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Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

Molecular psychiatry, 2012-11, Vol.17 (11), p.1103-1115

2012

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Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

Leukemia, 2010-01, Vol.24 (1), p.242-246

2010

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A tale of two siblings: two cases of AML arising from a single pre-leukemic DNMT3A mutant clone

Leukemia, 2015-10, Vol.29 (10), p.2101-2104

2015

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A novel, somatic, transforming mutation in the extracellular domain of Epidermal Growth Factor Receptor identified in myeloproliferative neoplasm

Scientific reports, 2017-05, Vol.7 (1), p.2467-9, Article 2467

2017

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Urocortin 3 transgenic mice exhibit a metabolically favourable phenotype resisting obesity and hyperglycaemia on a high-fat diet

Diabetologia, 2011-09, Vol.54 (9), p.2392-2403

2011

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Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes

Leukemia, 2018-01, Vol.32 (1), p.194-202

2018

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Bodyweight change aids prediction of survival in chronic equine grass sickness

Equine veterinary journal, 2016-11, Vol.48 (6), p.792-797

2016

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Characterisation of a compound in-cis GATA2 germline mutation in a pedigree presenting with myelodysplastic syndrome/acute myeloid leukemia with concurrent thrombocytopenia

Leukemia, 2015-08, Vol.29 (8), p.1795-1797

2015

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Delayed diagnosis leading to accelerated-phase chronic eosinophilic leukemia due to a cytogenetically cryptic, imatinib-responsive TNIP1-PDFGRB fusion gene

Leukemia, 2016-06, Vol.30 (6), p.1402-1405

2016

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ARMC5 is not implicated in familial hyperaldosteronism type II (FH-II)

Journal of human hypertension, 2017-12, Vol.31 (12), p.857-859

2017

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Central neuropathology of equine grass sickness

Acta neuropathologica, 2001-08, Vol.102 (2), p.153-159

2001

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Expression profiling reveals functionally important genes and coordinately regulated signaling pathway genes during in vitro angiogenesis

Physiological genomics, 2005-06, Vol.22 (1), p.57-69

2005

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Neuropathological lesions resembling equine grass sickness in rabbits

Veterinary record, 2005-06, Vol.156 (24), p.778-779

2005

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Phenylephrine eyedrops as a diagnostic test in equine grass sickness

Veterinary record, 2000-11, Vol.147 (21), p.603-606

2000

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Horses on pasture may be affected by equine motor neuron disease

Equine veterinary journal, 2006, Vol.38 (1), p.47-51

2006

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Polyneuritis equi: the role of T-lymphocytes and importance of differential clinical signs

Equine veterinary journal, 2008-03, Vol.40 (2), p.100-100

Hahn, C.N

2008

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glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breeds

Equine veterinary journal, 2009-07, Vol.41 (6), p.597-601

2009

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Thoracolaryngeal reflex latencies in Thoroughbred horses with recurrent laryngeal neuropathy

The veterinary journal (1997), 2005-07, Vol.170 (1), p.67-76

2005

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Histological and histochemical characterisation of the equine soft palate muscles

Equine veterinary journal, 2010-07, Vol.42 (5), p.431-437

2010

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Histological and ultrastructural evidence that recurrent laryngeal neuropathy is a bilateral mononeuropathy limited to recurrent laryngeal nerves

Equine veterinary journal, 2008-11, Vol.40 (7), p.666-672

2008

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Observations on the Interstitial Cells of Cajal and Neurons in a Recovered Case of Equine Dysautonomia (Grass Sickness)

Journal of comparative pathology, 2005-07, Vol.133 (1), p.33-40

2005

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The manic horse

Equine veterinary education, 2013-04, Vol.25 (4), p.171-172

2013

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Lack of PPCA Expression only Partially Coincides with Lysosomal Storage in Galactosialidosis Mice: Indirect Evidence for Spatial Requirement of the Catalytic Rather than the Protective Function of PPCA

Human molecular genetics, 1998-10, Vol.7 (11), p.1787-1794

1998

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Osteoblast gene expression in rat long bones: effects of ovariectomy and dihydrotestosterone on mRNA levels

Calcified tissue international, 2000-07, Vol.67 (1), p.75-79

2000

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Recurrent laryngeal neuropathy (RLN) research: Where are we and to where are we heading?

Equine veterinary journal, 2009-04, Vol.41 (4), p.324-327

2009

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Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

A tale of two siblings: two cases of AML arising from a single pre-leukemic DNMT3A mutant clone

A novel, somatic, transforming mutation in the extracellular domain of Epidermal Growth Factor Receptor identified in myeloproliferative neoplasm

Urocortin 3 transgenic mice exhibit a metabolically favourable phenotype resisting obesity and hyperglycaemia on a high-fat diet

Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes

Bodyweight change aids prediction of survival in chronic equine grass sickness

Characterisation of a compound in-cis GATA2 germline mutation in a pedigree presenting with myelodysplastic syndrome/acute myeloid leukemia with concurrent thrombocytopenia

Delayed diagnosis leading to accelerated-phase chronic eosinophilic leukemia due to a cytogenetically cryptic, imatinib-responsive TNIP1-PDFGRB fusion gene

ARMC5 is not implicated in familial hyperaldosteronism type II (FH-II)

Central neuropathology of equine grass sickness

Expression profiling reveals functionally important genes and coordinately regulated signaling pathway genes during in vitro angiogenesis

Neuropathological lesions resembling equine grass sickness in rabbits

Phenylephrine eyedrops as a diagnostic test in equine grass sickness

Horses on pasture may be affected by equine motor neuron disease

Polyneuritis equi: the role of T-lymphocytes and importance of differential clinical signs

glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breeds

Thoracolaryngeal reflex latencies in Thoroughbred horses with recurrent laryngeal neuropathy

Histological and histochemical characterisation of the equine soft palate muscles

Histological and ultrastructural evidence that recurrent laryngeal neuropathy is a bilateral mononeuropathy limited to recurrent laryngeal nerves

Observations on the Interstitial Cells of Cajal and Neurons in a Recovered Case of Equine Dysautonomia (Grass Sickness)

The manic horse

Lack of PPCA Expression only Partially Coincides with Lysosomal Storage in Galactosialidosis Mice: Indirect Evidence for Spatial Requirement of the Catalytic Rather than the Protective Function of PPCA

Osteoblast gene expression in rat long bones: effects of ovariectomy and dihydrotestosterone on mRNA levels

Recurrent laryngeal neuropathy (RLN) research: Where are we and to where are we heading?

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