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Direct imaging of dopant sites in rare-earth element-doped permanent magnet and correlated magnetism origin.

Xue Zeng, Junwei Zhang, Mingsu Si, Derang Cao, Xia Deng, Hongbin Ma, Qianqian Lan, Desheng Xue, Xixiang Zhang, Kun Tao, Yong Peng,

Identifying the dopants and their occupation sites in rare-earth-doped permanent magnets is critical not only to understand the mechanism of tuning their magnetic properties, but also to develop guiding principles to further improve their performance. In this study, we present a direct observation of the preferred atomic sites of La ... Read more >>

Nanoscale (Nanoscale)
[2019, 11(10):4385-4393]

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Circulating CD14+HLA-DR-/low Myeloid-Derived Suppressor Cells as Potential Biomarkers for the Identification of Psoriasis TCM Blood-Heat Syndrome and Blood-Stasis Syndrome.

Shipeng Sun, Yali Wei, Xue Zeng, Yuliang Yuan, Na Wang, Cheng An, Jinlong Duan, Bo Pang, Zifu Hong, Guijian Liu,

Psoriasis is a chronic autoimmune disease. Identification of the biomarkers responsible for Traditional Chinese Medicine (TCM) syndromes of psoriasis can help researchers recognize the different aspects of psoriasis and find novel therapeutic targets for the treatment of psoriasis. The current study investigated the levels of circulating Mo-MDSCs and Mo-MDSC-associated immune ... Read more >>

Evid Based Complement Alternat Med (Evidence-based complementary and alternative medicine : eCAM)
[2020, 2020:4582459]

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Interfacial Roughness Facilitated by Dislocation and a Metal-Fuse Resistor Fabricated Using a Nanomanipulator.

Junwei Zhang, Rongrong Chen, Xian Li, Yong Peng, Hongbin Ma, Yang Hu, Xue Zeng, Xia Deng, Chaoshuai Guan, Yue Hu, Mingjie Zhang, Abdul Karim, Kun Tao, Xixiang Zhang,

Granular magnetic systems consisting of magnetic nanoparticles embedded in a nonmagnetic metallic matrix have emerged as an attractive building block for nanodevices. A key challenge for building interface-based nanodevice applications, such as magnetic memory devices, is to clearly know about the influences of interfacial roughness on the scattering of conduction ... Read more >>

ACS Appl Mater Interfaces (ACS applied materials & interfaces)
[2020, 12(21):24442-24449]

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MicroRNA-125a-5p modulates radioresistance in LTEP-a2 non-small cell lung cancer cells by targeting SIRT7.

Chaonan Sun, Xue Zeng, Hong Guo, Tianlu Wang, Linlin Wei, Yaotian Zhang, Jiaming Zhao, Xinchi Ma, Na Zhang,

BACKGROUND:Micro(mi)RNAs are a series of 20-24 nt non-coding small-molecule single-stranded RNAs that are believed to be closely related to tumor occurrence, development and other biological processes. MicroRNA-125a modulates radiochemotherapy sensitivity. However, the mechanism by which miRNA-125a regulates radiation resistance by lung cancer cells is yet to be elucidated. OBJECTIVE:The present ... Read more >>

Cancer Biomark (Cancer biomarkers : section A of Disease markers)
[2020, 27(1):39-49]

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Novel OTOF pathogenic variant segregating with non-syndromic hearing loss in a consanguineous family from tribal Rajouri in Jammu and Kashmir.

Raja A H Kuchay, Yaser Rafiq Mir, Xue Zeng, Asima Hassan, Kazunori Namba, Mustafa Tekin,

BACKGROUND:Hereditary hearing loss is characterized by a very high genetic heterogeneity. The OTOF (Locus: DFNB9), encoding otoferlin, is reported to be one of the major causes of non-syndromic hearing loss, and is also reported to be the most common cause of non-syndromic recessive auditory neuropathy spectrum disorder. METHODS:In this study, ... Read more >>

Int. J. Pediatr. Otorhinolaryngol. (International journal of pediatric otorhinolaryngology)
[2020, 130:109831]

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Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3.

