Tuesday, 30 March 2010

What's new for 'JKB_daily1' in PubMed

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Sender's message: Sepsis or genomics or altitude: JKB_daily1

Sent on Tuesday, 2010 Mar 30
Search (sepsis[MeSH Terms] OR septic shock[MeSH Terms] OR altitude[MeSH Terms] OR genomics[MeSH Terms] OR genetics[MeSH Terms] OR retrotransposons[MeSH Terms] OR macrophage[MeSH Terms]) AND ("2009/8/8"[Publication Date] : "3000"[Publication Date]) AND (("Science"[Journal] OR "Nature"[Journal] OR "The New England journal of medicine"[Journal] OR "Lancet"[Journal] OR "Nature genetics"[Journal] OR "Nature medicine"[Journal]) OR (Hume DA[Author] OR Baillie JK[Author] OR Faulkner, Geoffrey J[Author]))
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PubMed Results
Items 1 - 6 of 6

1. Nature. 2010 Feb 18;463(7283):943-7.

Complete Khoisan and Bantu genomes from southern Africa.

Schuster SC, Miller W, Ratan A, Tomsho LP, Giardine B, Kasson LR, Harris RS, Petersen DC, Zhao F, Qi J, Alkan C, Kidd JM, Sun Y, Drautz DI, Bouffard P, Muzny DM, Reid JG, Nazareth LV, Wang Q, Burhans R, Riemer C, Wittekindt NE, Moorjani P, Tindall EA, Danko CG, Teo WS, Buboltz AM, Zhang Z, Ma Q, Oosthuysen A, Steenkamp AW, Oostuisen H, Venter P, Gajewski J, Zhang Y, Pugh BF, Makova KD, Nekrutenko A, Mardis ER, Patterson N, Pringle TH, Chiaromonte F, Mullikin JC, Eichler EE, Hardison RC, Gibbs RA, Harkins TT, Hayes VM.

Pennsylvania State University, Center for Comparative Genomics and Bioinformatics, 310 Wartik Lab, University Park, Pennsylvania 16802, USA. scs@bx.psu.edu

Comment in:

The genetic structure of the indigenous hunter-gatherer peoples of southern Africa, the oldest known lineage of modern human, is important for understanding human diversity. Studies based on mitochondrial and small sets of nuclear markers have shown that these hunter-gatherers, known as Khoisan, San, or Bushmen, are genetically divergent from other humans. However, until now, fully sequenced human genomes have been limited to recently diverged populations. Here we present the complete genome sequences of an indigenous hunter-gatherer from the Kalahari Desert and a Bantu from southern Africa, as well as protein-coding regions from an additional three hunter-gatherers from disparate regions of the Kalahari. We characterize the extent of whole-genome and exome diversity among the five men, reporting 1.3 million novel DNA differences genome-wide, including 13,146 novel amino acid variants. In terms of nucleotide substitutions, the Bushmen seem to be, on average, more different from each other than, for example, a European and an Asian. Observed genomic differences between the hunter-gatherers and others may help to pinpoint genetic adaptations to an agricultural lifestyle. Adding the described variants to current databases will facilitate inclusion of southern Africans in medical research efforts, particularly when family and medical histories can be correlated with genome-wide data.

PMID: 20164927 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH Terms:

  • African Continental Ancestry Group/genetics*
  • Asian Continental Ancestry Group/genetics
  • Ethnic Groups/genetics*
  • European Continental Ancestry Group/genetics
  • Exons/genetics
  • Genetics, Medical
  • Genome, Human/genetics*
  • Humans
  • Phylogeny
  • Polymorphism, Single Nucleotide/genetics
  • South Africa/ethnology

Secondary Source ID:

  • GEO/GSE19048

Grant Support:

  • R01GM087472/GM/NIGMS NIH HHS/United States
2. Nature. 2010 Feb 18;463(7283):899-905.

The landscape of somatic copy-number alteration across human cancers.

