BMC Genetics - oalib

OALib Journal期刊
ISSN: 2333-9721
费用：99美元

投递稿件

为什么选择我们？ >>

- 开源期刊

- 同行审议

- 快速出刊

- 终身存储

- 免费检索

- 免费推广

- 更多...

- 搜索引擎

BMC Genetics

ISSN Print: 1471-2156

ISSN Online:

主页: http://www.biomedcentral.com/bmcgenet

分享:

Characterization of rabbit myocilin: Implications for human myocilin glycosylation and signal peptide usage

Allan R Shepard, Nasreen Jacobson, Ruifang Sui, H Thomas Steely, Andrew J Lotery, Edwin M Stone, Abbot F Clark

Gene structure and chromosomal localization of mouse Opa1 : its exclusion from the Bst locus

Cécile Delettre, Guy Lenaers, Pascale Belenguer, Christian P Hamel

Mitochondrial DNA transit between West Asia and North Africa inferred from U6 phylogeography

Nicole Maca-Meyer, Ana M González, José Pestano, Carlos Flores, José M Larruga, Vicente M Cabrera

RHD allele distribution in Africans of Mali

Franz F Wagner, Joann M Moulds, Anatole Tounkara, Bourema Kouriba, Willy A Flegel

Parasexual genetics of Dictyostelium gene disruptions: identification of a ras pathway using diploids

Jason King, Robert H Insall

Study of human SP-A, SP-B and SP-D loci: allele frequencies, linkage disequilibrium and heterozygosity in different races and ethnic groups

Wenlei Liu, Christy M Bentley, Joanna Floros

Male preponderance in early diagnosed type 2 diabetes is associated with the ARE insertion/deletion polymorphism in the PPP1R3A locus

Alex SF Doney, Bettina Fischer, Joanne E Cecil, Patricia TW Cohen, Douglas I Boyle, Graham Leese, Andrew D Morris, Colin NA Palmer

Involvement of an SCFSlmb complex in timely elimination of E2F upon initiation of DNA replication in Drosophila

Jean-Karim Hériché, Dan Ang, Ethan Bier, Patrick H O'Farrell

Identification of three novel OA1 gene mutations identified in three families misdiagnosed with congenital nystagmus and carrier status determination by real-time quantitative PCR assay

Valérie Faugère, Sylvie Tuffery-Giraud, Christian Hamel, Mireille Claustres

Intersection tests for single marker QTL analysis can be more powerful than two marker QTL analysis

Cynthia J Coffman, RW Doerge, Marta L Wayne, Lauren M McIntyre

Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study

Byng Martyn C,Fisher Sheila A,Lewis Cathryn M,Whittaker John C

Genetic Analysis Workshop 13: Analysis of Longitudinal Family Data for Complex Diseases and Related Risk Factors

Almasy Laura,Amos Christopher I,Bailey-Wilson Joan E,Cantor Rita M

Multiple telophase arrest bypassed (tab) mutants alleviate the essential requirement for Cdc15 in exit from mitosis in S. cerevisiae

Wenying Shou, Raymond J Deshaies

CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX

Elizabeth C Engle, Nathalie McIntosh, Koki Yamada, Bjorn A Lee, Roger Johnson, Michael O'Keefe, Robert Letson, Arnold London, Evan Ballard, Mark Ruttum, Naomichi Matsumoto, Nakamichi Saito, Mary Collins, Lisa Morris, Monte Monte, Adriano Magli, Teresa de Berardinis

The human homologue of unc-93 maps to chromosome 6q27 – characterisation and analysis in sporadic epithelial ovarian cancer

Ying Liu, Phillippa Dodds, Gracy Emilion, Andrew J Mungall, Ian Dunham, Stephan Beck, R Spencer Wells, F Mark L Charnock, Trivadi S Ganesan

The human L-threonine 3-dehydrogenase gene is an expressed pseudogene

Alasdair J Edgar

Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight

Alex Doney, Bettina Fischer, David Frew, Alastair Cumming, David M Flavell, Michael World, Hugh E Montgomery, Douglas Boyle, Andrew Morris, Colin NA Palmer

Chromosomal aberrations in patients with head and neck squamous cell carcinoma do not vary based on severity of tobacco/alcohol exposure

Bhuvanesh Singh, Volkert B Wreesmann, David Pfister, Ashok Poluri, Ashok R Shaha, Dennis Kraus, Jatin P Shah, Pulivarthi H Rao

