1.Preliminary research on industrialized breeding technology system of Pinellia ternata
Xiaowei ZHANG ; Xiaofeng WANG ; Changhua ZHOU ; Xingcui ZHANG
Chinese Traditional and Herbal Drugs 1994;0(03):-
Objective Industrialized breeding technology system will be established to achieve the rapid multiplication of Pinellia ternata and to settle the problem of degeneration caused by seeds. MethodsExplant induction and effects of plant growth regulator dosage, illumination, and subculture cycle on fasciculated shoot propagation were studied. ResultsIt is good for the explant induction on medium MS+6-BA (4-5) mg/L+NAA 0.2 mg/L. P.ternata grows well under the circumstance of NAA 0.2 mg/L+6-BA 2 mg/L, double or more shoots. ConclusionIndustrialized breeding technology system of P.ternata can make its propagation rapid and support an effective way for resources preserving and sustainable utilization.
2.Quality difference of wild Lysimachiae Herba in the source areas of Sichuan, Chongqing and Guizhou
Han LIAN ; Guanglu HU ; Xiangyou TANG ; Xiaoyu YANG ; Xi WEI ; Xingcui ZHANG ; Kaizhi HU
International Journal of Traditional Chinese Medicine 2023;45(1):67-73
Objective:To determine the contents of quercetin, kaempferol, total flavonoids and extracts in 52 samples of Lysimachiae Herba collected from different origins; To analyze the quality differences of Lysimachiae Herba among different producing areas. Methods:The quercetin and kaempferol contents of the Lysimachiae Herba from Guizhou Province, Sichuan Province and Chongqing were determined by HPLC, and the total flavonoids were determined by Symergy HTX microplate reader. Results:The total content of quercetin and kaempferol in 52 samples was among 0.146 2-2.517 0 mg/g, with an average content of 0.872 6 mg/g, among which the average content of Sichuan was 1.073 2 mg/g, that of Guizhou was 0.705 4 mg/g, and that of Chongqing was 0.865 1 mg/g. Among them, 20 samples reached the standard of the Chinese Pharmacopoeia. The average content of the samples that met the standard was 1.439 7 mg/g. The compliance rate of samples collected in Guizhou, Sichuan and Chongqing reached 12.5%, 62.5%, and 38.8% respectively. The total flavonoid content of 52 samples was among 0.994 2- 3.866 4 mg/g, and 52 samples were in conformity with the ethanol hot extract standard of the Chinese Pharmacopoeia. Conclusions:The total contents of quercetin and kaempferol from different sources in Sichuan, Guizhou and Chongqing are quite different, and the total contents of quercetin and kaempferol collected from the same district and county are also quite different, and the compliance rate is low. There are great differences in total flavonoids in different producing areas and different populations of Lysimachiae Herba samples collected in the field.
3.Molecular cytogenetic diagnosis of a case with ring chromosome 18 syndrome.
Yuqiang LYU ; Xingcui WANG ; Kaihui ZHANG ; Min GAO ; Jian MA ; Xuemei LIU ; Zhongtao GAI ; Yi LIU
Chinese Journal of Medical Genetics 2019;36(10):1010-1014
OBJECTIVE:
To explore the genetic basis for a child with developmental delay and congenital syndactyly.
METHODS:
G-banding chromosomal karyotyping and chromosomal microarray analysis (CMA) were performed on peripheral blood sample from the child.
RESULTS:
The child was ascertained as 46, XY, r(18)[52]/45,XY,?18[3]. A 18q21.32-q23 deletion was identified by CMA with a size of 19.85 Mb, which has encompassed 99 genes including CTDP1, TXNL4A, TSHZ1, PIGN, RTTN, TNFRSF11A, KDSR and CYB5A.
CONCLUSION
Clinical phenotype of the patient with ring chromosome 18 is associated with the size of the euchromatin loss and involved genes. As a useful complement to conventional karyotyping, CMA has provided an powerful tool for delineating complex chromosomal aberrations.
Child
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Chromosome Aberrations
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Chromosomes, Human, Pair 18
;
genetics
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Cytogenetics
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Developmental Disabilities
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genetics
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Humans
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Karyotyping
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Ring Chromosomes
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Syndactyly
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genetics
4. Molecular cytogenetic diagnosis of a case with ring chromosome 18 syndrome
Yuqiang LYU ; Xingcui WANG ; Kaihui ZHANG ; Min GAO ; Jian MA ; Xuemei LIU ; Zhongtao GAI ; Yi LIU
Chinese Journal of Medical Genetics 2019;36(10):1010-1014
Objective:
To explore the genetic basis for a child with developmental delay and congenital syndactyly.
Methods:
G-banding chromosomal karyotyping and chromosomal microarray analysis (CMA) were performed on peripheral blood sample from the child.
Results:
The child was ascertained as 46, XY, r(18)[52]/45, XY, ? 18[3]. A 18q21.32-q23 deletion was identified by CMA with a size of 19.85 Mb, which has encompassed 99 genes including