T. Hearn

发表

Sequences flanking the centromere of human chromosome 10 are a complex patchwork of arm-specific sequences, stable duplications and unstable sequences with homologies to telomeric and other centromeric locations.

N. Archidiacono, M. Rocchi, M. Jackson, 1999, Human molecular genetics.

Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3

T. Hearn, S. Brickwood, K. Piper, 2003, Journal of medical genetics.

Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition.

David I. Wilson, T. Hearn, C. Spalluto, 2012, European journal of cell biology.

Evidence for reciliation of RPE1 cells in late G1 phase, and ciliary localisation of cyclin B1

David I. Wilson, T. Hearn, C. Spalluto, 2013, FEBS open bio.

Evidence for centriolar satellite localization of CDK1 and cyclin B2

David I. Wilson, T. Hearn, C. Spalluto, 2013, Cell cycle.

Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10q.

J. Sulston, D. Bentley, J. Rogers, 2000, Human molecular genetics.

Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p.

Jonathan M. Mudge, Dirk Koczan, Panos Deloukas, 2003, Genome research.

Elevated oxysterol levels in human and mouse livers reflect nonalcoholic steatohepatitis[S]

T. Hearn, G. Rogler, E. Maggio, 2019, Journal of Lipid Research.

Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1

David I. Wilson, T. Hearn, C. Spalluto, 2010, Gene.

ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits

T. Hearn, 2018, Journal of Molecular Medicine.

Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis.

David I. Wilson, M. Jackson, T. Hearn, 2002, Genomics.

Centriolar Association of ALMS1 and Likely Centrosomal Functions of the ALMS Motif–containing Proteins C10orf90 and KIAA1731

David I. Wilson, T. Hearn, C. Spalluto, 2010, Molecular biology of the cell.

Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes.

David I. Wilson, T. Hearn, C. Spalluto, 2005, Diabetes.

Subcellular Localization of ALMS 1 Supports Involvement of Centrosome and Basal Body Dysfunction in the Pathogenesis of Obesity , Insulin Resistance , and Type 2 Diabetes

David I. Wilson, T. Hearn, C. Spalluto, 2005 .

Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome

David I. Wilson, M. Walker, T. Hearn, 2002, Nature Genetics.

In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets

David I. Wilson, S. Ellard, T. Hearn, 2010, The Journal of endocrinology.

Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms.

N. Archidiacono, D. Misceo, M. Rocchi, 2002, Genome research.

Development of the Human Pancreas From Foregut to Endocrine Commitment

T. Hearn, N. Hanley, N. Roberts, 2013, Diabetes.

Spectrum of ALMS1 variants and evaluation of genotype‐phenotype correlations in Alström syndrome

W. V. So, J. Naggert, T. Hearn, 2007, Human mutation.

Elevated oxysterol levels in human and mouse livers reflect nonalcoholic steatohepatitis

T. Hearn, G. Rogler, E. Maggio, 2019, Journal of Lipid Research.