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Judith A Goodship

Showing results (11-20 of 57) with videos related to

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Molecular Immunology|August 3, 2005
Does complement factor B have a role in the pathogenesis of atypical HUS?David Kavanagh, Elizabeth J Kemp, Anna Richards, et al.
Pediatric Nephrology (Berlin, Germany)|July 2, 2003
Successful (?) therapy of hemolytic-uremic syndrome with factor H abnormalityAngela Gerber, Antje H Kirchhoff-Moradpour, Silke Obieglo, et al.
BMC Biology|March 2, 2011
Evc2 is a positive modulator of Hedgehog signalling that interacts with Evc at the cilia membrane and is also found in the nucleusHelen J Blair, Stuart Tompson, Yu-Ning Liu, et al.
BMC Medical Genetics|June 5, 2015
Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case reportEmma Montgomery, John A Sayer, Laura A Baines, et al.
Plos One|April 25, 2013
Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32Lucy V Holmes, Lisa Strain, Scott J Staniforth, et al.
Human Genetics|October 7, 2006
Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis-van Creveld syndrome patientsStuart W J Tompson, Victor L Ruiz-Perez, Helen J Blair, et al.
Plos One|December 11, 2013
A nonsense mutation in the IKBKG gene in mares with incontinentia pigmentiRachel E Towers, Leonardo Murgiano, David S Millar, et al.
The Journal of Experimental Medicine|January 5, 2006
Disparate roles of ATR and ATM in immunoglobulin class switch recombination and somatic hypermutationQiang Pan-Hammarström, Aleksi Lähdesmäki, Yaofeng Zhao, et al.
Journal of the American Society of Nephrology : JASN|May 27, 2005
Mutations in complement factor I predispose to development of atypical hemolytic uremic syndromeDavid Kavanagh, Elizabeth J Kemp, Elizabeth Mayland, et al.
Development (Cambridge, England)|July 31, 2007
Evc is a positive mediator of Ihh-regulated bone growth that localises at the base of chondrocyte ciliaVictor L Ruiz-Perez, Helen J Blair, M Elena Rodriguez-Andres, et al.
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
Molecular Immunology|August 3, 2005
Does complement factor B have a role in the pathogenesis of atypical HUS?David Kavanagh, Elizabeth J Kemp, Anna Richards, et al.
Pediatric Nephrology (Berlin, Germany)|July 2, 2003
Successful (?) therapy of hemolytic-uremic syndrome with factor H abnormalityAngela Gerber, Antje H Kirchhoff-Moradpour, Silke Obieglo, et al.
BMC Biology|March 2, 2011
Evc2 is a positive modulator of Hedgehog signalling that interacts with Evc at the cilia membrane and is also found in the nucleusHelen J Blair, Stuart Tompson, Yu-Ning Liu, et al.
BMC Medical Genetics|June 5, 2015
Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case reportEmma Montgomery, John A Sayer, Laura A Baines, et al.
Plos One|April 25, 2013
Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32Lucy V Holmes, Lisa Strain, Scott J Staniforth, et al.
Human Genetics|October 7, 2006
Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis-van Creveld syndrome patientsStuart W J Tompson, Victor L Ruiz-Perez, Helen J Blair, et al.
Plos One|December 11, 2013
A nonsense mutation in the IKBKG gene in mares with incontinentia pigmentiRachel E Towers, Leonardo Murgiano, David S Millar, et al.
The Journal of Experimental Medicine|January 5, 2006
Disparate roles of ATR and ATM in immunoglobulin class switch recombination and somatic hypermutationQiang Pan-Hammarström, Aleksi Lähdesmäki, Yaofeng Zhao, et al.
Journal of the American Society of Nephrology : JASN|May 27, 2005
Mutations in complement factor I predispose to development of atypical hemolytic uremic syndromeDavid Kavanagh, Elizabeth J Kemp, Elizabeth Mayland, et al.
Development (Cambridge, England)|July 31, 2007
Evc is a positive mediator of Ihh-regulated bone growth that localises at the base of chondrocyte ciliaVictor L Ruiz-Perez, Helen J Blair, M Elena Rodriguez-Andres, et al.
Pageof 6