Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Publikationen
Suchbegriffe: BASE SEQUENCE - , . Treffer: 299
2018
Matzhold, EM; Drexler, C; Staudacher, E; Glock, B; Wagner, T
A novel variant B allele at the ABO gene locus characterized by a duplication-based insertion of 27 nucleotides identified in an Iraqi male with a weak B subgroup phenotype.
Transfusion. 2018; 58(5):1318-1319
Doi: 10.1111/trf.14539
(- Case Report)
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
2017
Jahic, A; Hinreiner, S; Emberger, W; Hehr, U; Zuchner, S; Beetz, C
Doublet-Mediated DNA Rearrangement-A Novel and Potentially Underestimated Mechanism for the Formation of Recurrent Pathogenic Deletions.
Hum Mutat. 2017; 38(3):275-278
Doi: 10.1002/humu.23162
Web of Science
PubMed
FullText
FullText_MUG
Kintz, E; Heiss, C; Black, I; Donohue, N; Brown, N; Davies, MR; Azadi, P; Baker, S; Kaye, PM; van der Woude, M
Salmonella enterica Serovar Typhi Lipopolysaccharide O-Antigen Modification Impact on Serum Resistance and Antibody Recognition.
Infect Immun. 2017; 85(4):
Doi: 10.1128/IAI.01021-16
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Ofner, R; Ritter, C; Ugurel, S; Cerroni, L; Stiller, M; Bogenrieder, T; Solca, F; Schrama, D; Becker, JC
Non-reproducible sequence artifacts in FFPE tissue: an experience report.
J Cancer Res Clin Oncol. 2017; 143(7):1199-1207
Doi: 10.1007/s00432-017-2399-1
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
2016
Hartmann, L; Dutta, S; Opatz, S; Vosberg, S; Reiter, K; Leubolt, G; Metzeler, KH; Herold, T; Bamopoulos, SA; Bräundl, K; Zellmeier, E; Ksienzyk, B; Konstandin, NP; Schneider, S; Hopfner, KP; Graf, A; Krebs, S; Blum, H; Middeke, JM; Stölzel, F; Thiede, C; Wolf, S; Bohlander, SK; Preiss, C; Chen-Wichmann, L; Wichmann, C; Sauerland, MC; Büchner, T; Berdel, WE; Wörmann, BJ; Braess, J; Hiddemann, W; Spiekermann, K; Greif, PA
ZBTB7A mutations in acute myeloid leukaemia with t(8;21) translocation.
Nat Commun. 2016; 7(1): 11733-11733.
Doi: 10.1038/ncomms11733
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Polin, H; Pelc-Klopotowska, M; Danzer, M; Suessner, S; Gabriel, C; Wilflingseder, J; Żmudzin, A; Orzińska, A; Guz, K; Michalewska, B; Brojer, E
Compound heterozygosity of two novel RHAG alleles leads to a considerable disruption of the Rh complex.
Transfusion. 2016; 56(4):950-955
Doi: 10.1111/trf.13476
(- Case Report)
Web of Science
PubMed
FullText
FullText_MUG
Ulrich, S; Posch, U; Helmberg, W; Schlenke, P
HLA-A*68:02:11, a new HLA-A*68 allele identified during family HLA typing.
HLA. 2016; 88(4):197-198
Doi: 10.1111/tan.12875
Web of Science
PubMed
FullText
FullText_MUG
2015
Boch, T; Reinwald, M; Postina, P; Cornely, OA; Vehreschild, JJ; Heußel, CP; Heinz, WJ; Hoenigl, M; Eigl, S; Lehrnbecher, T; Hahn, J; Claus, B; Lauten, M; Egerer, G; Müller, MC; Will, S; Merker, N; Hofmann, WK; Buchheidt, D; Spiess, B
Identification of invasive fungal diseases in immunocompromised patients by combining an Aspergillus specific PCR with a multifungal DNA-microarray from primary clinical samples.
Mycoses. 2015; 58(12):735-745
Doi: 10.1111/myc.12424
Web of Science
PubMed
FullText
FullText_MUG
Chromikova, V; Mader, A; Hofbauer, S; Göbl, C; Madl, T; Gach, JS; Bauernfried, S; Furtmüller, PG; Forthal, DN; Mach, L; Obinger, C; Kunert, R
Introduction of germline residues improves the stability of anti-HIV mAb 2G12-IgM.
