2, 2020
Mutations in <i>FYCO1</i> identified in families with congenital cataractsHira Iqbal, Shahid Y Khan, Lin Zhou, et al.
Investigative Ophthalmology & Visual Science|August 1, 2006
Screening of the eight BBS genes in Tunisian families: no evidence of triallelismNizar Smaoui, Myriam Chaabouni, Yuri V Sergeev, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 12, 2011
Association of pathogenic mutations in TULP1 with retinitis pigmentosa in consanguineous Pakistani familiesMuhammad Iqbal, Muhammad Asif Naeem, S Amer Riazuddin, et al.
The Journal of the American Osteopathic Association|December 29, 2006
Multiple aortocoronary bypass saphenous vein graft aneurysms in a 77-year-old manAnne-Marie Moukala-Cadet, Stephen J Mitrosky, Glenn D Miller, et al.
Nature Communications|November 30, 2016
Direct visualization of a Fe(IV)-OH intermediate in a heme enzymeHanna Kwon, Jaswir Basran, Cecilia M Casadei, 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.
Molecular Vision|June 17, 2016
Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial casesFiroz Kabir, Inayat Ullah, Shahbaz Ali, 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|July 22, 2016
Pathogenic mutations in TULP1 responsible for retinitis pigmentosa identified in consanguineous familial casesInayat Ullah, Firoz Kabir, Muhammad Iqbal, et al.
Pageof 50