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南京农业大学农学院《Plant Physiology》发表管荣展课题组“A small chromosomal inversion mediated by MITEs confers cleistogamy in Brassica napus”（图）
管荣展 作物遗传 育种
2023/10/28
2022年9月29日，南京农业大学作物遗传与种质创新国家重点实验室油菜遗传育种团队在Plant Physiology发表了 “A small chromosomal inversion mediated by MITEs confers cleistogamy in Brassica napus”的研究论文，阐明了油菜花瓣开放与闭合行为的形成机制。
Dual-color oligo-FISH can reveal chromosomal variations and evolution in Oryza species
Oryza species chromosomal variation dual-color oligo-FISH karyotype
2023/8/9
Fluorescence in situ hybridization using probes based on oligonucleotides (oligo-FISH) is a useful tool for chromosome identification and karyotype analysis. Here we developed two oligo-FISH probes th...
Chronic Myeloid Leukemia with Variant Chromosomal Translocations:Results of Treatment with Imatinib Mesylate
Chronic myeloid leukemia Imatinib Variant translocation
2015/7/10
Objective: To evaluate the efficacy of imatinib in chronic myeloid leukemia patients with variant translocations. Methods: Forty eight chronic myeloid leukemia patients carrying variant translocations...
Hypodiploidy as a prominent attributor to chromosomal aneuploidy in transgenic rabbit embryos
chromosomal aneuploidy EGFP embryo hFVIII rabbit transgenic
2015/6/5
Transgenic animals play a vital role in basic research, agriculture and pharmaceutical industries. Rabbits have the advantage of other large laboratory species in that they have a short gestation peri...
Molecular Characterization, Chromosomal Localizations, Expression Profile, and Association Analysis of the Porcine PECI Gene with Carcass Traits
Full-length cDNA RH Mapping Significant Association Backfat Thickness PECI Gene Pigs
2016/5/3
The full-length cDNA of the porcine peroxisomal 3,2-enoyl-CoA isomerase (PECI) gene encodes a monofunctional peroxisomal 3,2-enoyl-CoA isomerase. Cloning and sequencing...
COMPARATIVE STUDIES OF THE CHROMOSOMAL ARRANGEMENT IN THE C-METAPHASE BETWEEN NORMAL KARYOTYPE AND TRISOMY-21
Chromosomal arrangements C-metaphase Radial & Homologue distances (+21) Satellite-association
2009/12/31
Human chromosomes in amnion cells and lymphocytes with normal karyotype and in lymphocytes with pathological karyotype (2n=47, +21) were compared as to their position in the metaphase. None of the col...
CHROMOSOMAL & CYTOGENETIC:Studies in a case of Klinefelters Syndrome
CHROMOSOMAL CYTOGENETIC:Studies Klinefelters Syndrome
2009/12/7
A 21 year old boy was first seen because of Gynecomastia and primary hypogonadisme. A biopsy specimen from the testes revealed hyalinization of the seminiferous tubules with spermatogenic arrest, and ...
The Frequency of Chromosomal Abnormalities in Men With Azoospermia and Oligoasthenoteratozoospermia: a Preliminary Study
Male infertility chromosomal abnormalities
2009/7/6
The aim of this study is to investigate the frequency of chromosomal abnormalities in men with severe andrological infertility, In 50 men with azoospermia and severe oligoasthenoteratozoospermia (OAT)...
Chromosomal Aberrations in Peripheral Lymphocytes of a High-Voltage Power Lineman Exposed to Electromagnetic Fields
Chromosomal aberrations Human peripheral lymphocytes Electromagnetic fields
2009/7/2
During the last decade, several studies have focused on the adverse effects on health caused by exposure to electromagnetic fields (EMF). Some epidemiological studies of workers exposed to EMF have sh...
Spinocerebellar Ataxia With a Novel Chromosomal Defect: Del 5q34 - A case report
Spinocerebellar ataxia inherited and cytogenetic study
2009/6/23
Spinocerebellar ataxias (SCA) are inherited through autosomal dominant, autosomal recessive, and X-linked patterns, and may be seen sporadically (1-4). Cerebellar findings are the main clinical charac...
Chromosomal Aberrations in Radiation Waste Repository Workers Detected by Fish Painting and Giemsa Staining
Occupational radiation exposure Human lymphocytes Chromosomal aberrations Fluorescent in situ hybridization
2009/6/23
We aimed to assess chromosomal aberration frequency by means of FISH chromosome painting and conventional Giemsa staining in peripheral blood lymphocytes of workers at a nuclear waste repository. The ...
The Effect of Glutathione S-transferase M1 Genotype on Benzo[a]pyrene-Induced Sister Chromatid Exchanges and Chromosomal Aberrations in Peripheral Blood Lymphocytes
Department of Medical Biology,Cerrahpaş a Faculty of Medicine,University of İ stanbul,İ stanbul-Turkey
2009/6/23
Sister chromatid exchange (SCE) and chromosomal aberration (CA) in peripheral lymphocytes have been widely used in assessing exposure to mutagens and carcinogens. One of the extensively studied genoto...
Seckel Syndrome with Spontaneous Chromosomal Instability
Seckel syndrome chromosomal instability chromosomal breakage syndrome
2009/6/16
Seckel syndrome is an autosomal recessive disorder characterized by prenatal and postnatal growth retardation, bird-headed face and mild mental retardation. It is a disorder involving the DNA damage-r...
Expression Characterization, Polymorphism and Chromosomal Location of the Porcine Calsarcin-3 Gene
Expression Localization Polymorphism Calsarcin-3 Porcine
2016/5/3
Calcineurin is a calmodulin dependent protein that functions as a regulator of muscle cell growth and function. Agents capable of interacting with calcineurin could have important applications in musc...
Detection of Hemizygous Chromosomal Copy Number Variants in Williams-Beuren Syndrome (WBS) by Duplex Quantitative PCR Array: An Unusual Type of WBS Genetic Defect
human chromosome 7 deletion copy number variants genome
2009/4/14
We have developed a dual probe quantitative PCR (qPCR) mini array enabling a more accurate analysis of the relationship between copy number variants (CNVs) and other genomic features in specific areas...