Mouse models of atherosclerosis: explaining critical roles of lipid metabolism and inflammation.

Abstract:

:Atherosclerosis is the most common cause of death globally. It is a complex disease involving morphological and cellular changes in vascular walls. Studying molecular mechanism of the disease is hindered by disease complexity and lack of robust noninvasive diagnostics in human. Mouse models are the most popular animal models that allow researchers to study the mechanism of disease progression. In this review we discuss the advantage and development of mouse as a model for atherosclerotic research. Along with commonly used models, this review discusses strains that are used to study the role of two critical processes associated with the disease-lipid metabolism and inflammation.

journal_name

J Appl Genet

authors

Mukhopadhyay R

doi

10.1007/s13353-013-0134-4

subject

Has Abstract

pub_date

2013-05-01 00:00:00

pages

185-92

issue

2

eissn

1234-1983

issn

2190-3883

journal_volume

54

pub_type

杂志文章,评审
  • Association between single-nucleotide polymorphisms of selected genes involved in the response to DNA damage and risk of colon, head and neck, and breast cancers in a Polish population.

    abstract::Single-nucleotide polymorphisms in genes involved in DNA-damage-induced responses are reported frequently to be a risk factor in various cancer types. Here we analysed polymorphisms in 5 genes involved in DNA repair (XPD Asp312Asn and Lys751Gln, XRCC1 Arg399Gln, APE1 Asp148Glu, NBS1 Glu185Gln, and XPA G-4A) and in a g...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03208865

    authors: Jelonek K,Gdowicz-Klosok A,Pietrowska M,Borkowska M,Korfanty J,Rzeszowska-Wolny J,Widlak P

    更新日期:2010-01-01 00:00:00

  • The current state of xenotransplantation.

    abstract::Pigs as a source of grafts for xenotransplantation can help to overcome the rapidly growing shortage of human donors. However, in the case of pig-to-human transplantation, the antibody-xenoantigen complexes lead to the complement activation and immediate hyperacute rejection. Methods eliminating hyperacute rejection (...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章,评审

    doi:10.1007/s13353-014-0261-6

    authors: Zeyland J,Lipiński D,Słomski R

    更新日期:2015-05-01 00:00:00

  • Genetic determination of variability of barley doubled haploids inoculated with Fusarium culmorum (W.G.Sm.) Sacc. with regard to mycotoxin accumulation and reduction in yield traits.

    abstract::The genetic determination of variability of barley doubled haploid (DH) lines in regard of their susceptibility to Fusarium head blight caused by Fusarium culmorum was studied. The susceptibility was evaluated in 3-year field experiment on the basis of reduction in yield traits and myotoxin accumulation in infected ke...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:

    authors: Surma M,Adamski T,Chełkowski J,Goliński P,Kaczmarek Z,Kostecki M,Perkowski J,Wiśniewska H

    更新日期:2000-01-01 00:00:00

  • CCAAT/enhancer binding protein-beta negatively regulates the expression of glycerol-3-phosphate dehydrogenase 1 in pig PK-15 cells.

    abstract::Soluble glycerol-3-phosphate dehydrogenase 1 (GPD1, EC 1.1.1.8) plays important roles in the synthesis of triacylglycerol and in the glycerol-3-phosphate shutter. Though GPD1 is expressed in most adult tissues, little is known about the regulation of its expression. In this study, we analyzed the characters, organizat...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-011-0050-4

    authors: Gao Y,Pan Y

    更新日期:2011-11-01 00:00:00

  • A novel genotype c.1228C>G/c.1448C-1498C (L371V/Rec-NciI) in a 3-year-old child with type 1 Gaucher disease.

    abstract::Gaucher disease (GD) is an autosomal recessive inborn error of metabolism, resulting from a deficiency of the enzyme glucocerebrosidase, causing an accumulation of the glycolipid glucocerebroside within lysosomes of macrophages in the reticuloendothelial system. Three major clinical forms have been assigned and more t...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03195642

    authors: Yassin NA,Muwakkit SA,Ibrahim AO,Kayim IM,Habbal MZ,Chamseddine NM,Musallam KM,Shamseddine AI

    更新日期:2008-01-01 00:00:00

  • Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency.

    abstract::The role of genetic background in childhood-onset combined pituitary hormone deficiency (CPHD) has been extensively studied. The major contributors are the PROP1, POU1F1, LHX3, LHX4 and HESX1 genes coding transcription factors implicated in pituitary organogenesis. The clinical consequences of mutations encompass impa...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-015-0328-z

    authors: Ziemnicka K,Budny B,Drobnik K,Baszko-Błaszyk D,Stajgis M,Katulska K,Waśko R,Wrotkowska E,Słomski R,Ruchała M

