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TP53 alterations in relapsed childhood acute lymphoblastic leukemia.

Yu CH, Chang WT, Jou ST, Lin TK, Chang YH, Lin CY, Lin KH, Lu MY, Chen SH, Wu KH, Wang SC, Chang HH, Su YN, Hung CC, Lin DT, Chen HY, Yang YL.

Cancer Sci. 2019 Nov 14. doi: 10.1111/cas.14238. [Epub ahead of print]


Qishen capsule safely boosts cardiac function and angiogenesis via the MEK/ERK pathway in a rat myocardial infarction model.

Guo CX, Li ZY, Niu JB, Fan SC, Yan SY, Lu PP, Su YN, Ma LH.

J Geriatr Cardiol. 2019 Oct;16(10):764-774. doi: 10.11909/j.issn.1671-5411.2019.10.008.


Fragile X syndrome carrier screening in pregnant women in Chinese Han population.

Hung CC, Lee CN, Wang YC, Chen CL, Lin TK, Su YN, Lin MW, Kang J, Tai YY, Hsu WW, Lin SY.

Sci Rep. 2019 Oct 29;9(1):15456. doi: 10.1038/s41598-019-51726-4.


Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith-Wiedemann spectrum.

Lee CT, Tung YC, Hwu WL, Shih JC, Lin WH, Wu MZ, Kuo KT, Yang YL, Chen HL, Chen M, Su YN, Jong YJ, Liu SY, Tsai WY, Lee NC.

Am J Med Genet A. 2019 Sep;179(9):1878-1883. doi: 10.1002/ajmg.a.61276. Epub 2019 Jun 24.


A new Raspy Cricket from the northern Australian Rainforests (Orthoptera: Gryllacrididae).

Rentz D, Su YN, BÉthoux O.

Zootaxa. 2018 Nov 5;4514(1):41-52. doi: 10.11646/zootaxa.4514.1.3.


New lineages of Lebinthini from Australia (Orthoptera: Gryllidae: Eneopterinae).

Robillard T, Su YN.

Zootaxa. 2018 Mar 8;4392(2):241-266. doi: 10.11646/zootaxa.4392.2.2.


Changes in the nomenclature of three Australian crickets.

Rentz DCF, Su YN.

Zootaxa. 2018 Apr 17;4410(2):390-392. doi: 10.11646/zootaxa.4410.2.9.


Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan.

Lu CY, Tsao PN, Ke YY, Lin YH, Lin YH, Hung CC, Su YN, Hsu WC, Hsieh WS, Huang LM, Wu CC, Hsu CJ.

J Pediatr. 2018 Aug;199:144-150.e1. doi: 10.1016/j.jpeds.2018.02.064. Epub 2018 Apr 19.


[Clinical Trials for Treatment of Allergic Rhinitis with Heat Sensitive Moxibustion and Its Regularity of Heat-sensitization Acupoint Distribution].

Lin YF, Lu JM, Su YN, Zhong ZB, Zhang ZD.

Zhen Ci Yan Jiu. 2017 Dec 25;42(6):527-32. doi: 10.13702/j.1000-0607.2017.06.012. Chinese.


The improved growth performance and enhanced immune function by DL-methionyl-DL-methionine are associated with NF-κB and TOR signalling in intestine of juvenile grass carp (Ctenopharyngodon idella).

Su YN, Wu P, Feng L, Jiang WD, Jiang J, Zhang YA, Figueiredo-Silva C, Zhou XQ, Liu Y.

Fish Shellfish Immunol. 2018 Mar;74:101-118. doi: 10.1016/j.fsi.2017.12.051. Epub 2017 Dec 29.


Museum Genomics Confirms that the Lord Howe Island Stick Insect Survived Extinction.

Mikheyev AS, Zwick A, Magrath MJL, Grau ML, Qiu L, Su YN, Yeates D.

Curr Biol. 2017 Oct 23;27(20):3157-3161.e4. doi: 10.1016/j.cub.2017.08.058. Epub 2017 Oct 5.


Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan.

Liang WC, Tian X, Yuo CY, Chen WZ, Kan TM, Su YN, Nishino I, Wong LC, Jong YJ.

PLoS One. 2017 Aug 10;12(8):e0183406. doi: 10.1371/journal.pone.0183406. eCollection 2017.


The sFlt-1/PlGF ratio as a predictor for poor pregnancy and neonatal outcomes.

Chang YS, Chen CN, Jeng SF, Su YN, Chen CY, Chou HC, Tsao PN, Hsieh WS.

Pediatr Neonatol. 2017 Dec;58(6):529-533. doi: 10.1016/j.pedneo.2016.10.005. Epub 2017 May 10.


Early Screening and Prevention of Preeclampsia.

Lin TH, Su YN.

J Med Ultrasound. 2017 Apr-Jun;25(2):68-70. doi: 10.1016/j.jmu.2015.01.001. Epub 2017 Feb 4. No abstract available.


Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan.

Liang WC, Tian X, Yuo CY, Chen WZ, Kan TM, Su YN, Nishino I, Wong LC, Jong YJ.

PLoS One. 2017 Feb 9;12(2):e0170517. doi: 10.1371/journal.pone.0170517. eCollection 2017. Erratum in: PLoS One. 2017 Aug 10;12 (8):e0183406.


Carbetocin in prevention of postpartum hemorrhage: Experience in a tertiary medical center of Taiwan.

Chen CY, Su YN, Lin TH, Chang Y, Horng HC, Wang PH, Yeh CC, Chang WH, Huang HY.

Taiwan J Obstet Gynecol. 2016 Dec;55(6):804-809. doi: 10.1016/j.tjog.2016.07.009.


A simple and quick method of displaying liquid-preserved morphological structures for microphotography.

Su YN.

Zootaxa. 2016 Dec 21;4208(6):zootaxa.4208.6.6. doi: 10.11646/zootaxa.4208.6.6.


Laser speckle contrast imaging and Oxygen to See for assessing microcirculatory liver blood flow changes following different volumes of hepatectomy.

Li CH, Ge XL, Pan K, Wang PF, Su YN, Zhang AQ.

Microvasc Res. 2017 Mar;110:14-23. doi: 10.1016/j.mvr.2016.11.004. Epub 2016 Nov 25.


Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.

Chen CP, Ko TM, Su YN, Wang LK, Chern SR, Wu PS, Chen YN, Chen SW, Ko K, Lee CC, Chen LF, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2016 Oct;55(5):733-737. doi: 10.1016/j.tjog.2016.07.007.


Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome.

Lin HY, Chuang CK, Tu RY, Fang YY, Su YN, Chen CP, Chang CY, Liu HC, Chu TH, Niu DM, Lin SP.

Mol Genet Metab. 2016 Sep;119(1-2):8-13. doi: 10.1016/j.ymgme.2016.07.003. Epub 2016 Jul 12.


Studies in Australian Tettigoniidae: A review of the Australian katydids of the genus Goodangarkia (Tettigoniidae: Conocephalinae; Agraeciini; Liarina).

Rentz D, Su YN, Ueshima N, Wilson G.

Zootaxa. 2016 Jul 5;4136(1):71-100. doi: 10.11646/zootaxa.4136.1.3.


Newborn genetic screening for hearing impairment: a population-based longitudinal study.

Wu CC, Tsai CH, Hung CC, Lin YH, Lin YH, Huang FL, Tsao PN, Su YN, Lee YL, Hsieh WS, Hsu CJ.

Genet Med. 2017 Jan;19(1):6-12. doi: 10.1038/gim.2016.66. Epub 2016 Jun 16.


Apoptosis in response to heat stress is positively associated with heat-shock protein 90 expression in chicken myocardial cells in vitro.

