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Volume 2;  2001
Research Articles
Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice
Michael G Anderson, Richard S Smith, Olga V Savinova, Norman L Hawes, Bo Chang, Adriana Zabaleta, Robert Wilpan, John R Heckenlively, Muriel Davisson, Simon WM John
BMC Genet. 2001; 2: 1. Published online 2001 January 15. doi: 10.1186/1471-2156-2-1
PMCID:
PMC29081
Abstract Full Text PDF–1.4M
Chromosomal mapping, gene structure and characterization of the human and murine RAB27B gene
José S Ramalho, Tanya Tolmachova, Alistair N Hume, Amanda McGuigan, Cheryl Y Gregory-Evans, Clare Huxley, Miguel C Seabra
BMC Genet. 2001; 2: 2. Published online 2001 February 2. doi: 10.1186/1471-2156-2-2
PMCID:
PMC29082
Abstract Full Text PDF–1.9M
Analysis of human sarcospan as a candidate gene for CFEOM1
Kristine F O'Brien, Elizabeth C Engle, Louis M Kunkel
BMC Genet. 2001; 2: 3. Published online 2001 February 6. doi: 10.1186/1471-2156-2-3
PMCID:
PMC29083
Abstract Full Text PDF–764K
NRG1 is required for glucose repression of the SUC2 and GAL genes of Saccharomyces cerevisiae
Heng Zhou, Fred Winston
BMC Genet. 2001; 2: 5. Published online 2001 March 19. doi: 10.1186/1471-2156-2-5
PMCID:
PMC31344
Abstract Full Text PDF–1.4M
CTLA4 gene polymorphisms are associated with, and linked to, insulin-dependent diabetes mellitus in a Russian population
Dimitry A Chistiakov, Kirill V Savost'anov, Valery V Nosikov
BMC Genet. 2001; 2: 6. Published online 2001 March 27. doi: 10.1186/1471-2156-2-6
PMCID:
PMC31345
Abstract Full Text PDF–262K
The A54T polymorphism at the intestinal fatty acid binding protein 2 is associated with insulin resistance in glucose tolerant Caucasians
Ken C Chiu, Lee-Ming Chuang, Carol Yoon
BMC Genet. 2001; 2: 7. Published online 2001 March 28. doi: 10.1186/1471-2156-2-7
PMCID:
PMC31346
Abstract Full Text PDF–440K
Genomic organization and single-nucleotide polymorphism map of desmuslin, a novel intermediate filament protein on chromosome 15q26.3
Yuji Mizuno, Annibale A Puca, Kristine F O'Brien, Alan H Beggs, Louis M Kunkel
BMC Genet. 2001; 2: 8. Published online 2001 June 20. doi: 10.1186/1471-2156-2-8
PMCID:
PMC34549
Abstract Full Text PDF–450K
A missense mutation (Q279R) in the Fumarylacetoacetate Hydrolase gene, responsible for hereditary tyrosinemia, acts as a splicing mutation
Natacha Dreumont, Jacques A Poudrier, Anne Bergeron, Harvey L Levy, Faouzi Baklouti, Robert M Tanguay
BMC Genet. 2001; 2: 9. Published online 2001 June 29. doi: 10.1186/1471-2156-2-9
PMCID:
PMC35353
Abstract Full Text PDF–766K
RHD positive haplotypes in D negative Europeans
Franz F Wagner, Alexander Frohmajer, Willy A Flegel
BMC Genet. 2001; 2: 10. Published online 2001 July 16. doi: 10.1186/1471-2156-2-10
PMCID:
PMC37267
Abstract Full Text PDF–2.0M
Gene targeting in mosquito cells: a demonstration of 'knockout' technology in extrachromosomal gene arrays
Paul Eggleston, Yuguang Zhao
BMC Genet. 2001; 2: 11. Published online 2001 July 31. doi: 10.1186/1471-2156-2-11
PMCID:
PMC37536
Abstract Full Text PDF–1.1M
Intraocular pressure in genetically distinct mice: an update and strain survey
Olga V Savinova, Fumihiro Sugiyama, Janice E Martin, Stanislav I Tomarev, Beverly J Paigen, Richard S Smith, Simon WM John
BMC Genet. 2001; 2: 12. Published online 2001 August 9. doi: 10.1186/1471-2156-2-12
Correction in:
BMC Genet. 2001; 2: 16.
