WU, Lingqian : rechercher sur Z-Library

Le plus grand référentiel d'articles scientifiques au monde. 70,000,000+ d'articles gratuitement.

Don't use scam websites

Livres
Articles (107)
Les plus populaires
Liste
- Liste
- Tableau

1

Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposis

Zhang, Shujie, Qin, Haisong, Lv, Weigang, Luo, Shiyu, Wang, Jin, Fu, Chunyun, Ma, Ruiyu, Shen, Yiping, Chen, Shaoke, Wu, Lingqian

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 1.02 MB

english, 2015

2

Efficient conversion of microcrystalline cellulose to 1,2-alkanediols over supported Ni catalysts

Wang, Xicheng, Meng, Lingqian, Wu, Feng, Jiang, Yijun, Wang, Lei, Mu, Xindong

Journal:

Green Chemistry

Année:

2012

Langue:

english

Fichier:

PDF, 288 KB

english, 2012

3

A father and son with mental retardation, a characteristic face, inv(12), and insertion trisomy 12p12.3-p11.2

Desheng Liang, Lingqian Wu, Qian Pan, Naoki Harada, Zhigao Long, Kun Xia, Koh-ichiro Yoshiura, Heping Dai, Norio Niikawa, Fang Cai, Jiahui Xia

Journal:

American Journal of Medical Genetics Part A

Année:

2006

Langue:

english

Fichier:

PDF, 275 KB

english, 2006

4

An Xp21.3p11.4 duplication observed in a boy with intellectual deficiency and speech delay and his asymptomatic mother

Wu, Lingqian, Liu, Jing, Lv, Weigang, Wen, Juan, Xia, Yan, Liang, Desheng

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Année:

2013

Langue:

english

Fichier:

PDF, 913 KB

english, 2013

5

PMP22 -Related neuropathies and other clinical manifestations in Chinese han patients with charcot-marie-tooth disease type 1

Zhan, Yajing, Zi, Xiaohong, Hu, Zhengmao, Peng, Ying, Wu, Lingqian, Li, Xiaobo, Jiang, Mingming, Liu, Lei, Xie, Yongzhi, Xia, Kun, Tang, Beisha, Zhang, Ruxu

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 1.46 MB

english, 2015

6

Novel de novo nonsense mutation of the PHEX gene (p.Lys50Ter) in a Chinese patient with hypophosphatemic rickets

Huang, Yanru, Mei, Libin, Pan, Qian, Tan, Hu, Quan, Yi, Gui, Baoheng, Chang, Jiazhen, Ma, Ruiyu, Peng, Ying, Yang, Pu, Liang, Desheng, Wu, Lingqian

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 956 KB

english, 2015

7

[IEEE 2015 28th IEEE International Conference on Micro Electro Mechanical Systems (MEMS) - Estoril, Portugal (2015.1.18-2015.1.22)] 2015 28th IEEE International Conference on Micro Electro Mechanical Systems (MEMS) - Bonding-friendly pcPDMS: Depositing Parylene C into PDMS matrix at an elevated temperature

Liu, Yaoping, Zhang, Lingqian, Wang, Wei, Wu, Wengang

Année:

2015

Langue:

english

Fichier:

PDF, 1.15 MB

english, 2015

8

Restraining non-specific adsorption of protein using Parylene C-caulked polydimethylsiloxane

Liu, Yaoping, Zhang, Lingqian, Wu, Wengang, Zhao, Meiping, Wang, Wei

Journal:

Biomicrofluidics

Année:

2016

Langue:

english

Fichier:

PDF, 1.37 MB

english, 2016

9

Eight-Shaped Hatching Increases the Risk of Inner Cell Mass Splitting in Extended Mouse Embryo Culture

Yan, Zheng, Liang, Hongxing, Deng, Li, Long, Hui, Chen, Hong, Chai, Weiran, Suo, Lun, Xu, Chen, Kuang, Yanping, Wu, Lingqian, Lu, Shengsheng, Lyu, Qifeng, Knott, Jason Glenn

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 1.15 MB

english, 2015

10

Paired CRISPR/Cas9 Nickases Mediate Efficient Site-Specific Integration of F9 into rDNA Locus of Mouse ESCs

Wang, Yanchi, Zhao, Junya, Duan, Nannan, Liu, Wei, Zhang, Yuxuan, Zhou, Miaojin, Hu, Zhiqing, Feng, Mai, Liu, Xionghao, Wu, Lingqian, Li, Zhuo, Liang, Desheng

