Search Results - "Tomiuk, J."
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Avian Clock gene polymorphism: evidence for a latitudinal cline in allele frequencies
Published in Molecular ecology (01-11-2007)“…In comparison with most animal behaviours, circadian rhythms have a well-characterized molecular genetic basis. Detailed studies of circadian clock genes in…”
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Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease
Published in Human molecular genetics (15-04-2008)“…A polyglutamine repeat expansion of more than 36 units in a protein called huntingtin (htt) is the only known cause of Huntington's disease (HD). The expanded…”
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The genetic dynamics of the rapid and recent colonization of Denmark by Arion lusitanicus (Mollusca, Pulmonata, Arionidae)
Published in Genetica (01-06-2011)“…We describe the genetic dynamics of the recent establishment of the ‘Iberian slug’, Arion lusitanicus J. Mabille 1868, in Denmark and compare its population…”
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Prospective comparison of PCR-based vs late mRNA-based preemptive antiviral therapy for HCMV infection in patients after allo-SCT
Published in Bone marrow transplantation (Basingstoke) (01-03-2011)“…Human CMV (HCMV)-directed preemptive therapy has helped to improve the outcome following allo-SCT. In this study, we evaluated the safety and efficacy of a…”
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High Rates of Extra-Pair Young in the Pair-Living Fat-Tailed Dwarf Lemur, Cheirogaleus medius
Published in Behavioral ecology and sociobiology (04-12-2000)“…Cheirogaleids are one of the most primitive extant primate taxa in the world. Their lifestyle and mating system, therefore, have been considered to be…”
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Maintenance of clonal diversity in Dipsa bifurcata (Fallen, 1810) (Diptera: Lonchopteridae). I. Fluctuating seasonal selection moulds long-term coexistence
Published in Heredity (01-07-2004)“…The deterministic maintenance of clonal diversity in thelytokous taxa can be seen as a model for understanding how environmental heterogeneity both can…”
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POPDIST, version 1.1.1: a program to calculate population genetic distance and identity measures
Published in The Journal of heredity (01-03-2000)Get full text
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Maintenance of clonal diversity in Dipsa bifurcata (Fallén, 1810) (Diptera: Lonchopteridae). II. Diapause stabilizes clonal coexistence
Published in Heredity (01-07-2004)“…We analyze a selection model analogous to a one-locus, two-allele haploid system that can explain recurrent seasonal changes in diversity for communities with…”
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A- or C-chromosomes, does it matter for the transfer of transgenes from Brassica napus
Published in Theoretical and applied genetics (01-03-2000)“…Introgression of genes from allotetraploid Brassica napus into its diploid wild relative B. rapa is generally considered to be inevitable. As a means to…”
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Population differentiation through mutation and drift--a comparison of genetic identity measures
Published in Genetica (01-01-1998)“…Different genetic identity or distance measures are compared that consider allelic variation within and between populations. Particularily we analyse those…”
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Genetic variations of the SLC7A9 gene: allele distribution of 13 polymorphic sites in German cystinuria patients and controls
Published in Clinical nephrology (01-05-2003)“…Cystinuria is a hereditary disorder of cystine and dibasic amino acid transport across the luminal membrane of renal tubules and intestine, resulting in…”
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Simultaneous analysis of interleukin-10 gene microsatellites and single-nucleotide polymorphisms in parallel with tumour necrosis factor and interferon-gamma short tandem repeats by fluorescence-based polymerase chain reaction
Published in Genes and immunity (01-10-2003)“…Different cytokine genotypes exist in the population, for example, as a result of selective pressure of infectious diseases. It may be that specific cytokine…”
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Analysis of the genes SLC7A9 and SLC3A1 in unclassified cystinurics: mutation detection rates and association between variants in SLC7A9 and the disease
Published in Clinical nephrology (01-05-2002)“…Cystinuria is a common inherited disorder of defective renal reabsorption of cystine and dibasic amino acids. Recently, 2 responsible genes have been…”
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Temporal and spatial analyses disclose consequences of habitat fragmentation on the genetic diversity in capercaillie (Tetrao urogallus)
Published in Molecular ecology (01-05-2008)“…As a result of habitat fragmentation, the capercaillie (Tetrao urogallus) population in the Black Forest mountain range in southwestern Germany has declined…”
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A new measure of genetic identity between populations of sexual and asexual species
Published in Evolution (01-11-1991)“…We define a new genetic identity measure that is especially well suited for asexual polyploid species as it circumvents errors in the estimation of gene…”
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Semiautomated and simultaneous analysis of the interleukin-10 gene microsatellites IL-10G and IL-10R by fluorescence-based polymerase chain reaction reveals significant differences in allele distributions between Caucasians (Germany) and Africans (Gabon)
Published in European cytokine network (Montrouge) (01-07-2001)“…Interleukin-10 (IL-10) is an important immunoregulatory cytokine influencing many aspects of the adaptive and inflammatory immune response. Two dinucleotide…”
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Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders
Published in International journal of molecular medicine (01-07-2001)“…Traditional linkage analysis in large families is the most promising approach for mapping disease genes of monogenic heritable disorders when the number of…”
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On the Application of Birth-Death Models in Conservation Biology
Published in Conservation biology (01-06-1994)“…The aim of this paper first is to discuss the application of the commonly used equations for the mean expected extinction time of a population as presented by…”
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Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneity
Published in International journal of molecular medicine (01-02-2001)“…A number of distinct, partly non-overlapping genetic loci have been reported for the complete type of X-linked congenital stationary night blindness (CSNB1),…”
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