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Tom Hearn

Research Profile

Disorders

Alstrom's Syndrome

Anatomy

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Physiology

Genes & Molecular Sequences

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Fluorescence In Situ Hybridization

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Publications

TOP 3
Cosma Spalluto; David I Wilson; Tom Hearn
Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition.
Victoria J Knorz; Cosma Spalluto; Mark Lessard; Tracey L Purvis; Fiona F Adigun; Gayle B Collin; Neil A Hanley; David I Wilson; Tom Hearn
Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731.
Tracey L Purvis; Tom Hearn; Cosma Spalluto; Victoria J Knorz; Karen Piper Hanley; Tilman Sanchez-Elsner; Neil A Hanley; David I Wilson
Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1.

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All Publications

2012: Cosma Spalluto; David I Wilson; Tom Hearn
Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition.
European journal of cell biology 2012;91(9):675-86.
2010: Victoria J Knorz; Cosma Spalluto; Mark Lessard; Tracey L Purvis; Fiona F Adigun; Gayle B Collin; Neil A Hanley; David I Wilson; Tom Hearn
Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731.
Molecular biology of the cell 2010;21(21):3617-29.
2010: Tracey L Purvis; Tom Hearn; Cosma Spalluto; Victoria J Knorz; Karen Piper Hanley; Tilman Sanchez-Elsner; Neil A Hanley; David I Wilson
Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1.
Gene 2010;460(1-2):20-9.
2007: Jan D Marshall; Elizabeth G Hinman; Gayle B Collin; Sebastian Beck; Rita Cerqueira; Pietro Maffei; Gabriella Milan; Weidong Zhang; David I Wilson; Tom Hearn; Purificação Tavares; Roberto Vettor; Caterina Veronese; Mitchell Martin; W Venus So; Patsy M Nishina; Jürgen K Naggert
Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alström syndrome.
Human mutation 2007;28(11):1114-23.
2005: Tom Hearn; Cosma Spalluto; Victoria J Phillips; Glenn L Renforth; Nane Copin; Neil A Hanley; David I Wilson
Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes.
Diabetes 2005;54(5):1581-7.
2003: Sarah Brickwood; David T Bonthron; L I Al-Gazali; Karen Piper; Tom Hearn; David I Wilson; Neil A Hanley
Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3.
Journal of medical genetics 2003;40(9):685-9.
2003: Jane Guy; Tom Hearn; Moira Crosier; Jonathan M Mudge; Luigi Viggiano; Dirk Koczan; Hans-Jurgen Thiesen; Jeffrey A Bailey; Julie E Horvath; Evan E Eichler; Mark E Earthrowl; Panos Deloukas; Lisa French; Jane Rogers; David Bentley; Michael S Jackson
Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p.
Genome research 2003;13(2):159-72.
2002: Tom Hearn; Glenn L Renforth; Cosma Spalluto; Neil A Hanley; Karen Piper; Sarah Brickwood; Chris White; Vincent Connolly; James F N Taylor; Isabelle Russell-Eggitt; Dominque Bonneau; Mark Walker; David I Wilson
Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome.
Nature genetics 2002;31(1):79-83.
2002: Helen M Phillips; Glenn L Renforth; Cosma Spalluto; Tom Hearn; Andrew R J Curtis; Lyndsey Craven; Beatrice Havarani; Mark Clement-Jones; Carol English; Oliver Stumper; Tony Salmon; Susie Hutchinson; Michael S Jackson; David I Wilson
Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis.
Genomics 2002;79(4):475-8.
2002: Moira Crosier; Luigi Viggiano; Jane Guy; Doriana Misceo; Robert Stones; Wenbin Wei; Tom Hearn; ventura Mario; Nicoletta Archidiacono; Mariano Rocchi; Michael S Jackson
Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms.
Genome research 2002;12(1):67-80.
2000: Jane Guy; Cosma Spalluto; A McMurray; Tom Hearn; Moira Crosier; Luigi Viggiano; V Miolla; Nicoletta Archidiacono; Mariano Rocchi; C Scott; P A Lee; John E Sulston; J Rogers; David Bentley; Michael S Jackson
Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10q.
Human molecular genetics 2000;9(13):2029-42.
1999: Michael S Jackson; Mariano Rocchi; G Thompson; Tom Hearn; Moira Crosier; Jane Guy; D Kirk; L Mulligan; AS Ricco; S Piccininni; R Marzella; Luigi Viggiano; Nicoletta Archidiacono
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.
Human molecular genetics 1999;8(2):205-15.