H. Gornall

发表

Synonymous Mutations in RNASEH2A Create Cryptic Splice Sites Impairing RNase H2 Enzyme Function in Aicardi–Goutières Syndrome

Martin A. M. Reijns, L. Lagae, B. Gener, 2013, Human mutation.

Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

L. Lagae, A. Vanderver, K. Devriendt, 2015, American journal of medical genetics. Part A.

CAR T cells: driving the road from the laboratory to the clinic

D. Gilham, R. Hawkins, H. Gornall, 2014, Immunological reviews.

CCR7+ selected gene-modified T cells maintain a central memory phenotype and display enhanced persistence in peripheral blood in vivo

D. Gilham, R. Hawkins, H. Gornall, 2017, Journal of Immunotherapy for Cancer.

Potential limitations of the NSG humanized mouse as a model system to optimize engineered human T cell therapy for cancer.

D. Gilham, R. Hawkins, H. Gornall, 2013, Human gene therapy methods.

Intracerebral large artery disease in Aicardi–Goutières syndrome implicates SAMHD1 in vascular homeostasis

Y. Crow, D. Mitra, B. Bernardi, 2010, Developmental medicine and child neurology.

Tartrate resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature

F. Rieux-Laucat, J. Casanova, S. Lovell, 2010, Nature Genetics.

Familial Aicardi–Goutières syndrome due to SAMHD1 mutations is associated with chronic arthropathy and contractures

Y. Crow, G. Rice, D. Singh-Grewal, 2010, American journal of medical genetics. Part A.

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

Jonathan C. Fuller, D. Bonthron, E. Bertini, 2009, Nature Genetics.

Chilblains as a diagnostic sign of aicardi-goutières syndrome.

Y. Crow, P. Lebon, G. Rice, 2010, Neuropediatrics.

Definition and application of good manufacturing process-compliant production of CEA-specific chimeric antigen receptor expressing T-cells for phase I/II clinical trial

R. Guest, F. Thistlethwaite, D. Gilham, 2014, Cancer Immunology, Immunotherapy.

P270 Moyamoya syndrome and peripheral vascular disease due to mutation in newly described Aicardi Goutieres syndrome 5 gene SAMHD1

Y. Crow, D. Mitra, V. Ramesh, 2009 .

CAR T cells: driving the road from the laboratory to the clinic

D. Gilham, R. Hawkins, H. Gornall, 2014, Immunological reviews.

Intracerebral large artery disease in Aicardi–Goutières syndrome implicates SAMHD1 in vascular homeostasis

Y. Crow, D. Mitra, B. Bernardi, 2010, Developmental medicine and child neurology.