Biochim Biophys Acta. 2015; 1854(10 Pt A):1536-1544
Doi: 10.1016/j.bbapap.2015.02.018
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Kassner, U; Salewsky, B; Wühle-Demuth, M; Szijarto, IA; Grenkowitz, T; Binner, P; März, W; Steinhagen-Thiessen, E; Demuth, I
Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants.
Eur J Hum Genet. 2015; 23(9):1259-1261
Doi: 10.1038/ejhg.2014.295
(- Case Report)
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Rafiq, MA; Leblond, CS; Saqib, MA; Vincent, AK; Ambalavanan, A; Khan, FS; Ayaz, M; Shaheen, N; Spiegelman, D; Ali, G; Amin-ud-Din, M; Laurent, S; Mahmood, H; Christian, M; Ali, N; Fennell, A; Nanjiani, Z; Egger, G; Caron, C; Waqas, A; Ayub, M; Rasheed, S; Forgeot d'Arc, B; Johnson, A; So, J; Brohi, MQ; Mottron, L; Ansar, M; Vincent, JB; Xiong, L
Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features.
BMC Med Genet. 2015; 16(7):41-41
Doi: 10.1186/s12881-015-0183-0
(- Case Report)
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Wagner, B; Melzer, H; Freymüller, G; Stumvoll, S; Rendi-Wagner, P; Paulke-Korinek, M; Repa, A; Mooi, FR; Kollaritsch, H; Mittermayer, H; Kessler, HH; Stanek, G; Steinborn, R; Duchêne, M; Wiedermann, U
Genetic Variation of Bordetella pertussis in Austria.
PLoS One. 2015; 10(7):e0132623-e0132623
Doi: 10.1371/journal.pone.0132623
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Zopf, A; Raim, R; Danzer, M; Niklas, N; Spilka, R; Pröll, J; Gabriel, C; Nechansky, A; Roucka, M
Introduction of the hybcell-based compact sequencing technology and comparison to state-of-the-art methodologies for KRAS mutation detection.
Biotechniques. 2015; 58(3):126-134
Doi: 10.2144/000114264
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
2014
Akilzhanova, A; Guelly, C; Nuralinov, O; Nurkina, Z; Nazhat, D; Smagulov, S; Tursunbekov, A; Alzhanova, A; Rashbayeva, G; Abdrakhmanov, A; Dosmagambet, S; Trajanoski, S; Zhumadilov, Z; Sharman, A; Bekbosynova, M
RYR2 sequencing reveals novel missense mutations in a Kazakh idiopathic ventricular tachycardia study cohort.
PLoS One. 2014; 9(6):e101059-e101059
Doi: 10.1371/journal.pone.0101059
(- Case Report)
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Bernkopf, M; Webersinke, G; Tongsook, C; Koyani, CN; Rafiq, MA; Ayaz, M; Müller, D; Enzinger, C; Aslam, M; Naeem, F; Schmidt, K; Gruber, K; Speicher, MR; Malle, E; Macheroux, P; Ayub, M; Vincent, JB; Windpassinger, C; Duba, HC
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability.
Hum Mol Genet. 2014; 23(15):4015-4023
Doi: 10.1093/hmg/ddu115
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Goessweiner-Mohr, N; Eder, M; Hofer, G; Fercher, C; Arends, K; Birner-Gruenberger, R; Grohmann, E; Keller, W
Structure of the double-stranded DNA-binding type IV secretion protein TraN from Enterococcus.
Acta Crystallogr D Biol Crystallogr. 2014; 70(Pt 9):2376-2389
Doi: 10.1107/S1399004714014187
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Heidenreich, B; Nagore, E; Rachakonda, PS; Garcia-Casado, Z; Requena, C; Traves, V; Becker, J; Soufir, N; Hemminki, K; Kumar, R
Telomerase reverse transcriptase promoter mutations in primary cutaneous melanoma.
Nat Commun. 2014; 5(5):3401-3401
Doi: 10.1038/ncomms4401
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Hetz, S; Acikgoez, A; Voss, U; Nieber, K; Holland, H; Hegewald, C; Till, H; Metzger, R; Metzger, M
In vivo transplantation of neurosphere-like bodies derived from the human postnatal and adult enteric nervous system: a pilot study.
PLoS One. 2014; 9(4):e93605-e93605
Doi: 10.1371/journal.pone.0093605
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Kastner, R; Zopf, A; Preuner, S; Pröll, J; Niklas, N; Foskett, P; Valent, P; Lion, T; Gabriel, C
Rapid identification of compound mutations in patients with Philadelphia-positive leukaemias by long-range next generation sequencing.
