نتایج جستجو برای: disomic addition lines

تعداد نتایج: 908139  

D. Kor, J. M. Panandam, M. J. Taghavi, M. Moghim, M. Pourkazemi, S. G. Tan, S. S. Siraj,

Understanding the scale at which wild stocks of Persian sturgeon (Acipenser persicus) are genetically discrete is necessary for effective management of this commercially important species. Disomic DNA microsatellite markers are among the best tools for determining stock structure in fishes. As all sturgeon species have a polyploid ancestry of all sturgeons, most gene loci exhibit more than two ...

Journal: :Forests 2021

Diploid clones of the hybrid acacia (Acacia mangium × A. auriculiformis) are widely planted in Vietnam because their high productivity, adaptability, and commercial wood yields. Polyploid breeding offers possibilities for further enhancing vigor generating new value genotypes. In a field trial, we compared three diploid with respective colchicine-induced tetraploid lines. Flowering seed product...

2015
Xiaofei Yang Changyou Wang Xin Li Chunhuan Chen Zengrong Tian Yajuan Wang Wanquan Ji Aimin Zhang

Leymus mollis (2n = 4x = 28, NsNsXmXm) possesses novel and important genes for resistance against multi-fungal diseases. The development of new wheat-L. mollis introgression lines is of great significance for wheat disease resistance breeding. M11003-3-1-15-8, a novel disomic substitution line of common wheat cv. 7182 -L. mollis, developed and selected from the BC1F5 progeny between wheat cv. 7...

Journal: :Genome 2006
J Li D L Klindworth F Shireen X Cai J Hu S S Xu

The aneuploid stocks of durum wheat (Triticum turgidum L. subsp. durum (Desf.) Husnot) and common wheat (T. aestivum L.) have been developed mainly in 'Langdon' (LDN) and 'Chinese Spring' (CS) cultivars, respectively. The LDN-CS D-genome chromosome disomic substitution (LDN-DS) lines, where a pair of CS D-genome chromosomes substitute for a corresponding homoeologous A- or B-genome chromosome p...

Journal: :Genetics 1977
D A Campbell S Fogel

Experiments designed to characterize the association between disomic chromosome loss and centromere-adjacent mitotic recombination were performed. Mitotic gene convertants were selected at two heteroallelic sites on the left arm of disomic chromosome III and tested for coincident chromosome loss. The principal results are: (1) Disomic chromosome loss is markedly enhanced (nearly 40-fold) over b...

Journal: :Genetics 1988
B Rockmill S Fogel

Mutants at a newly identified locus, DIS1 (disjunction), were detected by screening for mutants that generate aneuploid spores (chromosome VIII disomes) at an increased frequency. Strains carrying the partially dominant alleles, DIS1-1 or DIS1-2, generate disomes at rates up to 100 times the background level. Mitotic nondisjunction is also increased 10- to 50-fold over background. Half-tetrad a...

Journal: :Blood 1992
N Onodera N R McCabe C M Rubin

Hyperdiploidy with greater than or equal to 50 chromosomes is a frequent and distinct karyotypic pattern in the malignant cells of children with acute lymphoblastic leukemia. To understand better the mechanism of formation of the hyperdiploid karyotype, we studied 15 patients using 20 DNA probes that detect restriction fragment length polymorphisms. We first examined disomic chromosomes for los...

Journal: :Clinical genetics 2016
K Matsubara N Murakami M Fukami M Kagami T Nagai T Ogata

Recent studies have suggested that disomic oocyte-mediated uniparental disomy 15 (UPD(15)mat) is increased in patients with Prader-Willi syndrome (PWS) born after medically assisted reproduction (MAR). However, it remains unknown whether the increase is primarily due to MAR procedure itself or advanced maternal childbearing ages as a predisposing factor for the disomic oocyte production. To exa...

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