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C P Pang

Showing results (71-80 of 132) with videos related to

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Human Mutation|February 6, 1998
Possible common mutations in the low density lipoprotein receptor gene in ChineseY T Mak, J Zhang, Y S Chan, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 9, 1998
Mutations in the low-density lipoprotein receptor gene in Chinese familial hypercholesterolemia patientsY T Mak, C P Pang, B Tomlinson, et al.
Eye (London, England)|July 12, 2008
A novel mutation in CRYBB2 responsible for inherited coronary cataractD Lou, J-P Tong, L-Y Zhang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's diseaseC P Pang, J Zhang, J Woo, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
An unusual case of multiple carboxylase deficiency presenting as generalized pustular psoriasis in a Chinese boyL K Law, C Y Lau, C P Pang, et al.
The Biochemical Journal|September 15, 1984
Stereochemistry of the incorporation of valine methyl groups into methylene groups in cephalosporin CC P Pang, R L White, E P Abraham, et al.
Investigative Ophthalmology & Visual Science|May 8, 2000
Truncations in the TIGR gene in individuals with and without primary open-angle glaucomaD S Lam, Y F Leung, J K Chua, et al.
The British Journal of Ophthalmology|August 25, 2001
Rhodopsin mutations in Chinese patients with retinitis pigmentosaW M Chan, K Y Yeung, C P Pang, et al.
Eye (London, England)|March 15, 2006
An in vitro study on the compatibility and concentrations of combinations of vancomycin, amikacin, and dexamethasone in human vitreousM Hui, A K H Kwok, C P Pang, et al.
Archives of Neurology|April 18, 2000
The alpha-synuclein gene and Parkinson disease in a Chinese populationD K Chan, G Mellick, H Cai, et al.
Pageof 14

Showing results (71-80 of 132) with videos related to

Sort By:
Pageof 14
Human Mutation|February 6, 1998
Possible common mutations in the low density lipoprotein receptor gene in ChineseY T Mak, J Zhang, Y S Chan, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 9, 1998
Mutations in the low-density lipoprotein receptor gene in Chinese familial hypercholesterolemia patientsY T Mak, C P Pang, B Tomlinson, et al.
Eye (London, England)|July 12, 2008
A novel mutation in CRYBB2 responsible for inherited coronary cataractD Lou, J-P Tong, L-Y Zhang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's diseaseC P Pang, J Zhang, J Woo, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
An unusual case of multiple carboxylase deficiency presenting as generalized pustular psoriasis in a Chinese boyL K Law, C Y Lau, C P Pang, et al.
The Biochemical Journal|September 15, 1984
Stereochemistry of the incorporation of valine methyl groups into methylene groups in cephalosporin CC P Pang, R L White, E P Abraham, et al.
Investigative Ophthalmology & Visual Science|May 8, 2000
Truncations in the TIGR gene in individuals with and without primary open-angle glaucomaD S Lam, Y F Leung, J K Chua, et al.
The British Journal of Ophthalmology|August 25, 2001
Rhodopsin mutations in Chinese patients with retinitis pigmentosaW M Chan, K Y Yeung, C P Pang, et al.
Eye (London, England)|March 15, 2006
An in vitro study on the compatibility and concentrations of combinations of vancomycin, amikacin, and dexamethasone in human vitreousM Hui, A K H Kwok, C P Pang, et al.
Archives of Neurology|April 18, 2000
The alpha-synuclein gene and Parkinson disease in a Chinese populationD K Chan, G Mellick, H Cai, et al.
Pageof 14