Beroukhim R, Mermel CH, Porter D, Wei G, Raychaudhuri S, Donovan J, Barretina J, Boehm JS, Dobson J, Urashima M, Mc Henry KT, Pinchback RM, Ligon AH, Cho YJ, Haery L, Greulich H, Reich M, Winckler W, Lawrence MS, Weir BA, Tanaka KE, Chiang DY, Bass AJ, Loo A, Hoffman C, Prensner J, Liefeld T, Gao Q, Yecies D, Signoretti S, Maher E, Kaye FJ, Sasaki H, Tepper JE, Fletcher JA, Tabernero J, Baselga J, Tsao MS, Demichelis F, Rubin MA, Janne PA, Daly MJ, Nucera C, Levine RL, Ebert BL, Gabriel S, Rustgi AK, Antonescu CR, Ladanyi M, Letai A, Garraway LA, Loda M, Beer DG, True LD, Okamoto A, Pomeroy SL, Singer S, Golub TR, Lander ES, Getz G, Sellers WR, Meyerson M.

Cancer Program and Medical and Population Genetics Group, The Broad Institute of M.I.T. and Harvard, 7 Cambridge Center.

A powerful way to discover key genes with causal roles in oncogenesis is to identify genomic regions that undergo frequent alteration in human cancers. Here we present high-resolution analyses of somatic copy-number alterations (SCNAs) from 3,131 cancer specimens, belonging largely to 26 histological types. We identify 158 regions of focal SCNA that are altered at significant frequency across several cancer types, of which 122 cannot be explained by the presence of a known cancer target gene located within these regions. Several gene families are enriched among these regions of focal SCNA, including the BCL2 family of apoptosis regulators and the NF-kappaBeta pathway. We show that cancer cells containing amplifications surrounding the MCL1 and BCL2L1 anti-apoptotic genes depend on the expression of these genes for survival. Finally, we demonstrate that a large majority of SCNAs identified in individual cancer types are present in several cancer types.

PMCID: PMC2826709 [Available on 2010/8/18]

PMID: 20164920 [PubMed - indexed for MEDLINE]
Related articles
Click here to read

Publication Types:

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH Terms:

  • Apoptosis/genetics
  • Cell Line, Tumor
  • Cell Survival/genetics
  • DNA Copy Number Variations/genetics*
  • Gene Amplification/genetics
  • Gene Dosage/genetics*
  • Genomics
  • Humans
  • Multigene Family/genetics
  • Neoplasms/classification
  • Neoplasms/genetics*
  • Neoplasms/pathology
  • Proto-Oncogene Proteins c-bcl-2/genetics
  • Signal Transduction
  • bcl-X Protein/genetics

Substances:

  • BCL2L1 protein, human
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-X Protein
  • myeloid cell leukemia sequence 1 protein

Secondary Source ID:

  • GEO/GSE19399

Grant Support:

  • K08CA122833/CA/NCI NIH HHS/United States
  • P01CA 098101/CA/NCI NIH HHS/United States
  • P01CA085859/CA/NCI NIH HHS/United States
  • P50CA90578/CA/NCI NIH HHS/United States
  • R01CA109038/CA/NCI NIH HHS/United States
  • R01CA109467/CA/NCI NIH HHS/United States
  • Howard Hughes Medical Institute/United States
3. Nature. 2010 Feb 18;463(7283):877.

Outcry stopped approved pig study of avalanche survival.

Brugger H, Paal P, Falk M.
PMID: 20164903 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Letter

MeSH Terms:

  • Altitude
  • Anesthesia
  • Animal Experimentation/standards
  • Animal Rights*
  • Animals
  • Avalanches*
  • Disasters*
  • Europe
  • Models, Animal*
  • Public Opinion*
  • Snow
  • Survival/physiology*
  • Swine/physiology*
4. Nature. 2010 Feb 18;463(7283):859.

Genomics firms turn to other markets.

