Torthaí cuardaigh - Bai‐Lin Wu
- 1 - 20 toradh as 32 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Cardiac regeneration: Unraveling the complex network of intercellular crosstalk de réir Bai‐Lin Wu, Florian Constanty, Arica Beisaw
Foilsithe / Cruthaithe 2025Revisão -
2
High Intensity ras Signaling Induces Premature Senescence by Activating p38 Pathway in Primary Human Fibroblasts de réir Qingdong Deng, Rong Liao, Bai‐Lin Wu, Peiqing Sun
Foilsithe / Cruthaithe 2004Artigo -
3
Mutations in <i>HFM1</i> in Recessive Primary Ovarian Insufficiency de réir Jian Wang, Wenxiang Zhang, Hong Jiang, Bai‐Lin Wu
Foilsithe / Cruthaithe 2014Carta -
4
<i>VANGL2</i>Mutations in Human Cranial Neural-Tube Defects de réir Yunping Lei, Ting Zhang, Hong Li, Bai Lin Wu, Jin Li, Hong Yan Wang
Foilsithe / Cruthaithe 2010Carta -
5
Autistic Children Exhibit Decreased Levels of Essential Fatty Acids in Red Blood Cells de réir Sarah Brigandi, Hong Shao, Steven Y. Qian, Yiping Shen, Bai‐Lin Wu, Jing X. Kang
Foilsithe / Cruthaithe 2015Artigo -
6
Genome-wide detection of natural selection in African Americans pre- and post-admixture de réir Wenfei Jin, Shuhua Xu, Haifeng Wang, Yongguo Yu, Yiping Shen, Bai-Lin Wu, Jin Li
Foilsithe / Cruthaithe 2011Artigo -
7
Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects de réir Gerald F. Cox, Joachim Bürger, Va Lip, Ulrike Mau, Karl Sperling, Bai‐Lin Wu, Bernhard Horsthemke
Foilsithe / Cruthaithe 2002Artigo -
8
Single-cell transcriptomic landscapes of the otic neuronal lineage at multiple early embryonic ages de réir Yuwei Sun, Luyue Wang, Tong Zhu, Bai‐Lin Wu, Guangqin Wang, Zhengnan Luo, Chao Li, Wu Wei, Zhiyong Liu
Foilsithe / Cruthaithe 2022Artigo -
9
Audiologic Phenotype and Progression in GJB2 (Connexin 26) Hearing Loss de réir Margaret A. Kenna, Henry A. Feldman, Marilyn W Neault, Anna Frangulov, Bai-Lin Wu, Brian J. Fligor, Heidi L. Rehm
Foilsithe / Cruthaithe 2010Artigo -
10
Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis de réir Irene Mademont‐Soler, Carmen Morales, Anna Soler, J. M. Martínez‐Crespo, Yinchen Shen, Ester Margarit, Núria Clusellas, María Obón, Bai‐Lin Wu, Aurora Sánchez
Foilsithe / Cruthaithe 2012Artigo -
11
Global DNA hypomethylation is associated with NTD‐affected pregnancy: A case‐control study de réir Xiaoli Chen, Jin Guo, Yunping Lei, Jizhen Zou, Xiaolin Lü, Yihua Bao, Lihua Wu, Jianxin Wu, Xiaoying Zheng, Yiping Shen, Bai‐Lin Wu, Ting Zhang
Foilsithe / Cruthaithe 2010Artigo -
12
A Genome-Wide Search for Signals of High-Altitude Adaptation in Tibetans de réir Shuhua Xu, S. Li, H. J. Yang, Jianxin Tan, Hua Jane Lou, Wenfei Jin, Li Yang, Xinwei Pan, Jian Wang, Yan Shen, Bai‐Lin Wu, Hongguang Wang, Jin Li
Foilsithe / Cruthaithe 2010Artigo -
13
Border-zone cardiomyocytes and macrophages regulate extracellular matrix remodeling to promote cardiomyocyte protrusion during cardiac regeneration de réir Florian Constanty, Bai‐Lin Wu, Ke-Hsuan Wei, I-Ting Lin, Julia Dallmann, Stefan Günther, Till Lautenschlaeger, Rashmi Priya, Shih-Lei Lai, Didier Y. R. Stainier, Arica Beisaw
Foilsithe / Cruthaithe 2025Artigo -
14
Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and spine growth and interfere with postnatal cortical development de réir Thị Kim Tuyền Đặng, Wenfeng Duan, Bin Yu, Dali Tong, Connie Cheng, Y F Zhang, Weiwei Wu, K Ye, W X Zhang, Meng Wu, Bai-Lin Wu, Yu An, Zilong Qiu, Bo Wu
Foilsithe / Cruthaithe 2017Artigo -
15
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss de réir Pu Dai, Qi Li, Deliang Huang, Yongyi Yuan, Dongyang Kang, David T. Miller, Hong Shao, Qingwen Zhu, Jia He, Fei Yu, Xin Liu, Bing Han, Huijun Yuan, Orah S. Platt, Dongyi Han, Bai-Lin Wu
Foilsithe / Cruthaithe 2008Artigo -
16
Genome-Wide Oligonucleotide Array Comparative Genomic Hybridization for Etiological Diagnosis of Mental Retardation de réir Bixia Xiang, Hongbo Zhu, Yiping Shen, David T. Miller, Kangmo Lu, Xiao Hu, Hans C. Andersson, Tarachandra M. Narumanchi, Yueying Wang, José E. Martínez, Bai-Lin Wu, Peining Li, Marilyn M. Li, Tian-Jian Chen, Yao‐Shan Fan
Foilsithe / Cruthaithe 2010Artigo -
17
Genome-wide Association of Copy-Number Variation Reveals an Association between Short Stature and the Presence of Low-Frequency Genomic Deletions de réir Andrew Dauber, Yongguo Yu, Michael C. Turchin, Charleston W. K. Chiang, Yan Meng, Ellen W. Demerath, Sanjay R. Patel, Stephen S. Rich, Jerome I. Rotter, Pamela J. Schreiner, James Wilson, Yiping Shen, Bai-Lin Wu, Joel N. Hirschhorn
Foilsithe / Cruthaithe 2011Artigo -
18
Homozygous <i>PLCB1</i> deletion associated with malignant migrating partial seizures in infancy de réir Annapurna Poduri, Sameer S. Chopra, Edward Neilan, Princess C. Elhosary, Manju A. Kurian, Esther Meyer, Brenda J. Barry, Omar Khwaja, Mustafa A. Salih, Tommy Stödberg, Ingrid E. Scheffer, Eamonn R. Maher, Mustafa Şahin, Bai‐Lin Wu, Gerard T. Berry, Christopher A. Walsh, Jonathan Picker, Sanjeev V. Kothare
Foilsithe / Cruthaithe 2012Artigo -
19
Genomic Dissection of Population Substructure of Han Chinese and Its Implication in Association Studies de réir Shuhua Xu, Xianyong Yin, Shilin Li, Wenfei Jin, Haiyi Lou, Ling Yang, Xiaohong Gong, Hongyan Wang, Yiping Shen, Xuedong Pan, Yungang He, Yajun Yang, Yi Wang, Wenqing Fu, Yu An, Jiucun Wang, Jingze Tan, Ji Qian, Xiaoli Chen, Xin Zhang, Yangfei Sun, Xuejun Zhang, Bai-Lin Wu, Jin Li
Foilsithe / Cruthaithe 2009Artigo -
20
Association between Microdeletion and Microduplication at 16p11.2 and Autism de réir Lauren A. Weiss, Yiping Shen, Joshua M. Korn, Dan E. Arking, David T. Miller, Ragnheiður Fossdal, Evald Sæmundsen, Hreinn Stefánsson, Todd Green, Orah S. Platt, Douglas M. Ruderfer, Christopher A. Walsh, David Altshuler, Aravinda Chakravarti, Rudolph E. Tanzi, Hreinn Stefánsson, Susan L. Santangelo, James F. Gusella, Pamela Sklar, Bai-Lin Wu, Mark J. Daly
Foilsithe / Cruthaithe 2008Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Medicine
Internal medicine
Psychiatry
Genome
Mutation
Phenotype
Psychology
Autism
Copy-number variation
Genotype
Neuroscience
Allele
Autism spectrum disorder
Population
Single-nucleotide polymorphism
Cell biology
Endocrinology
Evolutionary biology
Gene expression
Pregnancy
Allele frequency
Audiology
Chemistry
Chromosome
Cohort
Embryo
Environmental health