Journal:

International Journal of Molecular Sciences

Année:

2018

Langue:

english

Fichier:

PDF, 20.17 MB

english, 2018

11

Next generation sequencing identified two novel mutations in NIPBL and a frame shift mutation in CREBBP in three Chinese children

Tang, Hui, Guo, Jing, Linpeng, Siyuan, Wu, Lingqian

Journal:

Orphanet Journal of Rare Diseases

Année:

2019

Langue:

english

Fichier:

PDF, 3.60 MB

english, 2019

12

Pre- and postnatal overgrowth in a patient with proximal 4p deletion

Lingqian Wu, Zhigao Long, Desheng Liang, Naoki Harada, Qian Pan, Koh-ichiro Yoshiura, Kun Xia, Heping Dai, Norio Niikawa, Jiahui Xia

Journal:

American Journal of Medical Genetics Part A

Année:

2008

Langue:

english

Fichier:

PDF, 102 KB

english, 2008

13

A ZRS duplication causes syndactyly type IV with tibial hypoplasia

Lingqian Wu, Desheng Liang, Norio Niikawa, Fen Ma, Miao Sun, Qian Pan, Zhigao Long, Zhongmin Zhou, Koh-ichiro Yoshiura, Hua Wang, Daisuke Sato, Gen Nishimura, Heping Dai, Xue Zhang, Jiahui Xia

Journal:

American Journal of Medical Genetics Part A

Année:

2009

Langue:

english

Fichier:

PDF, 191 KB

english, 2009

14

A patient with apparently reciprocal translocation and cryptic 10p deletion

Lingqian Wu, Xi Liao, Hua Wang, Zhongmin Zhou, Weigang Lv, Desheng Liang

Journal:

American Journal of Medical Genetics Part A

Année:

2011

Langue:

english

Fichier:

PDF, 8.23 MB

english, 2011

15

A family with partial duplication/deletion 4p due to a balanced t (4; 15) (p16.2; p11.2) translocation

Lingqian Wu, Dahua Meng, Zhongmin Zhou, Juan Du, Zhigao Long, Desheng Liang

Journal:

American Journal of Medical Genetics Part A

Année:

2011

Langue:

english

Fichier:

PDF, 412 KB

english, 2011

16

Expression of reconstructive hFVIII in the hrDNA by using hrDNA targeting vector

Xionghao Liu, Mujun Liu, She Hua, Wen Lu, Zhigang Xue, Desheng Liang, Fang Cai, Qian Pan, Zhigao Long, Lingqian Wu, Heping Dai, Kun Xia, Jiahui Xia

Journal:

Chinese Science Bulletin

Année:

2005

Langue:

english

Fichier:

PDF, 1.03 MB

english, 2005

17

Silica nanoparticle is a possible safe carrier for gene therapy

Zhigang Xue, Desheng Liang, Yumei Li, Zhigao Long, Qian Pan, Xionghao Liu, Lingqian Wu, Shaihong Zhu, Fang Cai, Heping Dai, Baisha Tang, Kun Xia, Jiahui Xia

Journal:

Chinese Science Bulletin

Année:

2005

Langue:

english

Fichier:

PDF, 2.24 MB

english, 2005

18

A syndactyly type IV locus maps to 7q36

Daisuke Sato, Desheng Liang, Lingqian Wu, Qian Pan, Kun Xia, Heping Dai, Hua Wang, Gen Nishimura, Koh-Ichiro Yoshiura, Jiahui Xia, Norio Niikawa

Journal:

Journal of Human Genetics

Année:

2007

Langue:

english

Fichier:

PDF, 190 KB

english, 2007

19

Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a uniqueSLC26A4mutation spectrum

Hao Hu, Lingqian Wu, Yong Feng, Qian Pan, Zhigao Long, Juan Li, Heping Dai, Kun Xia, Desheng Liang, Norio Niikawa, Jiahui Xia

Journal:

Journal of Human Genetics

Année:

2007

Langue:

english

Fichier:

PDF, 160 KB

english, 2007

20

A new processing method for theAEindex

LingQian Zhang, ZhenXing Liu, ZhiWei Ma, W. Baumjohann, Jian Wu, M. Dunlop, JianKui Shi, Li Lu, JiYe Wang

Journal:

Science China Technological Sciences

Année:

2008

Langue:

english

Fichier:

PDF, 759 KB

english, 2008

21

Investigation of hrDNA targeting vector-mediated tumor-specific suicide gene therapy for hepatocellular carcinoma

Lina Wang, Zhigang Xue, Zhuo Li, Jinfeng Xue, Xionghao Liu, Qian Pan, Zhigao Long, Fang Cai, Lingqian Wu, Heping Dai, Kun Xia, Desheng Liang, Jiahui Xia

Journal:

Chinese Science Bulletin

Année:

2006

Langue:

english

Fichier:

PDF, 3.74 MB

english, 2006

22

A novel fusion suicide gene yeast CDglyTK plays a role in radio-gene therapy of nasopharyngeal carcinoma

Xia, Kun, Liang, Desheng, Tang, Aifa, Feng, Yong, Zhang, Junyi, Pan, Qian, Long, Zhigao, Dai, Heping, Cai, Fang, Wu, Lingqian

Journal:

Cancer Gene Therapy

Année:

2004

Langue:

english

Fichier:

PDF, 193 KB

english, 2004

23

Three patients with Wolf-Hirschhorn syndrome carrying a satellited chromosome 4p

Desheng Liang, Zhongmin Zhou, Dahua Meng, Juan Du, Juan Wen, Norio Niikawa, Lingqian Wu

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Année:

2012

Langue:

english

Fichier:

PDF, 929 KB

english, 2012

24

Novel compound heterozygous mutation of MLYCD in a Chinese patient with malonic aciduria

Jinjie Xue, Jing Peng, Mingxing Zhou, Le Zhong, Fei Yin, Desheng Liang, Lingqian Wu

Journal:

Molecular Genetics and Metabolism

Année:

2012

Langue:

english

Fichier:

PDF, 585 KB

english, 2012

25

Mutation Analysis in Chinese Patients with Cornelia de Lange Syndrome

Zhong, Qiulian, Liang, Desheng, Liu, Jing, Xue, Jinjie, Wu, Lingqian

Journal:

Genetic Testing and Molecular Biomarkers

Année:

2012

Langue:

english

Fichier:

PDF, 234 KB

english, 2012

26

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing

Liang, Desheng, Lv, Weigang, Wang, Hua, Xu, Liangpu, Liu, Jing, Li, Haoxian, Hu, Liang, Peng, Ying, Wu, Lingqian

Journal:

Prenatal Diagnosis

Année:

2013

Langue:

english

Fichier:

PDF, 260 KB

english, 2013

27

Mutation analysis of the SRY, NR5A1 , and DHH genes in six Chinese 46,XY women

Liao, Xi, Liang, Desheng, Li, Yanping, Xi, Hui, Quan, Yi, Wu, Lingqian

Journal:

Journal of Maternal-Fetal and Neonatal Medicine

Année:

2011

Langue:

english

Fichier:

PDF, 689 KB

english, 2011

28

Identification of MicroRNAs in Human Follicular Fluid: Characterization of MicroRNAs That Govern Steroidogenesis in Vitro and Are Associated With Polycystic Ovary Syndrome in Vivo

Sang, Qing, Yao, Zhongyuan, Wang, Huan, Feng, Ruizhi, Wang, Haojue, Zhao, Xinzhi, Xing, Qinghe, Jin, Li, He, Lin, Wu, Lingqian, Wang, Lei

Journal:

Journal of Clinical Endocrinology & Metabolism

Année:

2013

Langue:

english

Fichier:

PDF, 582 KB

english, 2013

29

Phenotypic expansion of the interstitial 16p13.3 duplication: A case report and review of the literature

Li, Zhuo, Liu, Jing, Li, Haoxian, Peng, Ying, Lv, Weigang, Long, Zhigao, Liang, Desheng, Wu, Lingqian

Journal:

Année:

2013

Langue:

english

Fichier:

PDF, 577 KB

english, 2013

30

TALE nickase mediates high efficient targeted transgene integration at the human multi-copy ribosomal DNA locus

Wu, Yong, Gao, Tieli, Wang, Xiaolin, Hu, Youjin, Hu, Xuyun, Hu, Zhiqing, Pang, Jialun, Li, Zhuo, Xue, Jinfeng, Feng, Mai, Wu, Lingqian, Liang, Desheng

Journal:

Biochemical and Biophysical Research Communications

Année:

2014

Langue:

english

Fichier:

PDF, 1.48 MB

english, 2014

31

Copy Number Variation Sequencing for Comprehensive Diagnosis of Chromosome Disease Syndromes

Liang, Desheng, Peng, Ying, Lv, Weigang, Deng, Linbei, Zhang, Yanghui, Li, Haoxian, Yang, Pu, Zhang, Jianguang, Song, Zhuo, Xu, Genming, Cram, David S., Wu, Lingqian

Journal:

The Journal of Molecular Diagnostics

Année:

2014

Langue:

english

Fichier:

PDF, 1.45 MB

english, 2014

32

Effective TiO2 hybrid heterostructure fabricated on nano mesoporous phenolic resol for visible-light photocatalysis

Jiang, Yijun, Meng, Lingqian, Mu, Xindong, Li, Xiutao, Wang, Haisong, Chen, Xiufang, Wang, Xicheng, Wang, Wei, Wu, Feng, Wang, Xiaoyan

Journal:

Journal of Materials Chemistry

Année:

2012

Langue:

english

Fichier:

PDF, 675 KB

english, 2012

33

Design of a Microchannel-Nanochannel-Microchannel Array Based Nanoelectroporation System for Precise Gene Transfection

Gao, Keliang, Li, Lei, He, Lingna, Hinkle, Kevin, Wu, Yun, Ma, Junyu, Chang, Lingqian, Zhao, Xi, Perez, Daniel Gallego, Eckardt, Sigrid, Mclaughlin, John, Liu, Boyu, Farson, Dave F., Lee, L. James

Journal:

Année:

2014

Langue:

english

Fichier:

PDF, 2.04 MB

english, 2014

34

Brief report adult patient presenting an interstitial (9) (q21.32q31.1) direct duplication resulting from the malsegregation of a paternal balanced insertional translocation

Deng, Linbei, Peng, Ying, Liu, Jing, Wen, Juan, Xia, Yan, Liang, Desheng, Wu, Lingqian

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Année:

2014

Langue:

english

Fichier:

PDF, 227 KB

english, 2014

35

Two novel NIPBL gene mutations in Chinese patients with Cornelia de Lange syndrome

Mei, Libin, Liang, Desheng, Huang, Yanru, Pan, Qian, Wu, Lingqian

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 1009 KB

english, 2015

36

Magnetic Tweezers-Based 3D Microchannel Electroporation for High-Throughput Gene Transfection in Living Cells

Chang, Lingqian, Howdyshell, Marci, Liao, Wei-Ching, Chiang, Chi-Ling, Gallego-Perez, Daniel, Yang, Zhaogang, Lu, Wu, Byrd, John C., Muthusamy, Natarajan, Lee, L. James, Sooryakumar, Ratnasingham

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 5.53 MB

english, 2015

37

CrypticFMR1mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report

Luo, Shiyu, Huang, Wen, Xia, Qiuping, Xia, Yan, Du, Qian, Wu, Lingqian, Duan, Ranhui

Journal:

BMC Medical Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 1.34 MB

english, 2014

38

Identification of a novelSHOXmutation in a Chinese family with isolated Madelung deformity

MEI, LIBIN, HUANG, YANRU, PAN, QIAN, LI, HAOXIAN, LIANG, DESHENG, WU, LINGQIAN

Journal:

Journal of Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 2.31 MB

english, 2014

39

Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome

Ma, Ruiyu, Peng, Ying, Zhang, Yanghui, Xia, Yan, Tang, Guizhi, Chang, Jiazhen, Guo, Ruolan, Gui, Baoheng, Huang, Yanru, Chen, Chen, Liang, Desheng, Wu, Lingqian

Journal:

Molecular Cytogenetics

Année:

2015

Langue:

english

Fichier:

PDF, 778 KB

english, 2015

40

DMD mutation spectrum analysis in 613 Chinese patients with dystrophinopathy

Guo, Ruolan, Zhu, Guosheng, Zhu, Huimin, Ma, Ruiyu, Peng, Ying, Liang, Desheng, Wu, Lingqian

Journal:

Journal of Human Genetics

Année:

2015

Langue:

english

Fichier:

PDF, 1.62 MB

english, 2015

41

Targeted next-generation sequencing identifies novel compound heterozygous mutations of DYNC2H1 in a fetus with short rib-polydactyly syndrome, type III