Hayden EC.
PMID: 20164890 [PubMed - indexed for MEDLINE]
Related articles
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Publication Types:

  • News

MeSH Terms:

  • Costs and Cost Analysis
  • Genome, Human
  • Genomics/economics*
  • Genomics/instrumentation
  • Genomics/trends*
  • Humans
  • Rhodopseudomonas/genetics
  • Rhodopseudomonas/metabolism
  • Sequence Analysis, DNA/economics*
  • Sequence Analysis, DNA/instrumentation
  • Sequence Analysis, DNA/trends*
5. Nature. 2010 Feb 18;463(7283):858.

How accurate are cancer cell lines?

Borrell B.
PMID: 20164888 [PubMed - indexed for MEDLINE]
Related articles
Click here to read

Publication Types:

  • News

MeSH Terms:

  • Cell Line, Tumor/metabolism*
  • Genetics, Medical/methods*
  • Genetics, Medical/trends*
  • Genomics/methods*
  • Genomics/trends*
  • Humans
  • Neoplasms/genetics*
  • Neoplasms/pathology*
  • Reproducibility of Results
  • Sequence Analysis, DNA/trends
6. Nature. 2010 Feb 18;463(7283):857.

Africa yields two full human genomes.

Ledford H.

Comment on:

PMID: 20164887 [PubMed - indexed for MEDLINE]
Related articles
Click here to read

Publication Types:

  • Comment
  • News

MeSH Terms:

  • African Continental Ancestry Group/genetics*
  • Ethnic Groups/genetics*
  • Genetic Variation/genetics
  • Genome, Human/genetics*
  • Genomics*/trends
  • Humans
  • Malaria, Vivax/genetics
  • Male
  • Minority Groups
  • Phylogeny
  • South Africa/ethnology

Wednesday, 24 March 2010

What's new for 'JKB_daily1' in PubMed

This message contains My NCBI what's new results from the National Center for Biotechnology Information (NCBI) at the U.S. National Library of Medicine (NLM).
Do not reply directly to this message.

Sender's message: Sepsis or genomics or altitude: JKB_daily1

Sent on Wednesday, 2010 Mar 24
Search (sepsis[MeSH Terms] OR septic shock[MeSH Terms] OR altitude[MeSH Terms] OR genomics[MeSH Terms] OR genetics[MeSH Terms] OR retrotransposons[MeSH Terms] OR macrophage[MeSH Terms]) AND ("2009/8/8"[Publication Date] : "3000"[Publication Date]) AND (("Science"[Journal] OR "Nature"[Journal] OR "The New England journal of medicine"[Journal] OR "Lancet"[Journal] OR "Nature genetics"[Journal] OR "Nature medicine"[Journal]) OR (Hume DA[Author] OR Baillie JK[Author] OR Faulkner, Geoffrey J[Author]))
Click here to view complete results in PubMed. (Results may change over time.)
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PubMed Results
Items 1 - 5 of 5

1. Nature. 2010 Feb 11;463(7282):763-8.

Genome sequencing and analysis of the model grass Brachypodium distachyon.

International Brachypodium Initiative.