    更新日期:2016-08-01 00:00:00

  • Molecular mapping of powdery mildew resistance gene Eg-3 in cultivated oat (Avena sativa L. cv. Rollo).

    abstract::Powdery mildew is a prevalent fungal disease affecting oat (Avena sativa L.) production in Europe. Common oat cultivar Rollo was previously shown to carry the powdery mildew resistance gene Eg-3 in common with cultivar Mostyn. The resistance gene was mapped with restriction fragment length polymorphism (RFLP) markers ...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-011-0077-6

    authors: Mohler V,Zeller FJ,Hsam SL

    更新日期:2012-05-01 00:00:00

  • Expression of Npc1 in glial cells corrects sterility in Npc1(-/-) mice.

    abstract::Niemann-Pick type C1 (NPC) disease is an autosomal recessive neurodegenerative disorder. One feature of the mouse model of NPC1 is it's infertility. We have made transgenic mice which express the Npc1 protein exclusively in fibrillary astrocytes, using the glial fibrillary acidic protein (GFAP) promoter. This selectiv...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03195698

    authors: Donohue C,Marion S,Erickson RP

    更新日期:2009-01-01 00:00:00

  • A doubled haploid rye linkage map with a QTL affecting α-amylase activity.

    abstract::A rye doubled haploid (DH) mapping population (Amilo × Voima) segregating for pre-harvest sprouting (PHS) was generated through anther culture of F(1) plants. A linkage map was constructed using DHs, to our knowledge, for the first time in rye. The map was composed of 289 loci: amplified fragment length polymorphism (...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-011-0029-1

    authors: Tenhola-Roininen T,Kalendar R,Schulman AH,Tanhuanpää P

    更新日期:2011-08-01 00:00:00

  • A de novo interstitial 6q deletion in a boy with a split hand malformation.

    abstract::We report on a de novo interstitial deletion of (6)(q15q22.2) in a 5-year-old boy with developmental delay, microcephaly, facial dysmorphism, cryptorchidism, congenital heart defect, and split-hand malformation. Previous reports and this patient suggest that 6q21 may contain a gene or genes related either directly or ...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03195240

    authors: Duran-Gonzalez J,Gutierrez-Angulo M,Garcia-Cruz D,Ayala Mde L,Padilla M,Davalos IP

    更新日期:2007-01-01 00:00:00

  • Development of an efficient retrotransposon-based fingerprinting method for rapid pea variety identification.

    abstract::Fast and efficient DNA fingerprinting of crop cultivars and individuals is frequently used in both theoretical population genetics and in practical breeding. Numerous DNA marker technologies exist and the ratio of speed, cost and accuracy are of importance. Therefore even in species where highly accurate and polymorph...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03194627

    authors: Smýkal P

    更新日期:2006-01-01 00:00:00

  • A new SNP in the promoter region of the porcine MYF5 gene has no effect on its transcript level in m. longissimus dorsi.

    abstract::Myogenic factor 5 (myf-5) is the product of the MYF5 gene, belonging to the MyoD family. This transcription factor participates in the control of myogenesis. We identified 3 new mutations in the promoter region of the gene: A65C, C580T and C613T. The aim of this study was to evaluate the influence of the A65C transver...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03194600

    authors: Urbański P,Flisikowski K,Starzyński RR,Kurył J,Kamyczek M

    更新日期:2006-01-01 00:00:00

  • Genotoxicity of inhalation anaesthetics: DNA lesions generated by sevoflurane in vitro and in vivo.

    abstract::A moderate genotoxic activity of halothane and isoflurane applied as volatile anaesthetics has already been shown. The aim of this work was to estimate a potential genotoxicity of sevoflurane, introduced to clinical practice later than halothane and isoflurane. A genotoxic activity of all three compounds was estimated...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:

    authors: Szyfter K,Szulc R,Mikstacki A,Stachecki I,Rydzanicz M,Jałoszyński P

    更新日期:2004-01-01 00:00:00

  • Relaxed specificity of prokaryotic DNA methyltransferases results in DNA site-specific modification of RNA/DNA heteroduplexes.

    abstract::RNA/DNA hybrid duplexes regularly occur in nature, for example in transcriptional R loops. Their susceptibility to modification by DNA-specific or RNA-specific enzymes is, thus, a biologically relevant question, which, in addition, has possible biotechnological implications. In this study, we investigated the activity...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-015-0279-4

    authors: Wons E,Mruk I,Kaczorowski T

    更新日期:2015-11-01 00:00:00

  • Cardiac ion channel gene mutations in Greek long QT syndrome patients.