August A Allocco, Sheng Chih Jin, Phan Q Duy, Charuta G Furey, Xue Zeng, Weilai Dong, Carol Nelson-Williams, Jason K Karimy, Tyrone DeSpenza, Le T Hao, Benjamin Reeves, Shozeb Haider, Murat Gunel, Richard P Lifton, Kristopher T Kahle,

Background:ATP1A3 encodes the α3 subunit of the Na+/K+ ATPase, a fundamental ion-transporting enzyme. Primarily expressed in neurons, ATP1A3 is mutated in several autosomal dominant neurological diseases. To our knowledge, damaging recessive genotypes in ATP1A3 have never been associated with any human disease. Atp1a3 deficiency in zebrafish results in hydrocephalus; however, ... Read more >>

Front Cell Neurosci (Frontiers in cellular neuroscience)
[2019, 13:425]

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SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus.

Sheng Chih Jin, Charuta G Furey, Xue Zeng, August Allocco, Carol Nelson-Williams, Weilai Dong, Jason K Karimy, Kevin Wang, Shaojie Ma, Eric Delpire, Kristopher T Kahle,

BACKGROUND:Congenital hydrocephalus (CH) is a highly morbid disease that features enlarged brain ventricles and impaired cerebrospinal fluid homeostasis. Although early linkage or targeted sequencing studies in large multigenerational families have localized several genes for CH, the etiology of most CH cases remains unclear. Recent advances in whole exome sequencing (WES) ... Read more >>

Mol Genet Genomic Med (Molecular genetics & genomic medicine)
[2019, 7(9):e892]

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LncRNA LINC00963 Promotes Tumorigenesis and Radioresistance in Breast Cancer by Sponging miR-324-3p and Inducing ACK1 Expression.

Na Zhang, Xue Zeng, Chaonan Sun, Hong Guo, Tianlu Wang, Linlin Wei, Yaotian Zhang, Jiaming Zhao, Xinchi Ma,

Upregulation of long non-coding RNA LINC00963 has been observed in several cancer types. In this study, we analyzed the clinical and biological significance of LINC00963 in breast cancer. The key microRNA (miR) mediating the action of LINC00963 was identified. We show that LINC00963 upregulation is correlated with aggressive parameters of ... Read more >>

Mol Ther Nucleic Acids (Molecular therapy. Nucleic acids)
[2019, 18:871-881]

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FEN1 mediates miR-200a methylation and promotes breast cancer cell growth via MET and EGFR signaling.

Xue Zeng, Xiujuan Qu, Chenyang Zhao, Lu Xu, Kezuo Hou, Yunpeng Liu, Na Zhang, Jing Feng, Sha Shi, Lingyun Zhang, Jiawen Xiao, Zhigang Guo, Yuee Teng, Xiaofang Che,

Flap endonuclease 1 (FEN1) is recognized as a pivotal factor in DNA replication, long-patch excision repair, and telomere maintenance. Excessive FEN1 expression has been reported to be closely associated with cancer progression, but the specific mechanism has not yet been explored. In the present study, we demonstrated that FEN1 promoted ... Read more >>

FASEB J. (FASEB journal : official publication of the Federation of American Societies for Experimental Biology)
[2019, 33(10):10717-10730]

Cited: 1 time

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ARSACS as a Worldwide Disease: Novel SACS Mutations Identified in a Consanguineous Family from the Remote Tribal Jammu and Kashmir Region in India.

Raja A H Kuchay, Yaser Rafiq Mir, Xue Zeng, Asima Hassan, Javed Musarrat, Iqbal Parwez, Christoph Kernstock, Andreas Traschütz, Matthis Synofzik,

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a rare neurodegenerative disorder characterized by the triad of early-onset cerebellar ataxia, peripheral sensorimotor neuropathy, and lower limb spasticity. Here, we present a 28-year-old male patient with symptoms of ARSACS and mild intellectual disability from a consanguineous family of tribal J&K, India. ... Read more >>

Cerebellum (Cerebellum (London, England))
[2019, 18(4):807-812]

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De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.

