Mouse chromosome 17
Screening of genetic loci predisposing to herpes simplex virus infection on mouse chromosome 17
... inbred mouse lines with significantly distinct predisposition to HSV infection were chosen for gene loci ...on mouse chromosome 17 associated with susceptibility to HSV infection were then ...
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SEVERAL GALACTOSYLTRANSFERASE ACTIVITIES ARE ASSOCIATED WITH MOUSE CHROMOSOME 17
... Because the galactosyltransferase assays were performed with UDP-Gal con- centrations that are very close to the typical K,,, values for these enzymes in other system[r] ...
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ETHYLNITROSOUREA MUTAGENESIS AND THE ISOLATION OF MUTANT ALLELES FOR SPECIFIC GENES LOCATED IN THE t REGION OF MOUSE CHROMOSOME 17
... One mutagen- ized male gave two quaking progeny (qk' and qkk2). Table 5 presents data from these males demonstrating the heritability, recessive phenotype and probable l[r] ...
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ARYL HYDROCARBON HYDROXYLASE INDUCTION BY BENZO[a]ANTHRACENE: REGULATORY GENE LOCALIZED TO THE DISTAL PORTION OF MOUSE CHROMOSOME 17
... Aryl hydrocarbon (benzo[a]pyrene) hydroxylase inducibility by benzo[a]an- thracene was studied in 29 somatic cell hybrid clones, developed by fusing mouse spleen or per[r] ...
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The proximal end of mouse chromosome 17: new molecular markers identify a deletion associated with quakingviable.
... In situ hybridization of 6.5 to 18.5 days post coitum embryos shows that message is present in all stages, but becomes confined mainly to the developing central nervo[r] ...
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THE LOCUS ENCODING αA-CRYSTALLIN IS CLOSELY LINKED TO H-2K ON MOUSE CHROMOSOME 17
... To facili- tate studies of the genetics of lens crystallins and their involvement in heritable lens defects in mice, we have identified DNA restriction fragment length pol-[r] ...
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A novel mouse chromosome 17 hybrid sterility locus: implications for the origin of t haplotypes.
... M. spretus-origin model of t haplotypes is that these chromosomes might not distort transmission ratios as drastically in a heterozygous combination with the M. spretus form [r] ...
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Narrowing the Critical Regions for Mouse t Complex Transmission Ratio Distortion Factors by Use of Deletions
... Previously a deletion in mouse chromosome 17, T 22H , was shown to behave like a t allele of the t complex distorter gene Tcd1, and this was attributed to deletion of this locus.. Seven [r] ...
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CHARACTERIZATION OF A RECOMBINANT MOUSE t HAPLOTYPE THAT EXPRESSES A DOMINANT LETHAL MATERNAL EFFECT
... We report here the discovery of another mutant form of mouse chromosome 17 that expresses a maternal effect very similar to that associated with the ThP deletion.. This novel[r] ...
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Molecular Cloning, Chromosomal Mapping, and Characterization of the Human Cardiac-Specific Homeobox Gene hCsx
... Synteny homology of mouse chromosome 17, where the Csx/Nkx2.5 gene maps, suggested that the human homolog would likely reside on chro- mosome 6 (Fig. The localization of hCsx to the dist[r] ...
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Cystic Dilation of the Aqueductus Sylvii in Case of Trisomy 17p11.2—pter with the Deletion of the Terminal Portion of the Chromosome 6
... study involved chromosome 17. One of these cases, the nuchal translucency thickness was 3.1 mm, but in the other it was only 1.3 mm [15]. There is no doubt that first trimester ultrasound examination has a ...
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Pgk1 and Hprt gene activity in the peri implantation mouse embryo is influenced by the parental origin of the X chromosome
... Further validation of the allele-specificity of the SNuPE assay was performed on XY blastocysts which only express the X-linked allele from the maternally derived X-chromosome. Four XY blastocysts each from mice ...
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Non-coding RNAs enter mitosis: functions, conservation and implications
... and mouse Piwi homologues, Hiwi, PiwiL2, and PiwiL2-like proteins, are expressed in certain human and mouse stem cells and tumors [54-57], raising the possibility that the development of cancer may be ...
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The pseudoautosomal region of the mouse
... and SYN1 on the human and mouse X chromosome and the evolutionary breakpoint on the eutherian X chromosome could be refined to being located between U B E I and MAOA... As several[r] ...
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More biology from the sequence
... the mouse and rat would appear to be significant out- liers from the general trend being substantially more divergent than ...the mouse genome and its use in the comparative annotation of other ...shotgun ...
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The PEG13 -DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus
... The mouse chromosome 15 imprinted cluster contains multiple brain-specific maternally expressed transcripts including Ago2, Chrac1, Trappc9 and Kcnk9 and a paternally expressed gene, ...on chromosome ...
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6252.pdf
... Figure 3-2. Bisulfite sequencing analysis of the Actn1 DMR in mouse, rat and human tissues. Panel A shows bisulfite sequencing results from clones isolated from rat liver, mouse liver, and human ...
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Genetics and physical mapping studies on mouse chromosome 2
... The mouse/hamster hybrid cell line EBS-18/AZ was derived from line EBS-18 (Lalley et ...X chromosome using minimal essential medium supplemented with azaguanine as described (Abbott and Povey, ...
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Bipartite structure of the inactive mouse X chromosome
... We found that regions enriched in CTCF binding on the Xi tended to be located at the periphery of the 3D structure, suggesting that these loci may serve as attach- ment sites. Indeed, the mouse and human Xi often ...
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Cross-species genomic and epigenomic landscape of retinoblastoma
... of mouse and human retinoblastomas, we ran the agreement of differential expression (AGDEX) analysis using tumor and normal retina gene expression array data ...the mouse comparison and human comparison for ...
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