Zhang XH, Wu H, Tang S, Li QN, Xu J, Zhang M, Su YN, Yin B, Zhao QL, Kemper N, Hartung J, Bao ED.

J Vet Sci. 2017 Jun 30;18(2):129-140. doi: 10.4142/jvs.2017.18.2.129.


Probable high prevalence of limb-girdle muscular dystrophy type 2D in Taiwan.

Liang WC, Chou PC, Hung CC, Su YN, Kan TM, Chen WZ, Hayashi YK, Nishino I, Jong YJ.

J Neurol Sci. 2016 Mar 15;362:304-8. doi: 10.1016/j.jns.2016.02.002. Epub 2016 Feb 2.


Aplysia Locomotion: Network and Behavioral Actions of GdFFD, a D-Amino Acid-Containing Neuropeptide.

Yang CY, Yu K, Wang Y, Chen SA, Liu DD, Wang ZY, Su YN, Yang SZ, Chen TT, Livnat I, Vilim FS, Cropper EC, Weiss KR, Sweedler JV, Jing J.

PLoS One. 2016 Jan 21;11(1):e0147335. doi: 10.1371/journal.pone.0147335. eCollection 2016.


Targeted next-generation sequencing of cancer genes identified frequent TP53 and ATRX mutations in leiomyosarcoma.

Yang CY, Liau JY, Huang WJ, Chang YT, Chang MC, Lee JC, Tsai JH, Su YN, Hung CC, Jeng YM.

Am J Transl Res. 2015 Oct 15;7(10):2072-81. eCollection 2015.


Genotype and phenotype analysis of Taiwanese patients with osteogenesis imperfecta.

Lin HY, Chuang CK, Su YN, Chen MR, Chiu HC, Niu DM, Lin SP.

Orphanet J Rare Dis. 2015 Dec 1;10:152. doi: 10.1186/s13023-015-0370-2.


Studies in Australian Katydids: A Review of the Australian Snub-nosed Sylvan katydids (Tettigoniidae; Pseudophyllinae; Simoderini).

Rentz D, Su YN, Ueshima N.

Zootaxa. 2015 Apr 8;3946(1):1-54. doi: 10.11646/zootaxa.3946.1.1. Review.


Split hand/foot malformations with microdeletions at chromosomes 7 and 19 detected using array comparative genomic hybridization.

Wu CJ, Su YN, Lin TH, Tseng LH, Chao KH.

Taiwan J Obstet Gynecol. 2015 Feb;54(1):92-4. doi: 10.1016/j.tjog.2014.01.006. No abstract available.


Prenatal diagnosis of true diphallia and associated anomalies.

Tu YA, Su YN, Yang PK, Shih JC.

Obstet Gynecol. 2014 Aug;124(2 Pt 2 Suppl 1):416-8. doi: 10.1097/AOG.0000000000000327.


Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15.

Chen CP, Chen M, Su YN, Chern SR, Wu PS, Chang SP, Kuo YL, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2014 Mar;53(1):129-32. doi: 10.1016/j.tjog.2013.12.004. No abstract available.


Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer.

Chen CP, Su YN, Chen SU, Chang TY, Wu PC, Chern SR, Wu PS, Kuo YL, Wang W.

Taiwan J Obstet Gynecol. 2014 Mar;53(1):90-4. doi: 10.1016/j.tjog.2013.12.003.


Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia.

Chen CP, Su YN, Lin MH, Wang TY, Chern SR, Kuo YL, Chen YT, Wang W.

Taiwan J Obstet Gynecol. 2014 Mar;53(1):68-73. doi: 10.1016/j.tjog.2013.10.036.


Applying the ICF-CY framework to examine biological and environmental factors in early childhood development.

Hwang AW, Liao HF, Chen PC, Hsieh WS, Simeonsson RJ, Weng LJ, Su YN.

J Formos Med Assoc. 2014 May;113(5):303-12. doi: 10.1016/j.jfma.2011.10.004. Epub 2012 May 16.