Collaborators: Vogel JP, Garvin DF, Mockler TC, Schmutz J, Rokhsar D, Bevan MW, Barry K, Lucas S, Harmon-Smith M, Lail K, Tice H, Schmutz J, Grimwood J, McKenzie N, Bevan MW, Huo N, Gu YQ, Lazo GR, Anderson OD, Vogel JP, You FM, Luo MC, Dvorak J, Wright J, Febrer M, Bevan MW, Idziak D, Hasterok R, Garvin DF, Lindquist E, Wang M, Fox SE, Priest HD, Filichkin SA, Givan SA, Bryant DW, Chang JH, Mockler TC, Wu H, Wu W, Hsia AP, Schnable PS, Kalyanaraman A, Barbazuk B, Michael TP, Hazen SP, Bragg JN, Laudencia-Chingcuanco D, Vogel JP, Garvin DF, Weng Y, McKenzie N, Bevan MW, Haberer G, Spannagl M, Mayer K, Rattei T, Mitros T, Rokhsar D, Lee SJ, Rose JK, Mueller LA, York TL, Wicker T, Buchmann JP, Tanskanen J, Schulman AH, Gundlach H, Wright J, Bevan M, de Oliveira AC, Maia Lda C, Belknap W, Gu YQ, Jiang N, Lai J, Zhu L, Ma J, Sun C, Pritham E, Salse J, Murat F, Abrouk M, Haberer G, Spannagl M, Mayer K, Bruggmann R, Messing J, You FM, Luo MC, Dvorak J, Fahlgren N, Fox SE, Sullivan CM, Mockler TC, Carrington JC, Chapman EJ, May GD, Zhai J, Ganssmann M, Gurazada SG, German M, Meyers BC, Green PJ, Bragg JN, Tyler L, Wu J, Gu YQ, Lazo GR, Laudencia-Chingcuanco D, Thomson J, Vogel JP, Hazen SP, Chen S, Scheller HV, Harholt J, Ulvskov P, Fox SE, Filichkin SA, Fahlgren N, Kimbrel JA, Chang JH, Sullivan CM, Chapman EJ, Carrington JC, Mockler TC, Bartley LE, Cao P, Jung KH, Sharma MK, Vega-Sanchez M, Ronald P, Dardick CD, De Bodt S, Verelst W, Inzé D, Heese M, Schnittger A, Yang X, Kalluri UC, Tuskan GA, Hua Z, Vierstra RD, Garvin DF, Cui Y, Ouyang S, Sun Q, Liu Z, Yilmaz A, Grotewold E, Sibout R, Hematy K, Mouille G, Höfte H, Michael T, Pelloux J, O'Connor D, Schnable J, Rowe S, Harmon F, Cass CL, Sedbrook JC, Byrne ME, Walsh S, Higgins J, Bevan M, Li P, Brutnell T, Unver T, Budak H, Belcram H, Charles M, Chalhoub B, Baxter I.

USDA-ARS Western Regional Research Center, Albany, California 94710, USA.

Three subfamilies of grasses, the Ehrhartoideae, Panicoideae and Pooideae, provide the bulk of human nutrition and are poised to become major sources of renewable energy. Here we describe the genome sequence of the wild grass Brachypodium distachyon (Brachypodium), which is, to our knowledge, the first member of the Pooideae subfamily to be sequenced. Comparison of the Brachypodium, rice and sorghum genomes shows a precise history of genome evolution across a broad diversity of the grasses, and establishes a template for analysis of the large genomes of economically important pooid grasses such as wheat. The high-quality genome sequence, coupled with ease of cultivation and transformation, small size and rapid life cycle, will help Brachypodium reach its potential as an important model system for developing new energy and food crops.

PMID: 20148030 [PubMed - indexed for MEDLINE]
Related articles
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Publication Types:

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH Terms:

  • Chromosomes, Plant/genetics
  • Crops, Agricultural/genetics
  • DNA Transposable Elements/genetics
  • Evolution, Molecular
  • Gene Fusion/genetics
  • Genes, Plant/genetics
  • Genome, Plant/genetics*
  • Genomics
  • Molecular Sequence Data
  • Oryza sativa/genetics
  • Poaceae/classification
  • Poaceae/genetics*
  • RNA, Plant/analysis
  • RNA, Plant/genetics
  • Sequence Analysis, DNA
  • Sorghum/genetics
  • Synteny/genetics
  • Transcription, Genetic/genetics

Substances:

  • DNA Transposable Elements
  • RNA, Plant

Secondary Source ID:

  • GENBANK/GT758162
  • GENBANK/GT758163
  • GENBANK/GT758164
  • GENBANK/GT758165
  • GENBANK/GT758166
  • GENBANK/GT758167
  • GENBANK/GT758168
  • GENBANK/GT758169
  • GENBANK/GT758170
  • GENBANK/GT758171
  • GENBANK/GT758172
  • GENBANK/GT758173
  • GENBANK/GT758174
  • GENBANK/GT758175
  • GENBANK/GT758176
  • GENBANK/GT758177
  • GENBANK/GT758178
  • GENBANK/GT758179
  • GENBANK/GT758180
  • GENBANK/GT758181
  • GENBANK/GT758182
  • GENBANK/GT758183
  • GENBANK/GT758184
  • GENBANK/GT758185
  • GENBANK/GT758186
  • GENBANK/GT758187
  • GENBANK/GT758188
  • GENBANK/GT758189
  • GENBANK/GT758190
  • GENBANK/GT758191
  • GENBANK/GT758192
  • GENBANK/GT758193
  • GENBANK/GT758194
  • GENBANK/GT758195
  • GENBANK/GT758196
  • GENBANK/GT758197
  • GENBANK/GT758198
  • GENBANK/GT758 199
  • GENBANK/GT758200
  • GENBANK/GT758201
  • GENBANK/GT758202
  • GENBANK/GT758203
  • GENBANK/GT758204
  • GENBANK/GT758205
  • GENBANK/GT758206
  • GENBANK/GT758207
  • GENBANK/GT758208
  • GENBANK/GT758209
  • GENBANK/GT758210
  • GENBANK/GT758211
  • GENBANK/GT758212
  • GENBANK/GT758213
  • GENBANK/GT758214
  • GENBANK/GT758215
  • GENBANK/GT758216
  • GENBANK/GT758217
  • GENBANK/GT758218
  • GENBANK/GT758219
  • GENBANK/GT758220
  • GENBANK/GT758221
  • GENBANK/GT758222
  • GENBANK/GT758223
  • GENBANK/GT758224
  • GENBANK/GT758225
  • GENBANK/GT758226
  • GENBANK/GT758227
  • GENBANK/GT758228
  • GENBANK/GT758229
  • GENBANK/GT758230
  • GENBANK/GT758231
  • GENBANK/GT758232
  • GENBANK/GT758233
  • GENBANK/GT758234
  • GENBANK/GT758235
  • GENBANK/GT758236
  • GENBANK/GT758237
  • GENBANK/GT758238
  • GE NBANK/GT758239
  • GENBANK/GT758240
  • GENBANK/GT758241
  • GENBANK/GT758242
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  • GENBANK/GT758280
  • GENBANK/GT758281
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  • GENBANK/GT758283
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  • GENBANK/GT758285
  • GENBANK/GT758286
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  • GENBANK/GT758310
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  • GENBANK/GT758314
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  • GENBA NK/GT758318
  • GENBANK/GT758319
  • GENBANK/GT758320
  • GENBANK/GT758321
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  • GENBANK/GT758323
  • GENBANK/GT758324
  • GENBANK/GT758325
  • GENBANK/GT758326
  • GENBANK/GT758327
  • GENBANK/GT758328
  • GENBANK/GT758329
  • GENBANK/GT758330
  • GENBANK/GT758331
  • GENBANK/GT758332
  • GENBANK/GT758333
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  • GENBANK/GT758335
  • GENBANK/GT758336
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  • GENBANK/GT758339
  • GENBANK/GT758340
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Grant Support:

  • Biotechnology and Biological Sciences Research Council/United Kingdom
2. Nature. 2010 Feb 11;463(7282):757-62.

Ancient human genome sequence of an extinct Palaeo-Eskimo.