Eur J Cancer. 2014; 50(4): 793-800.
Doi: 10.1016/j.ejca.2013.11.030
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Khan, MA; Rupp, V; Khan, MA; Khan, MP; Ansar, M; Windpassinger, C
Genetic analysis of a consanguineous Pakistani family with Leber congenital amaurosis identifies a novel mutation in GUCY2D gene.
J Genet. 2014; 93(2):527-530
Doi: 10.1007/s12041-014-0394-8
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Khan, MA; Rupp, VM; Orpinell, M; Hussain, MS; Altmüller, J; Steinmetz, MO; Enzinger, C; Thiele, H; Höhne, W; Nürnberg, G; Baig, SM; Ansar, M; Nürnberg, P; Vincent, JB; Speicher, MR; Gönczy, P; Windpassinger, C
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family.
Hum Mol Genet. 2014; 23(22):5940-5949
Doi: 10.1093/hmg/ddu318
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Kienesberger, S; Sprenger, H; Wolfgruber, S; Halwachs, B; Thallinger, GG; Perez-Perez, GI; Blaser, MJ; Zechner, EL; Gorkiewicz, G
Comparative genome analysis of Campylobacter fetus subspecies revealed horizontally acquired genetic elements important for virulence and niche specificity.
PLoS One. 2014; 9(1):e85491-e85491
Doi: 10.1371/journal.pone.0085491
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Lee, W; Teckie, S; Wiesner, T; Ran, L; Prieto Granada, CN; Lin, M; Zhu, S; Cao, Z; Liang, Y; Sboner, A; Tap, WD; Fletcher, JA; Huberman, KH; Qin, LX; Viale, A; Singer, S; Zheng, D; Berger, MF; Chen, Y; Antonescu, CR; Chi, P
PRC2 is recurrently inactivated through EED or SUZ12 loss in malignant peripheral nerve sheath tumors.
Nat Genet. 2014; 46(11): 1227-1232.
Doi: 10.1038/ng.3095
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Liu, L; Huang, C; He, ZG
A TetR family transcriptional factor directly regulates the expression of a 3-methyladenine DNA glycosylase and physically interacts with the enzyme to stimulate its base excision activity in Mycobacterium bovis BCG.
J Biol Chem. 2014; 289(13):9065-9075
Doi: 10.1074/jbc.M113.528919
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Niklas, N; Pröll, J; Weinberger, J; Zopf, A; Wiesinger, K; Krismer, K; Bettelheim, P; Gabriel, C
Qualifying high-throughput immune repertoire sequencing.
Cell Immunol. 2014; 288(1-2): 31-38.
Doi: 10.1016/j.cellimm.2014.02.001
Web of Science
PubMed
FullText
FullText_MUG
Oh, DY; Walenta, E; Akiyama, TE; Lagakos, WS; Lackey, D; Pessentheiner, AR; Sasik, R; Hah, N; Chi, TJ; Cox, JM; Powels, MA; Di Salvo, J; Sinz, C; Watkins, SM; Armando, AM; Chung, H; Evans, RM; Quehenberger, O; McNelis, J; Bogner-Strauss, JG; Olefsky, JM
A Gpr120-selective agonist improves insulin resistance and chronic inflammation in obese mice.
Nat Med. 2014; 20(8): 942-947.
Doi: 10.1038/nm.3614
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Polin, H; Danzer, M; Reiter, A; Brisner, M; Gaszner, W; Weinberger, J; Gabriel, C
MN typing discrepancies based on GYPA-B-A hybrid.
Vox Sang. 2014; 107(4): 393-398.
Doi: 10.1111/vox.12168
Web of Science
PubMed
FullText
FullText_MUG
Shah, MH; Bhat, V; Shetty, JS; Kumar, A
Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome.
Mol Vis. 2014; 20(4):790-796
(- Case Report)
[OPEN ACCESS]
Web of Science
PubMed
Wiesner, T; He, J; Yelensky, R; Esteve-Puig, R; Botton, T; Yeh, I; Lipson, D; Otto, G; Brennan, K; Murali, R; Garrido, M; Miller, VA; Ross, JS; Berger, MF; Sparatta, A; Palmedo, G; Cerroni, L; Busam, KJ; Kutzner, H; Cronin, MT; Stephens, PJ; Bastian, BC
Kinase fusions are frequent in Spitz tumours and spitzoid melanomas.