PMCID:
PMC48141
Abstract Full Text PDF–834K Correction
Major genomic mitochondrial lineages delineate early human expansions
Nicole Maca-Meyer, Ana M González, José M Larruga, Carlos Flores, Vicente M Cabrera
BMC Genet. 2001; 2: 13. Published online 2001 August 13. doi: 10.1186/1471-2156-2-13
PMCID:
PMC55343
Abstract Full Text PDF–582K
Somatic frameshift mutations in the Bloom syndrome BLM gene are frequent in sporadic gastric carcinomas with microsatellite mutator phenotype
George Calin, Guglielmina N Ranzani, Dino Amadori, Vlad Herlea, Irina Matei, Giuseppe Barbanti-Brodano, Massimo Negrini
BMC Genet. 2001; 2: 14. Published online 2001 August 14. doi: 10.1186/1471-2156-2-14
PMCID:
PMC48142
Abstract Full Text PDF–516K
Isozyme and allozyme markers distinguishing two morphologically similar, medically important Mastomys species (Rodentia: Muridae)
Andre A Smit, Herman FH Van der Bank
BMC Genet. 2001; 2: 15. Published online 2001 September 21. doi: 10.1186/1471-2156-2-15
PMCID:
PMC59666
Abstract Full Text PDF–816K
Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing
Richard R Bennett, Johan den Dunnen, Kristine F O'Brien, Basil T Darras, Louis M Kunkel
BMC Genet. 2001; 2: 17. Published online 2001 October 17. doi: 10.1186/1471-2156-2-17
PMCID:
PMC59832
Abstract Full Text PDF–1.4M Supplementary Material
Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure
Bo Chang, Richard S Smith, Maureen Peters, Olga V Savinova, Norman L Hawes, Adriana Zabaleta, Steven Nusinowitz, Janice E Martin, Muriel L Davisson, Constance L Cepko, Brigid LM Hogan, Simon WM John
BMC Genet. 2001; 2: 18. Published online 2001 November 6. doi: 10.1186/1471-2156-2-18
PMCID:
PMC59999
Abstract Full Text PDF–2.0M
Fusion of the NUP98 gene with the LEDGF/p52 gene defines a recurrent acute myeloid leukemia translocation
Damian J Hussey, Sarah Moore, Mario Nicola, Alexander Dobrovic
BMC Genet. 2001; 2: 20. Published online 2001 November 23. doi: 10.1186/1471-2156-2-20
PMCID:
PMC60524
Abstract Full Text PDF–334K
A sensitive and rapid assay for homologous recombination in mosquito cells: impact of vector topology and implications for gene targeting
Paul Eggleston, Yuguang Zhao
BMC Genet. 2001; 2: 21. Published online 2001 December 17. doi: 10.1186/1471-2156-2-21
PMCID:
PMC64643
Abstract Full Text PDF–719K
A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues
Thea K Chibuk, Jocelyn M Bischof, Rachel Wevrick
BMC Genet. 2001; 2: 22. Published online 2001 December 20. doi: 10.1186/1471-2156-2-22
PMCID:
PMC64493
Abstract Full Text PDF–798K
Methodology Articles
MICE, a program to track and monitor animals in animal facilities
Kim E Boulukos, Philippe Pognonec
BMC Genet. 2001; 2: 4. Published online 2001 March 8. doi: 10.1186/1471-2156-2-4
PMCID:
PMC29084
Abstract Full Text PDF–2.8M
Discrimination of three mutational events that result in a disruption of the R122 primary autolysis site of the human cationic trypsinogen (PRSS1) by denaturing high performance liquid chromatography
Cedric Le Maréchal, Jian-Min Chen, Isabelle Quéré, Odile Raguénès, Claude Férec, Jean Auroux
BMC Genet. 2001; 2: 19. Published online 2001 November 19. doi: 10.1186/1471-2156-2-19
PMCID:
PMC60523
Abstract Full Text PDF–342K
Correction
Intraocular pressure in genetically distinct mice: an update and strain survey: Correction
Olga V Savinova, Fumihiro Sugiyama, Janice E Martin, Stanislav I Tomarev, Beverly J Paigen, Richard S Smith, Simon WM John
BMC Genet. 2001; 2: 16. Published online 2001 September 26. doi: 10.1186/1471-2156-2-16
Corrects:
BMC Genet. 2001; 2: 12.
PMCID:
PMC57738
Correction PDF–156K Original Article
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