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Results 1 to 24 of 24

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LeishmaniasisROBERTS, Lynden J; HANDMAN, Emanuela; FOOTE, Simon J et al.BMJ. British medical journal (International ed.). 2000, Vol 321, Num 7264, pp 801-804, issn 0959-8146Article

P R E S S The role of host genetics in leishmaniasisSAKTHIANANDESWAREN, Anuratha; FOOTE, Simon J; HANDMAN, Emanuela et al.Trends in parasitology. 2009, Vol 25, Num 8, pp 383-391, issn 1471-4922, 9 p.Article

Second stage of a genome scan of schizophrenia : Study of five positive regions in an expanded sampleMOWRY, Bryan J; EWEN, Kelly R; SILVERMAN, Jeremy M et al.American journal of medical genetics. 2000, Vol 96, Num 6, pp 864-869, issn 0148-7299Article

Fine Mapping of Leishmania major Susceptibility Locus lmr2 and Evidence of a Role for Fli1 in Disease and Wound HealingSAKTHIANANDESWAREN, Anuratha; CURTIS, Joan M; ELSO, Colleen et al.Infection and immunity. 2010, Vol 78, Num 6, pp 2734-2744, issn 0019-9567, 11 p.Article

On the utility of data from the International HapMap Project for Australian association studiesSTANKOVICH, Jim; COX, Charles J; SPEED, Terence P et al.Human genetics. 2006, Vol 119, Num 1-2, pp 220-222, issn 0340-6717, 3 p.Article

Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigreeCHARLESWORTH, Jac C; DYER, Thomas D; STANKOVICH, Jim M et al.Investigative ophthalmology & visual science. 2005, Vol 46, Num 10, pp 3723-3729, issn 0146-0404, 7 p.Article

Genetic dissection of the human leukocyte antigen region by use of haplotypes of tasmanians with multiple sclerosisRUBIO, Justin P; BAHLO, Melanie; VARNEY, Mike et al.American journal of human genetics. 2002, Vol 70, Num 5, pp 1125-1137, issn 0002-9297Article

The Complete Genome Sequence of Actinobacillus pleuropneumoniae L20 (Serotype 5b)FOOTE, Simon J; BOSSE, Janine T; BOUEVITCH, Anne B et al.Journal of bacteriology. 2008, Vol 190, Num 4, pp 1495-1496, issn 0021-9193, 2 p.Article

Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosisRUBIO, Justin P; BAHLO, Melanie; TAIT, Brian et al.Human genetics. 2004, Vol 114, Num 6, pp 573-580, issn 0340-6717, 8 p.Article

An ethyl-nitrosourea-induced point mutation in Phex causes exon skipping, X-linked hypophosphatemia, and ricketsCARPINELLI, Marina R; WICKS, Ian P; SIMS, Natalie A et al.The American journal of pathology. 2002, Vol 161, Num 5, pp 1925-1933, issn 0002-9440, 9 p.Article

Anticipation in familial hematologic malignanciesTEGG, Elizabeth M; THOMSON, Russell J; STANKOVICH, Jim M et al.Blood. 2011, Vol 117, Num 4, pp 1308-1310, issn 0006-4971, 3 p.Article

Proteomic insights into cold adaptation of psychrotrophic and mesophilic Acidithiobacillus ferrooxidans strainsMYKYTCZUK, Nadia C. S; TREVORS, Jack T; FOOTE, Simon J et al.Antonie van Leeuwenhoek. 2011, Vol 100, Num 2, pp 259-277, issn 0003-6072, 19 p.Article

Novel roles for erythroid Ankyrin-1 revealed through an ENU-induced null mouse mutantRANK, Gerhard; SUTTON, Rosemary; CRABB, Brendan S et al.Blood. 2009, Vol 113, Num 14, pp 3352-3362, issn 0006-4971, 11 p.Article

Detecting genome wide haplotype sharing using SNP or microsatellite haplotype dataBAHLO, Melanie; STANKOVICH, Jim; SPEED, Terence P et al.Human genetics. 2006, Vol 119, Num 1-2, pp 38-50, issn 0340-6717, 13 p.Article

Mapping of the Plasmodium chabaudi resistance locus char2LIN, Enmoore; PAPPENFUSS, Tony; TAN, Rachel B et al.Infection and immunity. 2006, Vol 74, Num 10, pp 5814-5819, issn 0019-9567, 6 p.Article

PU. 1 is a suppressor of myeloid leukemia, inactivated in mice by gene deletion and mutation of its DNA binding domainCOOK, Wendy D; MCCAW, Benjamin J; HERRING, Christopher et al.Blood. 2004, Vol 104, Num 12, pp 3437-3444, issn 0006-4971, 8 p.Article

Platelet Factor 4 and Duffy Antigen Required for Platelet Killing of Plasmodium falciparumMCMORRAN, Brendan J; WIECZORSKI, Laura; DRYSDALE, Karen E et al.Science (Washington, D.C.). 2012, Vol 338, Num 6112, pp 1348-1351, issn 0036-8075, 4 p.Article

Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypesTEGG, Elizabeth M; THOMSON, Russell J; LOWENTHAL, Ray M et al.British journal of haematology. 2010, Vol 150, Num 4, pp 456-462, issn 0007-1048, 7 p.Article

Platelets Kill Intraerythrocytic Malarial Parasites and Mediate Survival to InfectionMCMORRAN, Brendan J; MARSHALL, Vikki M; DE GRAAF, Carolyn et al.Science (Washington, D.C.). 2009, Vol 323, Num 5915, pp 797-800, issn 0036-8075, 4 p.Article

Decreases in HCN mRNA expression in the hippocampus after kindling and status epilepticus in adult ratsPOWELL, Kim L; NG, Caroline; O'BRIEN, Terence J et al.Epilepsia (Copenhagen). 2008, Vol 49, Num 10, pp 1686-1695, issn 0013-9580, 10 p.Article

Evidence for a novel glaucoma locus at chromosome 3p21-22BAIRD, Paul N; FOOTE, Simon J; MACKEY, David A et al.Human genetics. 2005, Vol 117, Num 2-3, pp 249-257, issn 0340-6717, 9 p.Article

Identifying nineteenth century genealogical links from genotypesSTANKOVICH, Jim; BAHIO, Melanie; RUBIO, Justin P et al.Human genetics. 2005, Vol 117, Num 2-3, pp 188-199, issn 0340-6717, 12 p.Article

Analysis of 15 primary open-angle glaucoma families from Australia identifies a founder effect for the Q368ST0P mutation of myocilinBAIRD, Paul N; CRAIG, Jamie E; RICHARDSON, Andrea J et al.Human genetics. 2003, Vol 112, Num 2, pp 110-116, issn 0340-6717, 7 p.Article

Mice that are congenic for the char2 locus are susceptible to malariaBURT, Rachel A; MARSHALL, Vikki M; WAGGLEN, Jamie et al.Infection and immunity. 2002, Vol 70, Num 8, pp 4750-4753, issn 0019-9567, 4 p.Article

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