Nat Commun. 2014; 5(5):3116-3116
Doi: 10.1038/ncomms4116
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
2013
Bauer, R; Plieschnig, JA; Finkes, T; Riegler, B; Hermann, M; Schneider, WJ
The developing chicken yolk sac acquires nutrient transport competence by an orchestrated differentiation process of its endodermal epithelial cells.
J Biol Chem. 2013; 288(2): 1088-1098.
Doi: 10.1074/jbc.M112.393090
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Duszka, K; Bogner-Strauss, JG; Hackl, H; Rieder, D; Neuhold, C; Prokesch, A; Trajanoski, Z; Krogsdam, AM
Nr4a1 is required for fasting-induced down-regulation of Pparγ2 in white adipose tissue.
Mol Endocrinol. 2013; 27(1): 135-149.
Doi: 10.1210/me.2012-1248
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Eggermann, T; Spengler, S; Denecke, B; Zerres, K; Mache, CJ
Multi-exon deletion in the XDH gene as a cause of classical xanthinuria.
Clin Nephrol. 2013; 79(1):78-80
Doi: 10.5414/CN106994
(- Case Report)
Web of Science
PubMed
FullText
FullText_MUG
Eißmann, M; Melzer, IM; Fernández, SB; Michel, G; Hrabě de Angelis, M; Hoefler, G; Finkenwirth, P; Jauch, A; Schoell, B; Grez, M; Schmidt, M; Bartholomae, CC; Newrzela, S; Haetscher, N; Rieger, MA; Zachskorn, C; Mittelbronn, M; Zörnig, M
Overexpression of the anti-apoptotic protein AVEN contributes to increased malignancy in hematopoietic neoplasms.
Oncogene. 2013; 32(20):2586-2591
Doi: 10.1038/onc.2012.263
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Fischer, C; Koblmüller, S; Gülly, C; Schlötterer, C; Sturmbauer, C; Thallinger, GG
Complete mitochondrial DNA sequences of the threadfin cichlid (Petrochromis trewavasae) and the blunthead cichlid (Tropheus moorii) and patterns of mitochondrial genome evolution in cichlid fishes.
PLoS One. 2013; 8(6):e67048-e67048
Doi: 10.1371/journal.pone.0067048
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Gottschalk, B; Klein, A
Restoration of wild-type p53 in drug-resistant mouse breast cancer cells leads to differential gene expression, but is not sufficient to overcome the malignant phenotype.
Mol Cell Biochem. 2013; 379(1-2): 213-227.
Doi: 10.1007/s11010-013-1643-5
Web of Science
PubMed
FullText
FullText_MUG
Ivashov, VA; Grillitsch, K; Koefeler, H; Leitner, E; Baeumlisberger, D; Karas, M; Daum, G
Lipidome and proteome of lipid droplets from the methylotrophic yeast Pichia pastoris.
Biochim Biophys Acta. 2013; 1831(2):282-290
Doi: 10.1016/j.bbalip.2012.09.017
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Lionel, AC; Vaags, AK; Sato, D; Gazzellone, MJ; Mitchell, EB; Chen, HY; Costain, G; Walker, S; Egger, G; Thiruvahindrapuram, B; Merico, D; Prasad, A; Anagnostou, E; Fombonne, E; Zwaigenbaum, L; Roberts, W; Szatmari, P; Fernandez, BA; Georgieva, L; Brzustowicz, LM; Roetzer, K; Kaschnitz, W; Vincent, JB; Windpassinger, C; Marshall, CR; Trifiletti, RR; Kirmani, S; Kirov, G; Petek, E; Hodge, JC; Bassett, AS; Scherer, SW
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.
Hum Mol Genet. 2013; 22(10):2055-2066
Doi: 10.1093/hmg/ddt056
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Merkel, OM; Marsh, LM; Garn, H; Kissel, T
Flow cytometry-based cell type-specific assessment of target regulation by pulmonary siRNA delivery.
Methods Mol Biol. 2013; 948(3):263-273
Doi: 10.1007/978-1-62703-140-0_18
[OPEN ACCESS]
PubMed
FullText
FullText_MUG
Nevado, B; Mautner, S; Sturmbauer, C; Verheyen, E
Water-level fluctuations and metapopulation dynamics as drivers of genetic diversity in populations of three Tanganyikan cichlid fish species.
Mol Ecol. 2013; 22(15): 3933-3948.
