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Mackay, Donna
112  Ergebnisse:
Personensuche X
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1

Characterisation and Validation of Insertions and Deletions..:

Lescai, Francesco ; Bonfiglio, Silvia ; Bacchelli, Chiara...
PLoS ONE.  7 (2012)  12 - p. e51292 , 2012
Link: https://doi.org/10.1371/..
 
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2

Focus on molecules: Retinol dehydrogenase 12 (RDH12):

Moradi, Phillip ; Mackay, Donna ; Hunt, David M..
Experimental Eye Research.  87 (2008)  3 - p. 160-161 , 2008
Link: https://doi.org/10.1016/..
 
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3

Disruption of lens fiber cell architecture in mice expressi..:

Shiels, Alan ; Mackay, Donna ; Bassnett, Steven..
The FASEB Journal.  14 (2000)  14 - p. 2207-2212 , 2000
Link: https://doi.org/10.1096/..
 
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4

Connexin 50 mutation in a family with congenital "zonular n..:

Berry, Vanita ; Mackay, Donna ; Khaliq, Shagufta...
Human Genetics.  105 (1999)  1-2 - p. 168-170 , 1999
Link: https://doi.org/10.1007/..
 
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5

Binding to isolated phage receptors and λ DNA release in vi..:

Mackay, Donna J. ; Bode, Vernon C.
Virology.  72 (1976)  1 - p. 167-181 , 1976
Link: https://doi.org/10.1016/..
 
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6

Events in lambda injection between phage adsorption and DNA..:

Mackay, Donna J. ; Bode, Vernon C.
Virology.  72 (1976)  1 - p. 154-166 , 1976
Link: https://doi.org/10.1016/..
 
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7

Distinction between far- and near-ultraviolet light killing..:

Ferron, W.L. ; Eisenstark, A. ; Mackay, Donna
Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis.  277 (1972)  3 - p. 651-658 , 1972
Link: https://doi.org/10.1016/..
 
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8

Exome Sequencing Identifies a Missense Variant in EFEMP1 Co..:

Mackay, Donna S. ; Bennett, Thomas M. ; Shiels, Alan.
PLOS ONE.  10 (2015)  7 - p. e0132529 , 2015
Link: https://doi.org/10.1371/..
 
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9

Exome sequencing identifies novel and recurrent mutations i..:

Mackay, Donna S ; Bennett, Thomas M ; Culican, Susan M.
Human Genomics.  8 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
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10

Mutation of the Melastatin-Related Cation Channel, TRPM3, U..:

Bennett, Thomas M. ; Mackay, Donna S. ; Siegfried, Carla J...
PLoS ONE.  9 (2014)  8 - p. e104000 , 2014
Link: https://doi.org/10.1371/..
 
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11

A Homozygous Mutation in theTUBGene Associated with Retinal..:

Borman, Arundhati Dev ; Pearce, Laura R. ; Mackay, Donna S....
Human Mutation.  35 (2013)  3 - p. 289-293 , 2013
Link: https://doi.org/10.1002/..
 
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12

Screening of a Large Cohort of Leber Congenital Amaurosis a..:

Mackay, Donna S. ; Borman, Arundhati Dev ; Sui, Ruifang...
Human Mutation.  35 (2013)  1 - p. 150-150 , 2013
Link: https://doi.org/10.1002/..
 
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13

A Longitudinal Study of Stargardt Disease: Clinical and Ele..:

Fujinami, Kaoru ; Lois, Noemi ; Davidson, Alice E....
American Journal of Ophthalmology.  155 (2013)  6 - p. 1075-1088.e13 , 2013
Link: https://doi.org/10.1016/..
 
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14

A novel α-synuclein missense mutation in Parkinson disease:

Proukakis, Christos ; Dudzik, Christopher G. ; Brier, Timothy...
Neurology.  80 (2013)  11 - p. 1062-1064 , 2013
Link: https://doi.org/10.1212/..
 
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15

Screening of a Large Cohort of Leber Congenital Amaurosis a..:

Mackay, Donna S. ; Borman, Arundhati Dev ; Sui, Ruifang...
Human Mutation.  34 (2013)  11 - p. 1537-1546 , 2013
Link: https://doi.org/10.1002/..
 
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