Katherine L Helbig, Robert J Lauerer, Jacqueline C Bahr, Ivana A Souza, Candace T Myers, Betül Uysal, Niklas Schwarz, Maria A Gandini, Sun Huang, Boris Keren, Cyril Mignot, Alexandra Afenjar, Thierry Billette de Villemeur, Delphine Héron, Caroline Nava, Stéphanie Valence, Julien Buratti, Christina R Fagerberg, Kristina P Soerensen, Maria Kibaek, Erik-Jan Kamsteeg, David A Koolen, Boudewijn Gunning, H Jurgen Schelhaas, Michael C Kruer, Jordana Fox, Somayeh Bakhtiari, Randa Jarrar, Sergio Padilla-Lopez, Kristin Lindstrom, Sheng Chih Jin, Xue Zeng, Kaya Bilguvar, Antigone Papavasileiou, Qinghe Xing, Changlian Zhu, Katja Boysen, Filippo Vairo, Brendan C Lanpher, Eric W Klee, Jan-Mendelt Tillema, Eric T Payne, Margot A Cousin, Teresa M Kruisselbrink, Myra J Wick, Joshua Baker, Eric Haan, Nicholas Smith, Azita Sadeghpour, Erica E Davis, Nicholas Katsanis, , Mark A Corbett, Alastair H MacLennan, Jozef Gecz, Saskia Biskup, Eva Goldmann, Lance H Rodan, Elizabeth Kichula, Eric Segal, Kelly E Jackson, Alexander Asamoah, David Dimmock, Julie McCarrier, Lorenzo D Botto, Francis Filloux, Tatiana Tvrdik, Gregory D Cascino, Sherry Klingerman, Catherine Neumann, Raymond Wang, Jessie C Jacobsen, Melinda A Nolan, Russell G Snell, Klaus Lehnert, Lynette G Sadleir, Britt-Marie Anderlid, Malin Kvarnung, Renzo Guerrini, Michael J Friez, Michael J Lyons, Jennifer Leonhard, Gabriel Kringlen, Kari Casas, Christelle M El Achkar, Lacey A Smith, Alexander Rotenberg, Annapurna Poduri, Alba Sanchis-Juan, Keren J Carss, Julia Rankin, Adam Zeman, F Lucy Raymond, Moira Blyth, Bronwyn Kerr, Karla Ruiz, Jill Urquhart, Imelda Hughes, Siddharth Banka, , Ulrike B S Hedrich, Ingrid E Scheffer, Ingo Helbig, Gerald W Zamponi, Holger Lerche, Heather C Mefford,

Am. J. Hum. Genet. (American journal of human genetics)
[2019, 104(3):562]

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EphrinB2-EphB4-RASA1 Signaling in Human Cerebrovascular Development and Disease.

Xue Zeng, Ava Hunt, Sheng Chih Jin, Daniel Duran, Jonathan Gaillard, Kristopher T Kahle,

Recent whole exome sequencing studies in humans have provided novel insight into the importance of the ephrinB2-EphB4-RASA1 signaling axis in cerebrovascular development, corroborating and extending previous work in model systems. Here, we aim to review the human cerebrovascular phenotypes associated with ephrinB2-EphB4-RASA1 mutations, including those recently discovered in Vein of ... Read more >>

Trends Mol Med (Trends in molecular medicine)
[2019, 25(4):265-286]

Cited: 1 time

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Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation.

Daniel Duran, Xue Zeng, Sheng Chih Jin, Jungmin Choi, Carol Nelson-Williams, Bogdan Yatsula, Jonathan Gaillard, Charuta Gavankar Furey, Qiongshi Lu, Andrew T Timberlake, Weilai Dong, Michelle A Sorscher, Erin Loring, Jennifer Klein, August Allocco, Ava Hunt, Sierra Conine, Jason K Karimy, Mark W Youngblood, Jinwei Zhang, Michael L DiLuna, Charles C Matouk, Shrikant Mane, Irina R Tikhonova, Christopher Castaldi, Francesc López-Giráldez, James Knight, Shozeb Haider, Mariya Soban, Seth L Alper, Masaki Komiyama, Andrew F Ducruet, Joseph M Zabramski, Alan Dardik, Brian P Walcott, Christopher J Stapleton, Beverly Aagaard-Kienitz, Georges Rodesch, Eric Jackson, Edward R Smith, Darren B Orbach, Alejandro Berenstein, Kaya Bilguvar, Miikka Vikkula, Murat Gunel, Richard P Lifton, Kristopher T Kahle,

Normal vascular development includes the formation and specification of arteries, veins, and intervening capillaries. Vein of Galen malformations (VOGMs) are among the most common and severe neonatal brain arterio-venous malformations, shunting arterial blood into the brain's deep venous system through aberrant direct connections. Exome sequencing of 55 VOGM probands, including 52 ... Read more >>

Neuron (Neuron)
[2019, 101(3):429-443.e4]

Cited: 1 time

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Association of Glutathione s-transferase M1 and T1 gene polymorphisms with the susceptibility to acquired sensorineural hearing loss: a systematic review and meta-analysis.