Doi: 10.1111/mec.12374
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Novakovic, B; Gordon, L; Robinson, WP; Desoye, G; Saffery, R
Glucose as a fetal nutrient: dynamic regulation of several glucose transporter genes by DNA methylation in the human placenta across gestation.
J Nutr Biochem. 2013; 24(1):282-288
Doi: 10.1016/j.jnutbio.2012.06.006
Web of Science
PubMed
FullText
FullText_MUG
Opatz, S; Polzer, H; Herold, T; Konstandin, NP; Ksienzyk, B; Zellmeier, E; Vosberg, S; Graf, A; Krebs, S; Blum, H; Hopfner, KP; Kakadia, PM; Schneider, S; Dufour, A; Braess, J; Sauerland, MC; Berdel, WE; Büchner, T; Woermann, BJ; Hiddemann, W; Spiekermann, K; Bohlander, SK; Greif, PA
Exome sequencing identifies recurring FLT3 N676K mutations in core-binding factor leukemia.
Blood. 2013; 122(10): 1761-1769.
Doi: 10.1182/blood-2013-01-476473
Web of Science
PubMed
FullText
FullText_MUG
Probst, AJ; Auerbach, AK; Moissl-Eichinger, C
Archaea on human skin.
PLoS One. 2013; 8(6):e65388-e65388
Doi: 10.1371/journal.pone.0065388
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Schwendner, P; Moissl-Eichinger, C; Barczyk, S; Bohmeier, M; Pukall, R; Rettberg, P
Insights into the microbial diversity and bioburden in a South American spacecraft assembly clean room.
Astrobiology. 2013; 13(12):1140-1154
Doi: 10.1089/ast.2013.1023
Web of Science
PubMed
FullText
FullText_MUG
Ulrich, S; Posch, U; Lanzer, G
Detection of a new HLA-A allele, designated HLA-A*32:53.
Tissue Antigens. 2013; 82(5):348-348
Doi: 10.1111/tan.12205
Web of Science
PubMed
FullText
FullText_MUG
2012
Crnkovic, S; Riederer, M; Lechleitner, M; Hallström, S; Malli, R; Graier, WF; Lindenmann, J; Popper, H; Olschewski, H; Olschewski, A; Frank, S
Docosahexaenoic acid-induced unfolded protein response, cell cycle arrest, and apoptosis in vascular smooth muscle cells are triggered by Ca²⁺-dependent induction of oxidative stress.
Free Radic Biol Med. 2012; 52(9):1786-1795
Doi: 10.1016/j.freeradbiomed.2012.02.036
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Hafner, C; Houben, R; Baeurle, A; Ritter, C; Schrama, D; Landthaler, M; Becker, JC
Activation of the PI3K/AKT pathway in Merkel cell carcinoma.
PLoS One. 2012; 7(2):e31255-e31255
Doi: 10.1371/journal.pone.0031255
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Huppke, P; Brendel, C; Kalscheuer, V; Korenke, GC; Marquardt, I; Freisinger, P; Christodoulou, J; Hillebrand, M; Pitelet, G; Wilson, C; Gruber-Sedlmayr, U; Ullmann, R; Haas, S; Elpeleg, O; Nürnberg, G; Nürnberg, P; Dad, S; Mller, LB; Kaler, SG; Gärtner, J
Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.
AM J HUM GENET. 2012; 90(1): 61-68.
Doi: 10.1016/j.ajhg.2011.11.030
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Lajin, B; Alachkar, A; Alhaj Sakur, A
A quadruplex tetra-primer ARMS-PCR method for the simultaneous detection of TP53 Arg72Pro, IVS3 16bp Del/Ins and IVS6+62A>G, and NQO1 C609T polymorphisms.
Gene. 2012; 504(2):268-273
Doi: 10.1016/j.gene.2012.05.024
Web of Science
PubMed
FullText
FullText_MUG
Liu, SJ; Tetzlaff, MT; Liu, AH; Liegl-Atzwanger, B; Guo, J; Xu, XW;
Loss of microRNA-205 expression is associated with melanoma progression.
Lab Invest. 2012; 92(7):1084-1096
Doi: 10.1038/labinvest.2012.62
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Simon, UK; Trajanoski, S; Kroneis, T; Sedlmayr, P; Guelly, C; Guttenberger, H
Accession-specific haplotypes of the internal transcribed spacer region in Arabidopsis thaliana--a means for barcoding populations.
Mol Biol Evol. 2012; 29(9):2231-2239
Doi: 10.1093/molbev/mss093
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Weitere 50 Treffer anzeigen