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Search Results - Clover, Gillian M.
Search Results - Clover, Gillian M.
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A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation
by
Hemara-Wahanui, Ariana
,
Berjukow, Stanislav
,
Hope, Carolyn I
,
Dearden, Peter K
,
Wu, Shu-Biao
,
Wilson-Wheeler, Jane
,
Sharp, Dianne M
,
Lundon-Treweek, Patricia
,
Clover, Gillian M
,
Hoda, Jean-Charles
,
Striessnig, Jörg
,
Marksteiner, Rainer
,
Hering, Steffen
,
Maw, Marion A
Published in
Proceedings of the National Academy of Sciences - PNAS
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Confocal imaging of the human keratocyte network using the vital dye 5-chloromethylfluorescein diacetate
by
Poole, C Anthony
,
Brookes, Nigel H
,
Clover, Gillian M
Published in
Clinical & experimental ophthalmology
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Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2
by
Hope, Carolyn I
,
Sharp, Dianne M
,
Hemara-Wahanui, Ariana
,
Sissingh, Jennifer I
,
Lundon, Patricia
,
Mitchell, Ed A
,
Maw, Marion A
,
Clover, Gillian M
Published in
Clinical & experimental ophthalmology
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A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Ca v 1.4 channel activation
by
Hemara-Wahanui, Ariana
,
Berjukow, Stanislav
,
Hope, Carolyn I.
,
Dearden, Peter K.
,
Wu, Shu-Biao
,
Wilson-Wheeler, Jane
,
Sharp, Dianne M.
,
Lundon-Treweek, Patricia
,
Clover, Gillian M.
,
Hoda, Jean-Charles
,
Striessnig, Jörg
,
Marksteiner, Rainer
,
Hering, Steffen
,
Maw, Marion A.
Published in
Proceedings of the National Academy of Sciences - PNAS
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A CACNA1F Mutation Identified in an X-Linked Retinal Disorder Shifts the Voltage Dependence of Ca v1.4 Channel Activation
by
Hemara-Wahanui, Ariana
,
Berjukow, Stanislav
,
Hope, Carolyn I.
,
Dearden, Peter K.
,
Wu, Shu-Biao
,
Wilson-Wheeler, Jane
,
Sharp, Dianne M.
,
Lundon-Treweek, Patricia
,
Clover, Gillian M.
,
Hoda, Jean-Charles
,
Striessnig, Jörg
,
Marksteiner, Rainer
,
Hering, Steffen
,
Maw, Marion A.
,
Campbell, Kevin P.
Published in
Proceedings of the National Academy of Sciences - PNAS
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A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Ca sub(v)1.4 channel activation
by
Hemara-Wahanui, Ariana
,
Berjukow, Stanislav
,
Hope, Carolyn I
,
Dearden, Peter K
,
Wu, Shu-Biao
,
Wilson-Wheeler, Jane
,
Sharp, Dianne M
,
Lundon-Treweek, Patricia
,
Clover, Gillian M
,
Hoda, Jean-Charles
,
Striessnig, Joerg
,
Marksteiner, Rainer
,
Hering, Steffen
,
Maw, Marion A
Published in
Proceedings of the National Academy of Sciences - PNAS
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Article
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Proceedings Of The National Academy Of Sciences - Pnas
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Clinical & Experimental Ophthalmology
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Calcium Channels, L-Type - Genetics
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5-Chloromethylfluorescein Diacetate
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