    abstract::The long QT syndrome (LQTS) is an inherited cardiac arrhythmia that may lead to sudden death in the absence of structural heart disease. Mutations in the cardiac potassium and sodium channel genes can be found in approximately 70 percent of patients with a highly probable clinical diagnosis. In this study, we aimed to...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03208882

    authors: Kotta CM,Anastasakis A,Gatzoulis K,Papagiannis J,Geleris P,Stefanadis C

    更新日期:2010-01-01 00:00:00

  • Proteolytic enzymes from generative organs of flowering plants (Angiospermae).

    abstract::Pollen proteases were discovered over 100 years ago, whereas the enzymes from female tissues have been used since the Roman era in simple biotechnological processes. In the last decade a great progress has been made in studies on plant proteases, including those from the generative organs. This paper reviews reports p...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章,评审

    doi:

    authors: Radłowski M

    更新日期:2005-01-01 00:00:00

  • Genetic analysis of a red tilapia (Oreochromis spp.) population undergoing three generations of selection for increased body weight at harvest.

    abstract::Quantitative genetic analysis was performed on 10,919 data records collected over three generations from the selection programme for increased body weight at harvest in red tilapia (Oreochromis spp.). They were offspring of 224 sires and 226 dams (50 sires and 60 dams per generation, on average). Linear mixed models w...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-017-0411-8

    authors: Hamzah A,Thoa NP,Nguyen NH

    更新日期:2017-11-01 00:00:00

  • Unique frequencies of HFE gene variants in Roma/Gypsies.

    abstract::The aim of this study was to assess the frequencies of three hemochromatosis gene (HFE) mutations in ethnic Roma/Gypsies in Slovakia. A cohort of 367 individuals representing general population and not preselected for health status was genotyped by TaqMan real-time PCR assay for C282Y, H63D and S65C mutations in HFE g...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-012-0088-y

    authors: Gabriková D,Bernasovská J,Mačeková S,Bôžiková A,Bernasovský I,Bališinová A,Sovičová A,Behulová R,Petrejčíková E,Soták M,Boroňová I

    更新日期:2012-05-01 00:00:00

  • Founder event and its effect on genetic variation in translocated populations of noble crayfish (Astacus astacus).

    abstract::Establishing translocated populations is a common process to preserve and maintain genetic diversity of threatened species. In 2001, three translocated populations of noble crayfish (Astacus astacus) were established in the Czech Republic, founded by either adult or juvenile individuals from three particular source po...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-015-0296-3

    authors: Bláha M,Žurovcová M,Kouba A,Policar T,Kozák P

    更新日期:2016-02-01 00:00:00

  • Expression analysis of somatic embryogenesis-related SERK, LEC1, VP1 and NiR ortologues in rye (Secale cereale L.).

    abstract::The genetic basis of the regeneration process in cultured immature embryos of rye (Secale cereale L.) was analyzed. The experiments were designed to reveal differences between the in vitro culture responses of two inbred lines: L318 (a high regeneration ability) and L9 (a low potential for regeneration). The rye ortol...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-010-0015-z

    authors: Gruszczyńska A,Rakoczy-Trojanowska M

    更新日期:2011-02-01 00:00:00

  • Epigenetic chromatin modifications in barley after mutagenic treatment.

    abstract::In addition to their normal developmental processes, plants have evolved complex genetic and epigenetic regulatory mechanisms to cope with various environmental stresses. It has been shown that both DNA methylation and histone modifications are involved in DNA damage response to various types of stresses. In this stud...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-014-0226-9

    authors: Braszewska-Zalewska A,Tylikowska M,Kwasniewska J,Szymanowska-Pulka J

    更新日期:2014-11-01 00:00:00

  • New PAH gene promoter KLF1 and 3'-region C/EBPalpha motifs influence transcription in vitro.

    abstract::Phenylketonuria (PKU) is a metabolic disease caused by mutations in the phenylalanine hydroxylase (PAH) gene. Although the PAH genotype remains the main determinant of PKU phenotype severity, genotype-phenotype inconsistencies have been reported. In this study, we focused on unanalysed sequences in non-coding PAH gene...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-016-0359-0

    authors: Klaassen K,Stankovic B,Kotur N,Djordjevic M,Zukic B,Nikcevic G,Ugrin M,Spasovski V,Srzentic S,Pavlovic S,Stojiljkovic M

