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Molecular and Cellular Biochemistry
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July 9, 2024
Death associated protein like 1 acts as a novel tumor suppressor in melanoma by increasing the stability of P21 protein
Xiaoyan Liu, Xiaojuan Hu, Meiyu Jing, et al.
Molecular Vision
|
May 2, 2020
Mutations in <i>FYCO1</i> identified in families with congenital cataracts
Hira 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 triallelism
Nizar 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 families
Muhammad 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 man
Anne-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 enzyme
Hanna 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 8p
Namerah 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 cases
Firoz 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 families
Shagufta 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 cases
Inayat Ullah, Firoz Kabir, Muhammad Iqbal, et al.
Page
of 50
Search research articles
Search
Showing results (431-440 of 493) with videos related to
Sort By:
Page
of 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 protein
Xiaoyan Liu, Xiaojuan Hu, Meiyu Jing, et al.
Molecular Vision
|
May 2, 2020
Mutations in <i>FYCO1</i> identified in families with congenital cataracts
Hira 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 triallelism
Nizar 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 families
Muhammad 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 man
Anne-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 enzyme
Hanna 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 8p
Namerah 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 cases
Firoz 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 families
Shagufta 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 cases
Inayat Ullah, Firoz Kabir, Muhammad Iqbal, et al.
Page
of 50