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

Huang CH, Peng SS, Weng WC, Su YN, Lee WT; National Taiwan University Hospital Tuberous Sclerosis Complex (NTUH TSC) Study Group.

J Formos Med Assoc. 2015 Sep;114(9):849-54. doi: 10.1016/j.jfma.2014.02.008. Epub 2014 Apr 1.


Efficient detection of factor IX mutations by denaturing high-performance liquid chromatography in Taiwanese hemophilia B patients, and the identification of two novel mutations.

Lin PC, Su YN, Liao YM, Chang TT, Tsai SP, Shu HL, Chiou SS.

Kaohsiung J Med Sci. 2014 Apr;30(4):187-93. doi: 10.1016/j.kjms.2013.12.003. Epub 2014 Jan 6.


Concordant myelomeningocele in dizygotic twins conceived by intracytoplasmic sperm injection, in vitro fertilization, and embryo transfer.

Chen CP, Hwu YM, Chen CY, Su YN, Lin TH, Kuo YL, Chern SR, Wang W.

Taiwan J Obstet Gynecol. 2013 Dec;52(4):611-2. doi: 10.1016/j.tjog.2013.10.032. No abstract available.


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

Chen CP, Su YN, Lin TH, Chang TY, Su JW, Wang W.

Taiwan J Obstet Gynecol. 2013 Dec;52(4):580-5. doi: 10.1016/j.tjog.2013.10.023. Review.


A feasible strategy of preimplantation genetic diagnosis for carriers with chromosomal translocation: Using blastocyst biopsy and array comparative genomic hybridization.

Huang CC, Chang LJ, Tsai YY, Hung CC, Fang MY, Su YN, Chen HF, Chen SU.

J Formos Med Assoc. 2013 Sep;112(9):537-44. doi: 10.1016/j.jfma.2013.02.010. Epub 2013 Apr 8.


Perfluorinated compound levels in cord blood and neurodevelopment at 2 years of age.

Chen MH, Ha EH, Liao HF, Jeng SF, Su YN, Wen TW, Lien GW, Chen CY, Hsieh WS, Chen PC.

Epidemiology. 2013 Nov;24(6):800-8. doi: 10.1097/EDE.0b013e3182a6dd46.


Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review.

Chen CP, Su YN, Chen CY, Chern SR, Wu PS, Su JW, Lee CC, Chen LF, Wang W.

Genomics. 2013 Oct;102(4):265-9. doi: 10.1016/j.ygeno.2013.08.003. Epub 2013 Aug 24.


Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review.

Chen CP, Chen M, Su YN, Huang JP, Chern SR, Wu PS, Su JW, Chang SP, Chen YT, Lee CC, Chen LF, Pan CW, Wang W.

Gene. 2013 Oct 15;529(1):169-75. doi: 10.1016/j.gene.2013.07.048. Epub 2013 Aug 7. Review.


Rapid detection of de novo P253R mutation in FGFR2 using uncultured amniocytes in a pregnancy affected by polyhydramnios, Blake's pouch cyst, and Apert syndrome.

Chen CP, Su YN, Chang TY, Chern SR, Chen CY, Su JW, Wang W.

Taiwan J Obstet Gynecol. 2013 Jun;52(2):273-7. doi: 10.1016/j.tjog.2013.04.022.


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

Lin TH, Chung CH, Shih JC, Lin CH, Lee CN, Su YN.

Taiwan J Obstet Gynecol. 2013 Jun;52(2):267-9. doi: 10.1016/j.tjog.2013.04.020. Review.


Lethal fetal stroke in utero.

Lin TH, Lee CN, Su YN.

Taiwan J Obstet Gynecol. 2013 Jun;52(2):264-6. doi: 10.1016/j.tjog.2013.04.019.


Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13.

Su PH, Chen CP, Su YN, Chen SJ, Lin LL, Chen JY.

Genet Mol Res. 2013 Apr 25;12(2):1311-7. doi: 10.4238/2013.April.25.2.

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