    更新日期:2017-02-01 00:00:00

  • Genetic control of bacterial biofilms.

    abstract::Nearly all bacterial species, including pathogens, have the ability to form biofilms. Biofilms are defined as structured ecosystems in which microbes are attached to surfaces and embedded in a matrix composed of polysaccharides, eDNA, and proteins, and their development is a multistep process. Bacterial biofilms const...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章,评审

    doi:10.1007/s13353-015-0309-2

    authors: Wolska KI,Grudniak AM,Rudnicka Z,Markowska K

    更新日期:2016-05-01 00:00:00

  • QTL mapping of 1000-kernel weight, kernel length, and kernel width in bread wheat (Triticum aestivum L.).

    abstract::Kernel size and morphology influence the market value and milling yield of bread wheat (Triticum aestivum L.). The objective of this study was to identify quantitative trait loci (QTLs) controlling kernel traits in hexaploid wheat. We recorded 1000-kernel weight, kernel length, and kernel width for 185 recombinant inb...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03208872

    authors: Ramya P,Chaubal A,Kulkarni K,Gupta L,Kadoo N,Dhaliwal HS,Chhuneja P,Lagu M,Gupta V

    更新日期:2010-01-01 00:00:00

  • First results on the genetic diversity of the invasive signal crayfish Pacifastacus leniusculus (Dana, 1852) in Europe using novel microsatellite loci.

    abstract::The introduction of non-native crayfish in aquatic ecosystems is very common due to human activities (e.g. aquaculture, recreational and commercial fisheries). The signal crayfish, Pacifastacus leniusculus (Dana, 1852), is one of the most widespread invasive species in Europe. Although several important ecological and...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-015-0272-y

    authors: Froufe E,Varandas S,Teixeira A,Sousa R,Filipová L,Petrusek A,Edsman L,Lopes-Lima M

    更新日期:2015-08-01 00:00:00

  • Inheritance of seed dormancy in Tibetan semi-wild wheat accession Q1028.

    abstract::Tibetan semi-wild wheat (Triticum aestivum ssp. tibetanum Shao) is one of the Chinese endemic hexaploid wheat genetic resources, distributed only in the Qinghai-Xizang Plateau of China. It has special characters, such as a hulled glume and spike disarticulation. However, seed dormancy, another important character for ...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:

    authors: Lan XJ,Wei YM,Liu DC,Yan ZH,Zheng YL

    更新日期:2005-01-01 00:00:00

  • Fingerprinting of common wheat cultivars with an Alw44I-based AFLP method.

    abstract::A simplified AFLP method, based on methylation-sensitive Alw44I restriction endonuclease, has been developed and evaluated for fingerprinting 15 wheat cultivars. The selected germplasms represented groups of spring and winter wheats with and without the 1BL.1RS translocation. Ten selective primers yielded 57 markers, ...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:

    authors: Tyrka M

    更新日期:2004-01-01 00:00:00

  • QTL analysis of falling number and seed longevity in wheat (Triticum aestivum L.).

    abstract::Pre-harvest sprouting (PHS) and seed longevity (SL) are complex biological processes of major importance for agricultural production. In the present study, a recombinant inbred line (RIL) population derived from a cross between the German winter wheat (Triticum aestivum L.) cultivars History and Rubens was used to ide...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-017-0422-5

    authors: Börner A,Nagel M,Agacka-Mołdoch M,Gierke PU,Oberforster M,Albrecht T,Mohler V

    更新日期:2018-02-01 00:00:00

  • Sequence characteristics and divergent evolution of the chloroplast psbA-trnH noncoding region in gymnosperms.

    abstract::The psbA-trnH intergenic region is among the most variable regions in the gymnosperm chloroplast genome. It is proposed as suitable for DNA barcoding studies and is useful in phylogenetics at the species level. This region consists of two parts differing in their evolutionary characteristics: 1) the psbA 3’UTR (...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03208855

    authors: Hao DC,Chen SL,Xiao PG

    更新日期:2010-01-01 00:00:00

  • Cytogenetic investigation of Arctic char × brook trout F1, F2 and backcross hybrids revealed remnants of the chromosomal rearrangements.

    abstract::Arctic char (Salvelinus alpinus) and brook trout (Salvelinus fontinalis) hybridize and their offspring is viable and fertile. This may be a real treat for the native European stocks of Arctic char which gene pools might be unintendedly contaminated with the genetic elements of brook trout. On the other hand, hybrids o...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-020-00584-2

    authors: Pomianowski K,Ocalewicz K

    更新日期:2021-02-01 00:00:00