Inferring relationships between pairs of individuals from locus heterozygosities

Silvano Presciuttini, Chiara Toni, Elena Tempestini, Simonetta Verdiani, Lucia Casarino, Isabella Spinetti, Francesco De Stefano, Ranieri Domenici, Joan E Bailey-Wilson

Human CCS gene: genomic organization and exclusion as a candidate for amyotrophic lateral sclerosis (ALS)

Asli N Silahtaroglu, Karen Brondum-Nielsen, Ole Gredal, Lene Werdelin, Marios Panas, Michael B Petersen, Niels Tommerup, Zeynep Tümer

Telomere formation on macronuclear chromosomes of Oxytricha trifallax and O. fallax: alternatively processed regions have multiple telomere addition sites

Kevin R Williams, Thomas G Doak, Glenn Herrick

Conservation of the COP9/signalosome in budding yeast

Susan Wee, Bettina Hetfeld, Wolfgang Dubiel, Dieter A Wolf

Comparative transcription map of the wobbler critical region on mouse chromosome 11 and the homologous region on human chromosome 2p13-14

Sonja Fuchs, Karin Resch, Cora Thiel, Michael Ulbrich, Matthias Platzer, Harald Jockusch, Thomas Schmitt-John

Setting of graded levels of a protein in yeast by a t-degron technique as applied to phosphoglycerate mutase

Katja Heidrich, Dan G Fraenkel

Screening of the arrestin gene in dogs afflicted with generalized progressive retinal atrophy

Gabriele Dekomien, J？rg Thomas Epplen

A hierarchical statistical model for estimating population properties of quantitative genes

Samuel S Wu, Chang-Xing Ma, Rongling Wu, George Casella

The Tnfrh1 (Tnfrsf23) gene is weakly imprinted in several organs and expressed at the trophoblast-decidua interface

Lorraine Clark, Michelle Wei, Giorgio Cattoretti, Cathy Mendelsohn, Benjamin Tycko

Identification and preliminary characterization of mouse Adam33

Teresa M Gunn, Arezou Azarani, Philip H Kim, Richard W Hyman, Ronald W Davis, Gregory S Barsh

The minisequencing method: a simple strategy for genetic screening of MEN 2 families

Maria Jo？o Bugalho, Rita Domingues, Luís Sobrinho

Statistics on continuous IBD data: Exact distribution evaluation for a pair of full(half)-sibs and a pair of a (great-) grandchild with a (great-) grandparent

Valeri T Stefanov

Occurrence of leu+ revertants under starvation cultures in Escherichia coli is growth-dependent

Jianling Jin, Peiji Gao, Yumin Mao

Isolation and characterization of new Saccharomyces cerevisiae mutants perturbed in nuclear pore complex assembly

Kathryn J Ryan, Susan R Wente

Analysis of genetic heterogeneity in the HCAR adenovirus-binding Ig1 domain in a Caucasian Flemish population

Inge Thoelen, Griet Duson, Elke Wollants, Marc Van Ranst

SNP frequency, haplotype structure and linkage disequilibrium in elite maize inbred lines

Ada Ching, Katherine S Caldwell, Mark Jung, Maurine Dolan, Oscar Smith, Scott Tingey, Michele Morgante, Antoni J Rafalski

Apolipoprotein C3 SstI polymorphism and triglyceride levels in Asian Indians

S Chhabra, R Narang, LR Krishnan, S Vasisht, DP Agarwal, LM Srivastava, SC Manchanda, N Das

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

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

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

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

RHD positive haplotypes in D negative Europeans

Franz F Wagner, Alexander Frohmajer, Willy A Flegel

Gene targeting in mosquito cells: a demonstration of 'knockout' technology in extrachromosomal gene arrays

Paul Eggleston, Yuguang Zhao

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

Isozyme and allozyme markers distinguishing two morphologically similar, medically important Mastomys species (Rodentia: Muridae)

Andre A Smit, Herman FH Van der Bank

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

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

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

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

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

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

A sensitive and rapid assay for homologous recombination in mosquito cells: impact of vector topology and implications for gene targeting

Paul Eggleston, Yuguang Zhao

©2008-2020 OALib, Inc | Public user content licensed CC-BY 4.0 unless otherwise specified. OALib ISSN Online: 2333-9721 OALib ISSN Print: 2333-9705