Shimin Zong, Xue Zeng, Yexiao Guan, Tianyi Liu, Pan Luo, Fangmin Wan, Yanji Qu, Pei Chen, Hongjun Xiao,

Acquired sensorineural hearing loss (SNHL), including age-related hearing loss (ARHL), noise-induced hearing loss (NIHL), drug-induced hearing loss (DIHL) and sudden sensorineural hearing loss (SSHL), is one of the most common sensory deficits in humans. Several studies have reported that antioxidant gene glutathione s-transferase M1 and T1 (GST M1 and T1) ... Read more >>

Sci Rep (Scientific reports)
[2019, 9(1):833]

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Risk Factors and Pregnancy Outcomes: Complete versus Incomplete Placenta Previa in Mid-pregnancy.

Yun Feng, Xue-Yin Li, Juan Xiao, Wei Li, Jing Liu, Xue Zeng, Xi Chen, Kai-Yue Chen, Lei Fan, Qing-Ling Kang, Su-Hua Chen,

This prospective study was conducted to compare risk factors and pregnancy outcomes between women with complete placenta previa and those with incomplete placenta previa diagnosed in mid-pregnancy. The study was carried out from April 2014 to December 2015, during which 70 patients with complete previa and 113 with incomplete previa ... Read more >>

Curr Med Sci (Current medical science)
[2018, 38(4):597-601]

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Human Genetics and Molecular Mechanisms of Congenital Hydrocephalus.

Charuta Gavankar Furey, Xue Zeng, Weilai Dong, Sheng Chih Jin, Jungmin Choi, Andrew T Timberlake, Ashley M Dunbar, August A Allocco, Murat Günel, Richard P Lifton, Kristopher T Kahle,

World Neurosurg (World neurosurgery)
[2018, 119:441-443]

Cited: 1 time

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De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.

Katherine L Helbig, Robert J Lauerer, Jacqueline C Bahr, Ivana A Souza, Candace T Myers, Betül Uysal, Niklas Schwarz, Maria A Gandini, Sun Huang, Boris Keren, Cyril Mignot, Alexandra Afenjar, Thierry Billette de Villemeur, Delphine Héron, Caroline Nava, Stéphanie Valence, Julien Buratti, Christina R Fagerberg, Kristina P Soerensen, Maria Kibaek, Erik-Jan Kamsteeg, David A Koolen, Boudewijn Gunning, H Jurgen Schelhaas, Michael C Kruer, Jordana Fox, Somayeh Bakhtiari, Randa Jarrar, Sergio Padilla-Lopez, Kristin Lindstrom, Sheng Chih Jin, Xue Zeng, Kaya Bilguvar, Antigone Papavasileiou, Qinghe Xing, Changlian Zhu, Katja Boysen, Filippo Vairo, Brendan C Lanpher, Eric W Klee, Jan-Mendelt Tillema, Eric T Payne, Margot A Cousin, Teresa M Kruisselbrink, Myra J Wick, Joshua Baker, Eric Haan, Nicholas Smith, Azita Sadeghpour, Erica E Davis, Nicholas Katsanis, , Mark A Corbett, Alastair H MacLennan, Jozef Gecz, Saskia Biskup, Eva Goldmann, Lance H Rodan, Elizabeth Kichula, Eric Segal, Kelly E Jackson, Alexander Asamoah, David Dimmock, Julie McCarrier, Lorenzo D Botto, Francis Filloux, Tatiana Tvrdik, Gregory D Cascino, Sherry Klingerman, Catherine Neumann, Raymond Wang, Jessie C Jacobsen, Melinda A Nolan, Russell G Snell, Klaus Lehnert, Lynette G Sadleir, Britt-Marie Anderlid, Malin Kvarnung, Renzo Guerrini, Michael J Friez, Michael J Lyons, Jennifer Leonhard, Gabriel Kringlen, Kari Casas, Christelle M El Achkar, Lacey A Smith, Alexander Rotenberg, Annapurna Poduri, Alba Sanchis-Juan, Keren J Carss, Julia Rankin, Adam Zeman, F Lucy Raymond, Moira Blyth, Bronwyn Kerr, Karla Ruiz, Jill Urquhart, Imelda Hughes, Siddharth Banka, , Ulrike B S Hedrich, Ingrid E Scheffer, Ingo Helbig, Gerald W Zamponi, Holger Lerche, Heather C Mefford,