Rasmussen M, Li Y, Lindgreen S, Pedersen JS, Albrechtsen A, Moltke I, Metspalu M, Metspalu E, Kivisild T, Gupta R, Bertalan M, Nielsen K, Gilbert MT, Wang Y, Raghavan M, Campos PF, Kamp HM, Wilson AS, Gledhill A, Tridico S, Bunce M, Lorenzen ED, Binladen J, Guo X, Zhao J, Zhang X, Zhang H, Li Z, Chen M, Orlando L, Kristiansen K, Bak M, Tommerup N, Bendixen C, Pierre TL, Grønnow B, Meldgaard M, Andreasen C, Fedorova SA, Osipova LP, Higham TF, Ramsey CB, Hansen TV, Nielsen FC, Crawford MH, Brunak S, Sicheritz-Pontén T, Villems R, Nielsen R, Krogh A, Wang J, Willerslev E.

Centre for GeoGenetics, Natural History Museum of Denmark and Department of Biology, University of Copenhagen, Universitetsparken 15, DK-2100 Copenhagen, Denmark.

Comment in:

We report here the genome sequence of an ancient human. Obtained from approximately 4,000-year-old permafrost-preserved hair, the genome represents a male individual from the first known culture to settle in Greenland. Sequenced to an average depth of 20x, we recover 79% of the diploid genome, an amount close to the practical limit of current sequencing technologies. We identify 353,151 high-confidence single-nucleotide polymorphisms (SNPs), of which 6.8% have not been reported previously. We estimate raw read contamination to be no higher than 0.8%. We use functional SNP assessment to assign possible phenotypic characteristics of the individual that belonged to a culture whose location has yielded only trace human remains. We compare the high-confidence SNPs to those of contemporary populations to find the populations most closely related to the individual. This provides evidence for a migration from Siberia into the New World some 5,500 years ago, independent of that giving rise to the modern Native Americans and Inuit.

PMID: 20148029 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Historical Article
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH Terms:

  • Cryopreservation*
  • Emigration and Immigration/history
  • Extinction, Biological*
  • Genetics, Population
  • Genome, Human/genetics*
  • Genomics
  • Genotype
  • Greenland
  • Hair
  • History, Ancient
  • Humans
  • Inuits/genetics*
  • Male
  • Phenotype
  • Phylogeny
  • Polymorphism, Single Nucleotide/genetics
  • Sequence Analysis, DNA
  • Siberia/ethnology
3. Nature. 2010 Feb 11;463(7282):739-40.

Evolutionary biology: Face of the past reconstructed.

Lambert DM, Huynen L.

Comment on:

PMID: 20148020 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Comment
  • Historical Article
  • News

MeSH Terms:

  • Animals
  • Cryopreservation*
  • Emigration and Immigration/history
  • Genome, Human/genetics*
  • Genomics
  • Greenland
  • Hair/metabolism
  • History, Ancient
  • Humans
  • Inuits/genetics*
  • Male
  • Phenotype
  • Phylogeny*
  • Polymorphism, Single Nucleotide/genetics
  • Siberia/ethnology
4. Nature. 2010 Feb 11;463(7282):724-5.

Palaeogenetics: Icy resolve.

Dalton R.
PMID: 20148008 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Biography
  • Historical Article
  • News
  • Portraits

MeSH Terms:

  • Animals
  • Arctic Regions
  • Cryopreservation
  • DNA/genetics
  • DNA/isolation & purification
  • DNA, Mitochondrial/analysis
  • DNA, Mitochondrial/genetics
  • Denmark
  • Emigration and Immigration/history*
  • Feces
  • Fossils
  • Genetics, Medical/history
  • Genome, Human/genetics*
  • Greenland/ethnology
  • History, 20th Century
  • History, 21st Century
  • History, Ancient
  • Humans
  • Inuits/ethnology*
  • Inuits/history*
  • Male
  • Paleontology/history*
  • Phylogeny
  • Reproducibility of Results
  • Sequence Analysis, DNA
  • Siberia/ethnology

Substances:

  • DNA, Mitochondrial
  • DNA

Personal Name as Subject:

  • Willerslev E
5. Lancet. 2010 Mar 6;375(9717):834-45. Epub 2010 Feb 2.

