Publications by authors named "Heema Patel"

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Strategy for the creation of clinical grade hESC line banks that HLA-match a target population.
Laureen Jacquet, Emma Stephenson, Robert Collins, Heema Patel, Jane Trussler

EMBO Mol Med· January 2013

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Derivation and feeder-free propagation of human embryonic stem cells under xeno-free conditions.
Dusko Ilic, Emma Stephenson, Victoria Wood, Laureen Jacquet, Danielle Stevenson, Heema Patel

Cytotherapy· January 2012

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Safety paradigm: genetic evaluation of therapeutic grade human embryonic stem cells.
Emma Stephenson, Caroline Mackie Ogilvie, Heema Patel, Glenda Cornwell, Laureen Jacquet

J R Soc Interface· December 2010

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Defective mitochondrial mRNA maturation is associated with spastic ataxia.
Andrew H Crosby, Heema Patel, Barry A Chioza, Christos Proukakis, Kay Gurtz

Am J Hum Genet· November 2010

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Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration.
Maria K Tsaousidou, Karim Ouahchi, Tom T Warner, Yi Yang, Michael A Simpson, Heema Patel

Am J Hum Genet· February 2008

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Endogenous spartin, mutated in hereditary spastic paraplegia, has a complex subcellular localization suggesting diverse roles in neurons.
Dimitri Robay, Heema Patel, Michael A Simpson, Nigel A Brown, Andrew H Crosby

Exp Cell Res· September 2006

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A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia.
Johanna A Reed, Phillip A Wilkinson, Heema Patel, Michael A Simpson, Arnaud Chatonnet

Neurogenetics· May 2005

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A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia.
Thomas T Warner, Heema Patel, Christos Proukakis, Johanna A Reed, Laura McKie

J Neurol· September 2004

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Troyer syndrome revisited. A clinical and radiological study of a complicated hereditary spastic paraplegia.
Christos Proukakis, Harold Cross, Heema Patel, Michael A Patton, Alan Valentine

J Neurol· September 2004

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Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome.
Christian Windpassinger, Michaela Auer-Grumbach, Joy Irobi, Heema Patel, Erwin Petek

Nat Genet· March 2004

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The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia.
Francesca D Ciccarelli, Christos Proukakis, Heema Patel, Harold Cross, Shakil Azam

Genomics· April 2003

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SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.
Heema Patel, Harold Cross, Christos Proukakis, Ruth Hershberger, Peer Bork

Nat Genet· August 2002

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