Developmental and epileptic encephalopathies (DEEs) are severe neurodevelopmental disorders often beginning in infancy or early childhood that are characterized by intractable seizures, abundant epileptiform activity on EEG, and developmental impairment or regression. CACNA1E is highly expressed in the central nervous system and encodes the α1-subunit of the voltage-gated CaV2.3 channel, ... Read more >>

Am. J. Hum. Genet. (American journal of human genetics)
[2018, 103(5):666-678]

Cited: 5 times

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De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.

Charuta Gavankar Furey, Jungmin Choi, Sheng Chih Jin, Xue Zeng, Andrew T Timberlake, Carol Nelson-Williams, M Shahid Mansuri, Qiongshi Lu, Daniel Duran, Shreyas Panchagnula, August Allocco, Jason K Karimy, Arjun Khanna, Jonathan R Gaillard, Tyrone DeSpenza, Prince Antwi, Erin Loring, William E Butler, Edward R Smith, Benjamin C Warf, Jennifer M Strahle, David D Limbrick, Phillip B Storm, Gregory Heuer, Eric M Jackson, Bermans J Iskandar, James M Johnston, Irina Tikhonova, Christopher Castaldi, Francesc López-Giráldez, Robert D Bjornson, James R Knight, Kaya Bilguvar, Shrikant Mane, Seth L Alper, Shozeb Haider, Bulent Guclu, Yasar Bayri, Yener Sahin, Michael L J Apuzzo, Charles C Duncan, Michael L DiLuna, Murat Günel, Richard P Lifton, Kristopher T Kahle,

Congenital hydrocephalus (CH), featuring markedly enlarged brain ventricles, is thought to arise from failed cerebrospinal fluid (CSF) homeostasis and is treated with lifelong surgical CSF shunting with substantial morbidity. CH pathogenesis is poorly understood. Exome sequencing of 125 CH trios and 52 additional probands identified three genes with significant burden of ... Read more >>

Neuron (Neuron)
[2018, 99(2):302-314.e4]

Cited: 9 times

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C-Cbl reverses HER2-mediated tamoxifen resistance in human breast cancer cells.

Wei Li, Ling Xu, Xiaofang Che, Haizhou Li, Ye Zhang, Na Song, Ti Wen, Kezuo Hou, Yi Yang, Lu Zhou, Xing Xin, Lu Xu, Xue Zeng, Sha Shi, Yunpeng Liu, Xiujuan Qu, Yuee Teng,

BACKGROUND:Tamoxifen is a frontline therapy for estrogen receptor (ER)-positive breast cancer in premenopausal women. However, many patients develop resistance to tamoxifen, and the mechanism underlying tamoxifen resistance is not well understood. Here we examined whether ER-c-Src-HER2 complex formation is involved in tamoxifen resistance. METHODS:MTT and colony formation assays were used ... Read more >>

BMC Cancer (BMC cancer)
[2018, 18(1):507]

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Early TCR Signaling Induces Rapid Aerobic Glycolysis Enabling Distinct Acute T Cell Effector Functions.

Ashley V Menk, Nicole E Scharping, Rebecca S Moreci, Xue Zeng, Cliff Guy, Sonia Salvatore, Heekyong Bae, Jianxin Xie, Howard A Young, Stacy Gelhaus Wendell, Greg M Delgoffe,

To fulfill bioenergetic demands of activation, T cells perform aerobic glycolysis, a process common to highly proliferative cells in which glucose is fermented into lactate rather than oxidized in mitochondria. However, the signaling events that initiate aerobic glycolysis in T cells remain unclear. We show T cell activation rapidly induces glycolysis independent of transcription, ... Read more >>

Cell Rep (Cell reports)
[2018, 22(6):1509-1521]

Cited: 26 times

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Cutaneous Metastases Arising from Synovial Sarcoma: A Case Report.