Diagnostic value of clinical features at presentation to identify serious infection in children in developed countries: a systematic review.

Van den Bruel A, Haj-Hassan T, Thompson M, Buntinx F, Mant D; European Research Network on Recognising Serious Infection investigators.

Collaborators: Van den Bruel A, Thompson M, Buntinx F, Mant D, Haj-Hassan T, Oostenbrink R, Moll H, Aertgeerts B, Lakhanpaul M.

Department of General Practice, Katholieke Universiteit Leuven, Leuven, Belgium. ann.vandenbruel@med.kuleuven.be

Comment in:

BACKGROUND: Our aim was to identify which clinical features have value in confirming or excluding the possibility of serious infection in children presenting to ambulatory care settings in developed countries. METHODS: In this systematic review, we searched electronic databases (Medline, Embase, DARE, CINAHL), reference lists of relevant studies, and contacted experts to identify articles assessing clinical features of serious infection in children. 1939 potentially relevant studies were identified. Studies were selected on the basis of six criteria: design (studies of diagnostic accuracy or prediction rules), participants (otherwise healthy children aged 1 month to 18 years), setting (ambulatory care), outcome (serious infection), features assessed (assessable in ambulatory care setting), and sufficient data reported. Quality assessment was based on the Quality Assessment of Diagnostic Accuracy Studies criteria. We calculated likelihood ratios for the presence (positive likelihood ratio) or absence (negative likelihood ratio) of each clinical feature and pre-test and post-test probabilities of the outcome. Clinical features with a positive likelihood ratio of more than 5.0 were deemed red flags (ie, warning signs for serious infection); features with a negative likelihood ratio of less than 0.2 were deemed rule-out signs. FINDINGS: 30 studies were included in the analysis. Cyanosis (positive likelihood ratio range 2.66-52.20), rapid breathing (1.26-9.78), poor peripheral perfusion (2.39-38.80), and petechial rash (6.18-83.70) were identified as red flags in several studies. Parental concern (positive likelihood ratio 14.40, 95% CI 9.30-22.10) and clinician instinct (positive likelihood ratio 23.50, 95 % CI 16.80-32.70) were identified as strong red flags in one primary care study. Temperature of 40 degrees C or more has value as a red flag in settings with a low prevalence of serious infection. No single clinical feature has rule-out value but some combinations can be used to exclude the possibility of serious infection-for example, pneumonia is very unlikely (negative likelihood ratio 0.07, 95% CI 0.01-0.46) if the child is not short of breath and there is no parental concern. The Yale Observation Scale had little value in confirming (positive likelihood ratio range 1.10-6.70) or excluding (negative likelihood ratio range 0.16-0.97) the possibility of serious infection. INTERPRETATION: The red flags for serious infection that we identified should be used routinely, but serious illness will still be missed without effective use of precautionary measures. We now need to identify the level of risk at which clinical action should be taken. FUNDING: Health Technology Assessment and National Institute for Health Research National School for Primary Care Research. Copyright 2010 Elsevier Ltd. All rights reserved.

PMID: 20132979 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't
  • Review

MeSH Terms:

  • Acute Disease
  • Ambulatory Care*
  • Bacteremia/diagnosis
  • Child
  • Dehydration/diagnosis
  • Dehydration/etiology
  • Developed Countries*
  • Gastroenteritis/diagnosis
  • Humans
  • Infection/diagnosis*
  • Meningitis/diagnosis
  • Meningococcal Infections/diagnosis
  • Pneumonia/diagnosis
  • Primary Health Care

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PubMed Results
Items 1 - 2 of 2

1. N Engl J Med. 2010 Mar 11;362(10):942-3.

Toward a personalized treatment of Hodgkin's disease.

DeVita VT Jr, Costa J.

