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Gynecologic Oncology
|
October 11, 2005
MRP2 (ABCC2) and cisplatin sensitivity in hepatocytes and human ovarian carcinoma
Alexander D Guminski, Rosemary L Balleine, Yoke-Eng Chiew, et al.
Plos One
|
April 3, 2008
Distinguishing molecular features and clinical characteristics of a putative new rhinovirus species, human rhinovirus C (HRV C)
Peter McErlean, Laura A Shackelton, Emily Andrews, et al.
Human Molecular Genetics
|
July 13, 2013
Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypes
Yuri V Sergeev, Susan Vitale, Paul A Sieving, et al.
International Journal of Cardiology
|
December 22, 2014
Comparison of a morning polypill, evening polypill and individual pills on LDL-cholesterol, ambulatory blood pressure and adherence in high-risk patients; a randomized crossover trial
M Lafeber, D E Grobbee, I M Schrover, et al.
Investigative Ophthalmology & Visual Science
|
July 29, 2003
Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity
Anthony G Robson, Ahmed El-Amir, Claire Bailey, et al.
Retina (Philadelphia, Pa.)
|
December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology
Anthony G Robson, Andrew R Webster, Michel Michaelides, et al.
New Zealand Veterinary Journal
|
May 31, 2007
Behavioural, biochemical, and pathological responses of possums (Trichosurus vulpecula) poisoned with phosphorus paste
C E O'Connor, K E Littin, L M Milne, et al.
Eye (London, England)
|
July 19, 2020
A clinical study of patients with novel CDHR1 genotypes associated with late-onset macular dystrophy
Rola Ba-Abbad, Anthony G Robson, Omar A Mahroo, et al.
European Journal of Human Genetics : EJHG
|
October 23, 2025
RP9 revisited; RP9 p.(H137L) remains a likely cause of dominant splicing factor-Retinitis Pigmentosa
Leon Chang, James A Poulter, Andrew R Webster, et al.
Ophthalmic Genetics
|
November 20, 2018
Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degeneration
Shyamanga Borooah, Chloe M Stanton, Joseph Marsh, et al.
Page
of 125
Search research articles
Search
Showing results (781-790 of 1,250) with videos related to
Sort By:
Page
of 125
Gynecologic Oncology
|
October 11, 2005
MRP2 (ABCC2) and cisplatin sensitivity in hepatocytes and human ovarian carcinoma
Alexander D Guminski, Rosemary L Balleine, Yoke-Eng Chiew, et al.
Plos One
|
April 3, 2008
Distinguishing molecular features and clinical characteristics of a putative new rhinovirus species, human rhinovirus C (HRV C)
Peter McErlean, Laura A Shackelton, Emily Andrews, et al.
Human Molecular Genetics
|
July 13, 2013
Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypes
Yuri V Sergeev, Susan Vitale, Paul A Sieving, et al.
International Journal of Cardiology
|
December 22, 2014
Comparison of a morning polypill, evening polypill and individual pills on LDL-cholesterol, ambulatory blood pressure and adherence in high-risk patients; a randomized crossover trial
M Lafeber, D E Grobbee, I M Schrover, et al.
Investigative Ophthalmology & Visual Science
|
July 29, 2003
Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity
Anthony G Robson, Ahmed El-Amir, Claire Bailey, et al.
Retina (Philadelphia, Pa.)
|
December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology
Anthony G Robson, Andrew R Webster, Michel Michaelides, et al.
New Zealand Veterinary Journal
|
May 31, 2007
Behavioural, biochemical, and pathological responses of possums (Trichosurus vulpecula) poisoned with phosphorus paste
C E O'Connor, K E Littin, L M Milne, et al.
Eye (London, England)
|
July 19, 2020
A clinical study of patients with novel CDHR1 genotypes associated with late-onset macular dystrophy
Rola Ba-Abbad, Anthony G Robson, Omar A Mahroo, et al.
European Journal of Human Genetics : EJHG
|
October 23, 2025
RP9 revisited; RP9 p.(H137L) remains a likely cause of dominant splicing factor-Retinitis Pigmentosa
Leon Chang, James A Poulter, Andrew R Webster, et al.
Ophthalmic Genetics
|
November 20, 2018
Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degeneration
Shyamanga Borooah, Chloe M Stanton, Joseph Marsh, et al.
Page
of 125