Mei, Libin, Huang, Yanru, Pan, Qian, Su, Wei, Quan, Yi, Liang, Desheng, Wu, Lingqian

Journal:

Clinica Chimica Acta

Année:

2015

Langue:

english

Fichier:

PDF, 903 KB

english, 2015

42

Rare intracranial cholesterol deposition and a homozygous mutation of LDLR in a familial hypercholesterolemia patient

Li, Haoxian, Zhang, Yanghui, Wei, Xianda, Peng, Ying, Yang, Pu, Tan, Hu, Chen, Chen, Pan, Qian, Liang, Desheng, Wu, Lingqian

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 1.18 MB

english, 2015

43

Nonviral Gene Targeting at rDNA Locus of Human Mesenchymal Stem Cells

Hu, Youjin, Liu, Xionghao, Long, Panpan, Xiao, Di, Cun, Jintao, Li, Zhuo, Xue, Jinfeng, Wu, Yong, Luo, Sha, Wu, Lingqian, Liang, Desheng

Journal:

BioMed Research International

Année:

2013

Langue:

english

Fichier:

PDF, 4.72 MB

english, 2013

44

3D Nanochannel Electroporation for High-throughput Cell Transfection with High Uniformity and Dosage Control

Chang, Lingqian, Bertani, Paul, Gallego-Perez, Daniel, Yang, Zhaogang, Chen, Feng, Chang, Chiling, Malkoc, Veysi, Kuang, Tairong, Gao, Keliang, Lee, L.James, Lu, Wu

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 4.17 MB

english, 2015

45

Dielectrophoresis-assisted 3D nanoelectroporation for non-viral cell transfection in adoptive immunotherapy

Chang, Lingqian, Gallego-Perez, Daniel, Zhao, Xi, Bertani, Paul, Yang, Zhaogang, Chiang, Chi-Ling, Malkoc, Veysi, Shi, Junfeng, Sen, Chandan K., Odonnell, Lynn, Yu, Jianhua, Lu, Wu, Lee, L. James

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 3.04 MB

english, 2015

46

Pachygyria, seizures, hypotonia, and growth retardation in a patient with an atypical 1.33Mb inherited microduplication at 22q11.23

Chang, Jiazhen, Zhao, Lijuan, Chen, Chen, Peng, Ying, Xia, Yan, Tang, Guizhi, Bai, Ting, Zhang, Yanghui, Ma, Ruiyu, Guo, Ruolan, Mei, Libin, Liang, Desheng, Cao, Qinying, Wu, Lingqian

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 734 KB

english, 2015

47

Clinical and molecular investigation in Chinese patients with glutaric aciduria type I

Zhang, Yanghui, Li, Haoxian, Ma, Ruiyu, Mei, Libin, Wei, Xianda, Liang, Desheng, Wu, Lingqian

Journal:

Clinica Chimica Acta

Année:

2015

Langue:

english

Fichier:

PDF, 521 KB

english, 2015

48

A novel de novo POGZ mutation in a patient with intellectual disability

Tan, Bo, Zou, Yongyi, Zhang, Yue, Zhang, Rui, Ou, Jianjun, Shen, Yidong, Zhao, Jingping, Luo, Xiaomei, Guo, Jing, Zeng, Lanlan, Hu, Yiqiao, Zheng, Yu, Pan, Qian, Liang, Desheng, Wu, Lingqian

Journal:

Journal of Human Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 562 KB

english, 2016

49

Chromosomal analysis of blastocysts from balanced chromosomal rearrangement carriers

Gui, Baoheng, Yao, Zhongyuan, Li, Yanping, Liu, Donge, Liu, Nenghui, Xia, Yan, Huang, Yanru, Mei, Libin, Ma, Ruiyu, Lu, Sijia, Liang, Desheng, Wu, Lingqian

Journal:

Année:

2016

Langue:

english

Fichier:

PDF, 1.67 MB

english, 2016

50

A New Next-Generation Sequencing-Based Assay for Concurrent Preimplantation Genetic Diagnosis of Charcot-Marie-Tooth Disease Type 1A and Aneuploidy Screening

Gui, Baoheng, Yang, Pu, Yao, Zhongyuan, Li, Yanping, Liu, Donge, Liu, Nenghui, Lu, Sijia, Liang, Desheng, Wu, Lingqian

Journal:

Journal of Genetics and Genomics

Année:

2016

Langue:

english

Fichier:

PDF, 979 KB

english, 2016