Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus ass...

by Ya-Lien Hsueh, Yi-Ning Su, Hsin-Yu Lin, Chien-Nan Lee, Jin-Chung Shih
Published 2015-08-01

Genome-Wide Investigation of Spliceosomal SM/LSM Genes in Wheat (<i>Triticum aestivum</i> L.) and Its Progenitors

by Ruiting Gao, Ning Su, Wenqiu Pan, Qiaoyu Bao, Zhen Li, Xiaojun Nie, Wei Tong, Weining Song
Published 2021-07-01

Carving out OPE space and precise O(2) model critical exponents

by Shai M. Chester, Walter Landry, Junyu Liu, David Poland, David Simmons-Duffin, Ning Su, Alessandro Vichi
Published 2020-06-01

The relationship of neuroimaging findings and neuropsychiatric comorbidities in children with tuberous sclerosis complex

by Cheng-Hsien Huang, Steven Shinn-Forng Peng, Wen-Chin Weng, Yi-Ning Su, Wang-Tso Lee
Published 2015-09-01

Mechanisms of early- and late-feathering in Qingyuan partridge chickens

by Li Ning Su, Hua Li, Shu Wen Tan, Gui Jun Fang, Hui Yu, Ya Lan Yang
Published 2019-01-01

Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II

by Chih-Ping Chen, Yi-Ning Su, Fang-Yu Hung, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Published 2012-06-01

Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II

by Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Published 2012-06-01

Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome

by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Published 2013-03-01

Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: Prenatal diagnosis and literature review

by Chih-Ping Chen, Yi-Ning Su, Tzu-Hung Lin, Tung-Yao Chang, Jun-Wei Su, Wayseen Wang
Published 2013-12-01

Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene

by Chih-Ping Chen, Yi-Ning Su, Yu-Ting Chen, Wen-Lin Chen, Lee James Hsu, Wayseen Wang
Published 2011-09-01

Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism

by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Published 2013-03-01

Proteomics analysis of the protective effect of canola (Brassica campestris L.) bee pollen flavonoids on the tert-butyl hydroperoxide-induced EA.hy926 cell injury model

by Yue Yang, Ming-chang Liu, He Li, Yan-ge Yang, Ning Su, Ya-jun Wu, Hong Wang
Published 2020-12-01

Prenatal diagnosis of proximal femoral focal deficiency: A case report and literature review

by Tzu-Hung Lin, Chi-Hsien Chung, Jin-Chung Shih, Chia-Hui Lin, Chien-Nan Lee, Yi-Ning Su
Published 2013-06-01

X-linked Myotubular Myopathy with a Novel MTM1 Mutation in a Taiwanese Child

by Chia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, Chih-Kuang Chuang, Che-Sheng Ho, Yi-Ning Su
Published 2008-12-01

Cyclic Deformation and Correspondent Crack Initiation at Low-Stress Amplitudes in Mg–Gd–Y–Zr Alloy

by Chao He, Yujuan Wu, Liming Peng, Ning Su, Xue Li, Kun Yang, Yongjie Liu, Shucheng Yuan, Renhui Tian
Published 2018-11-01

Manifesting Pediatric Carrier of Isolated Dystrophinopathy with Initial Presentation of Myalgia and Persistent HyperCKemia

by Chien-Hua Wang, Wen-Chen Liang, Yi-Ning Su, Wen-Chieh Lee, Ching-Chyuan Su, Yuh-Jyh Jong
Published 2012-12-01

Intraperitoneal and intracardiac transfusion of recurrent fetal erythroblastosis due to anti-M alloimmunization with unfavorable outcome

by Tzu-Hung Lin, Jin-Chung Shih, Chia-Hui Lin, Shin-Yu Lin, Yi-Ning Su, Chien-Nan Lee
Published 2012-06-01

Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene

by Xue Gao, Shi–Wei Qiu, Wei-Qian Wang, Dong-Yang Kang, Ning Su, Pu Dai, Yong–Yi Yuan
Published 2021-05-01

Enrichment of leukocytes in peripheral blood using 3D printed tubes.

by Li-Fang Guo, Liu Wang, Sai Ren, Ning Su, Kun Wei, Xian-Ge Sun, Xiao-Dong Ren, Qing Huang
Published 2021-01-01

Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction

by Chih-Ping Chen, Chin-Yuan Hsu, Yi-Ning Su, Tao-Yeuan Wang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Published 2013-03-01