Comment on:

PMID: 20220189 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Comment
  • Editorial

MeSH Terms:

  • Antigens, CD/analysis*
  • Antigens, Differentiation, Myelomonocytic/analysis*
  • Disease-Free Survival
  • Gene Expression Profiling
  • Hodgkin Disease/genetics*
  • Hodgkin Disease/therapy
  • Humans
  • Macrophages*/immunology
  • Prognosis
  • Reed-Sternberg Cells/pathology

Substances:

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD68 antigen, human
2. N Engl J Med. 2010 Mar 11;362(10):875-85.

Tumor-associated macrophages and survival in classic Hodgkin's lymphoma.

Steidl C, Lee T, Shah SP, Farinha P, Han G, Nayar T, Delaney A, Jones SJ, Iqbal J, Weisenburger DD, Bast MA, Rosenwald A, Muller-Hermelink HK, Rimsza LM, Campo E, Delabie J, Braziel RM, Cook JR, Tubbs RR, Jaffe ES, Lenz G, Connors JM, Staudt LM, Chan WC, Gascoyne RD.

Department of Pathology and Laboratory Medicine, British Columbia Cancer Agency, Vancouver, BC, Canada.

Comment in:

BACKGROUND: Despite advances in treatments for Hodgkin's lymphoma, about 20% of patients still die from progressive disease. Current prognostic models predict the outcome of treatment with imperfect accuracy, and clinically relevant biomarkers have not been established to improve on the International Prognostic Score. METHODS: Using gene-expression profiling, we analyzed 130 frozen samples obtained from patients with classic Hodgkin's lymphoma during diagnostic lymph-node biopsy to determine which cellular signatures were correlated with treatment outcome. We confirmed our findings in an independent cohort of 166 patients, using immunohistochemical analysis. RESULTS: Gene-expression profiling identified a gene signature of tumor-associated macrophages that was significantly associated with primary treatment failure (P=0.02). In an independent cohort of patients, we found that an increased number of CD68+ macrophages was correlated with a shortened progression-free survival (P=0.03) and with an increased likelihood of relapse after autologous hematopoietic stem-cell transplantation (P=0.008), resulting in shortened disease-specific survival (P=0.003). In multivariate analysis, this adverse prognostic factor outperformed the International Prognostic Score for disease-specific survival (P=0.003 vs. P=0.03). The absence of an elevated number of CD68+ cells in patients with limited-stage disease defined a subgroup of patients with a long-term disease-specific survival of 100% with the use of current treatment strategies. CONCLUSIONS: An increased number of tumor-associated macrophages was strongly associated with shortened survival in patients with classic Hodgkin's lymphoma and provides a new biomarker for risk stratification. 2010 Massachusetts Medical Society

PMID: 20220182 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH Terms:

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Analysis of Variance
  • Antigens, CD/analysis*
  • Antigens, Differentiation, Myelomonocytic/analysis*
  • Child
  • Disease-Free Survival
  • Female
  • Gene Expression
  • Gene Expression Profiling*
  • Gene Expression Regulation, Neoplastic
  • Hodgkin Disease/genetics*
  • Hodgkin Disease/mortality
  • Hodgkin Disease/pathology
  • Humans
  • Immunohistochemistry
  • Kaplan-Meiers Estimate
  • Lymph Nodes/pathology*
  • Macrophages*/immunology
  • Male
  • Middle Aged
  • Neoplasm Staging
  • Prognosis
  • RNA, Neoplasm/analysis
  • Reed-Sternberg Cells/pathology
  • Survival Rate
  • Treatment Failure
  • Tumor Markers, Biological/analysis
  • Tumor Markers, Biological/genetics
  • Young Adult

Substances:

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD68 antigen, human
  • RNA, Neoplasm
  • Tumor Markers, Biological

Grant Support:

  • 178536/Canadian Institutes of Health Research/Canada
  • U01-CA 114778/CA/NCI NIH HHS/United States
  • U01-CA114778-01/CA/NCI NIH HHS/United States