Chromosome 9
Heteromorphic variants of chromosome 9
... the chromosome 9 heteromorphic patterns with ...the chromosome 9 variant was ...marker chromosome (sSMC) there is, at least in parts, a yet unknown reason for an ascertainment bias: ...
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Identification of the Plasmodium berghei resistance locus 9 linked to survival on chromosome 9
... Survival was the most robust resistance trait that dis- tinguished the different mouse strains. While a resolving phenotype as observed previously in DBA/2J mice, could not be reproduced [38,45], a bimodal survival ...
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De Novo Pericentric Inversion of Chromosome 9 in Congenital Anomaly
... of chromosome 9 is one of the most common structural balanced chromosomal variations and has been found in both normal populations and patients with various abnormal phenotypes and ...
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Genetic and physical mapping of the short arm of human chromosome 9
... of chromosome 9 is involved in a number of genetic conditions (see Table ...of chromosome 9 with a minimum region of overlap at band 9p22 are frequently observed in acute lymphoblastic ...
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Comparative mapping of loci from human chromosome 9 in the laboratory mouse
... human chromosome 9 (HS A9) is the subject of a number of intensive positional cloning ...involving chromosome 9 (reviewed in Povey et a i , 1994; see discussion section ...mouse ...
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CONSERVED LINKAGE WITHIN A 4-cM REGION OF MOUSE CHROMOSOME 9 AND HUMAN CHROMOSOME 11
... MEISLER, 1982 Linkage of the structural gene for uroporphyrinogen I synthase to markers on mouse chromosome 9 in a cross between feral and inbred mice.. Localization of th[r] ...
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Production and Characterization of Maize Chromosome 9 Radiation Hybrids Derived From an Oat-Maize Addition Line
... maize chromosome addition lines of oat may be used ation-induced chromosome breakage in somatic cell hy- for other ...maize chromosome 9 addition line to show that maize A high-resolution ...
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Complex Structure of Knob DNA on Maize Chromosome 9: Retrotransposon Invasion into Heterochromatin
... L.) chromosome addition lines of oat (Avena sativa ...maize chromosome addition lines revealed that 180-bp repeats found in knobs are present in each of these maize chromosomes, but the copy number varies ...
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TRANSLOCATIONS IN MAIZE INVOLVING CHROMOSOME 9
... Since most of the linkage tests with genes from chromosome 9 were made involving the same genes in the same linkage order, the summarized data have been combined in a fe[r] ...
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Relationship between chromosome 9 of maize and wheat homeologous group 7 chromosomes.
... long arm of the linkage map of maize chromosome 9, and the wheat homeologous group 7 chromosomes, while a major segment of the linkage map of the long arm of maize chromo[r] ...
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Genetic Evidence of Mutator-Induced Deletions in the Short Arm of Chromosome 9 of Maize
... Albino plants are expected in the progeny of the cross of a wd heterozygote and a plant carrying a putative deletion for the wd region of the short arm of chromosome 9 (see[r] ...
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Deletions of the derivative chromosome 9 occur at the time of the Philadelphia translocation and provide a powerful and independent prognostic indicator in chronic myeloid leukemia
... Patients with CML display considerable clinical heterogeneity during the chronic phase of the disease, with some individuals progressing rapidly to blast crisis and death, whereas others remain well controlled for many ...
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Genetic evidence of Mutator-induced deletions in the short arm of chromosome 9 of maize. II. wd deletions.
... Because the wd deletions, by definition (MCCLINTOCK 1944), involve the yg2 locus, yellow-green seedlings result when the deletions are heterozygous with the yg2 allele. If wd-Mu [r] ...
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Quantitative Trait Locus Analysis of Atherosclerosis in an Intercross Between C57BL/6 and C3H Mice Carrying the Mutant Apolipoprotein E Gene
... rotic lesion size (Figure 2). Details of the QTL detected, including peak marker locus, LOD score, SI, variance, P-value, and allele conferring the trait, are presented in Table 1. The interval mapping graph for ...
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Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion
... to chromosome 9. The underlying genetic cause of chromosome 9linked FTD and ALS was recently identified [15,16], and the mutation is an expansion of a hexanucleotide repeat (GGGGCC) in a noncoding ...
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Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini review
... The clinical phenotype of C9ORF72 mutation often presents as bvFTD or ALS or FTD co-morbidities ALS. In patients with bvFTD, C9ORF72 mutation is more common than MAPT or PGRN. Anxiety or agitation, and memory dysfunction ...
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Constitutional chromothripsis involving the critical region of 9q21.13 microdeletion syndrome
... FISH analysis using Satellite Enumeration Probes (Krea- tech Diagnostics, Amsterdam, NL) and bacterial artificial chromosome probes (BAC) were done according to stand- ard procedures. The BAC probes were selected ...
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APPLICATION OF THE OVARIAN TERATOMA MAPPING METHOD IN THE MOUSE
... --To assess the accuracy of the ovarian teratoma mapping method, we compared the recombination frequency obtained for the Mpi-l- Mod-1 interval on chromosome 9 usin[r] ...
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Vol 26, No 4 (2013)
... – chromosome 9 open reading frame 72; CBS – corticobasal syndrome; FTD-ALS – frontotemporal dementia associated with amyotrophic lateral sclerosis; FTLD – frontotemporal lobar degeneration; FUS – fused in ...
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QTL analysis for chalkiness of rice and fine mapping of a candidate gene for qACE9
... RIL and 9311, qACE9, a new major QTL for the area of chalky endosperm (ACE), was fine mapped within 22 kb physical interval on chromosome 9. One candidate gene, OsAPS1, whose product reported involved in ...
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