Xue Zeng, Li Li, Wa-Li Liu,

Chin. Med. J. (Chinese medical journal)
[2017, 130(24):3019-3020]

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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.

Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah Morton, Steven R DePalma, Xue Zeng, Hongjian Qi, Weni Chang, Michael C Sierant, Wei-Chien Hung, Shozeb Haider, Junhui Zhang, James Knight, Robert D Bjornson, Christopher Castaldi, Irina R Tikhonoa, Kaya Bilguvar, Shrikant M Mane, Stephan J Sanders, Seema Mital, Mark W Russell, J William Gaynor, John Deanfield, Alessandro Giardini, George A Porter, Deepak Srivastava, Cecelia W Lo, Yufeng Shen, W Scott Watkins, Mark Yandell, H Joseph Yost, Martin Tristani-Firouzi, Jane W Newburger, Amy E Roberts, Richard Kim, Hongyu Zhao, Jonathan R Kaltman, Elizabeth Goldmuntz, Wendy K Chung, Jonathan G Seidman, Bruce D Gelb, Christine E Seidman, Richard P Lifton, Martina Brueckner,

Congenital heart disease (CHD) is the leading cause of mortality from birth defects. Here, exome sequencing of a single cohort of 2,871 CHD probands, including 2,645 parent-offspring trios, implicated rare inherited mutations in 1.8%, including a recessive founder mutation in GDF1 accounting for ∼5% of severe CHD in Ashkenazim, recessive ... Read more >>

Nat. Genet. (Nature genetics)
[2017, 49(11):1593-1601]

Cited: 75 times

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FEN1 knockdown improves trastuzumab sensitivity in human epidermal growth factor 2-positive breast cancer cells.

Xue Zeng, Xiaofang Che, Yun-Peng Liu, Xiu-Juan Qu, Lu Xu, Chen-Yang Zhao, Chun-Lei Zheng, Ke-Zuo Hou, Yuee Teng,

Trastuzumab has been widely applied as a treatment for human epidermal growth factor 2 (HER2)-overexpressing breast cancer. However, the therapeutic efficacy of trastuzumab is limited. Flap endonuclease 1 (FEN1) is a multifunctional endonuclease that has a crucial role in DNA recombination and repair. Inhibition of FEN1 is associated with the ... Read more >>

Exp Ther Med (Experimental and therapeutic medicine)
[2017, 14(4):3265-3272]

Cited: 0 times

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Association of polymorphisms in heat shock protein 70 genes with the susceptibility to noise-induced hearing loss: A meta-analysis.

Shimin Zong, Xue Zeng, Tianyi Liu, Fangmin Wan, Pan Luo, Hongjun Xiao,

Several case-control studies reported the relationship between single nucleotide polymorphisms (SNPs) in HSP70 genes and noise-induced hearing loss (NIHL). However, their conclusions are conflicting. This meta-analysis aims to identify the association of HSP70 variants and NIHL susceptibility.A systematical literature search was performed in PubMed, Web of Science, EMBASE, and Wanfang ... Read more >>

PLoS ONE (PloS one)
[2017, 12(11):e0188195]

Cited: 2 times

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The value of transvaginal ultrasound in clinical surgical treatment of cesarean scar pregnancy.

Zhen Zeng, Shu-Ping Ding, Xue Zeng, Sui Cao, Ling-Yu Wei, Yan-Yan Liu, Fu-Yan Yang, Jing-Ji Gong, Han-Ping Chen, Xiao-Yan Xu,

The clinical value of transvaginal ultrasound in clinical surgical treatment of cesarean scar pregnancy (CSP) was evaluated. The clinical data of 104 patients with CSP admitted at Tongji Hospital from 2013 to 2016 were collected and analyzed retrospectively, including the patients' age, gestational age, the size of gestational sac or ... Read more >>

J. Huazhong Univ. Sci. Technol. Med. Sci. (Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban)
[2017, 37(4):536-540]

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