1.The Function of SeMNPV IAP3 in Mammalian Cells
Lina ZHU ; Chunlei MEI ; Zhongxin ZHANG
Virologica Sinica 2008;23(3):183-188
The baculoviral inhibitors of apoptosis play a significant role in infectivity and viral host-range, which make them potential candidates for the engineering and improvement of baculovirus insecticidal. The iap3 gene of Spodoptera exigua nucleopolyhedrovirus (SeMNPV), amplified by PCR, was 939 bp encoding IAP3. The PCR product was cloned into EcoR I/Bam H I of the plasmid pEGFP-C1. GFP was fused to the N-terminaus of IAP3 to study distribution in HEK293. It was observed that the plasmid expressing IAP3 significantly inhibited apoptosis induced by cisplatin in HEK293 cells. We conclude that the IAP3 of SeMNPV is functional in mammalian cells.
2.Prenatal diagnosis and pregnancy outcomes of 22q11.2 duplication syndrome: analysis of 8 cases.
Jin MEI ; Jiao LIU ; Min WANG ; Wen ZHANG ; Hao WANG ; Sha LU ; Chaying HE ; Chunlei JIN
Journal of Zhejiang University. Medical sciences 2019;48(4):429-433
OBJECTIVE:
To investigate the relationship between 22q11.2 duplication and clinical phenotype.
METHODS:
Eight fetuses with 22q11.2 duplication syndrome diagnosed by chromosome microarray analysis (CMA) through amniocentesis from February 2015 to March 2017 were enrolled in the study. The prenatal diagnostic indications, fetal ultrasound, chromosome karyotype, peripheral blood CMA results of parents, pregnancy outcomes and follow-up of postnatal growth and development were retrospectively analyzed.
RESULTS:
Prenatal serological screening indicated 6 cases with high risk of trisomy 21, 1 case with nuchal fold (NF) thickening and 1 case of maternal chromosomal balanced translocation. Fetal ultrasonography showed 1 case of NF thickening, 1 case of fetal cerebral ventriculomegaly and 6 cases with normal ultrasound. CMA demonstrated that the size of duplication was between 651 kb and 3.26 Mb, and 22q11.2 duplication. Parents' CMA results revealed that 6 cases inherited from one of the parents with normal phenotype, and the parents of 2 cases refused the CMA test. Two couples chose induced labor; 6 cases of continued pregnancy had normal phenotypes at birth. All 6 cases were followed up with longest of 3.5 years. The growth and psychological development were normal in 5 cases, and one case was growth retardation.
CONCLUSIONS
There were no specific clinical phenotypes in 22q11.2 duplication syndrome, and most of them were inherited from one parent who has normal phenotype.
Abnormalities, Multiple
;
diagnosis
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genetics
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Chromosome Duplication
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genetics
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Chromosomes, Human, Pair 22
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genetics
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DiGeorge Syndrome
;
diagnosis
;
genetics
;
Female
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Humans
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Male
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Pregnancy
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Pregnancy Outcome
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Prenatal Diagnosis
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Retrospective Studies
3. Disease burden and quality of life in patients with psoriasis: an internet-based questionnaire survey
Xiaolan CHEN ; Liying ZHENG ; Hao ZHANG ; Jianzhong ZHANG ; Chunlei ZHANG ; Mei JU ; Jun GU ; Hongzhong JIN ; Luwen SHI ; Sheng HAN
Chinese Journal of Dermatology 2019;52(11):791-795
Objective:
To investigate direct and indirect economic burden, psychological impact, and quality of life in patients with psoriasis.
Methods:
Patients with psoriasis were recruited nationwide from "the psoriasis patient mutual assistance network" , a WeChat official account of "psoriasis patient mutual assistance platform" , and WeChat groups of psoriasis patients in different regions between July and September in 2018. An internet-based online questionnaire survey was carried out on these patients by using a self-designed questionnaire and Dermatology Life Quality Index (DLQI) scale. Comparison of enumeration data was carried out by using chi-square test, and comparison of measurement data by using Mann-Whitney