खोज परिणाम - "phenotyping"

TP63 mutation mapping information in TP63 mutation-associated syndromes द्वारा Yosuke Harazono, Kei-ichi Morita, Erina Tonouchi, Eri Anzai, Namiaki Takahara, Tomohiro Kohmoto, Issei Imoto, Tetsuya Yoda

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الارتباط وتحليل معامل المسار في حنطة الخبز

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Stem Cells as In Vitro Model of Parkinson's Disease द्वारा Patricia L. Martínez-Morales, Isabel Liste

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An Early Case of Complete Androgen Insensitivity Syndrome द्वारा Leen Matalka MD, S. Joy Dean MD, Giovanna Beauchamp MD, Bhuvana Sunil MD

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Clinical and molecular review of atypical congenital adrenal hyperplasia द्वारा Taninee Sahakitrungruang

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A network paradigm predicts drug synergistic effects using downstream protein-protein interactions द्वारा Jennifer L. Wilson, Ethan Steinberg, Rebecca Racz, Russ B. Altman, Nigam Shah, Kevin Grimes

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Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report द्वारा Ting Zeng, Linyan Liao, Yi Guo, Xuxu Liu, Xiaobo Xiong, Yu Zhang, Shi Cen, Honghui Li, Shuzhang Wei

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Clinical Findings in Children with Noonan Syndrome-A 17-Year Retrospective Study in an Oral Surgery Center द्वारा Anna Janas-Naze, Konrad Malkiewicz, Wei Zhang

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Current Progress in the Rejuvenation of Aging Stem/Progenitor Cells for Improving the Therapeutic Effectiveness of Myocardial Repair द्वारा Gurleen Kaur, Chuanxi Cai

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Factors impacting the height of the interproximal papilla: A cross‐sectional study द्वारा Hamdane Khaireddine, Tlili Mohamed, Rmida Arij, Khanfir Faten, Ben Amor Faten

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Clinical manifestations in a Chinese girl with heterozygous de novo NAA10 variant c. 247C > T, p. (Arg83Cys): a case report द्वारा Kaiyan Wei, Chaochun Zou

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Detection of genes involved in biofilm formation in Staphylococcus aureus isolates द्वारा Nourbakhsh, Fahimeh, Namvar, Amirmorteza Ebrahimzadeh

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Atypical deletion of Williams-Beuren syndrome reveals the mechanism of neurodevelopmental disorders द्वारा Jianrong Zhou, Ying Zheng, Guiying Liang, Xiaoli Xu, Jian Liu, Shaoxian Chen, Tongkai Ge, Pengju Wen, Yong Zhang, Xiaoqing Liu, Jian Zhuang, Yueheng Wu, Jimei Chen

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Arylamine N-acetyltransferase 2 genotype-dependent N-acetylation of isoniazid in cryopreserved human hepatocytes द्वारा Mark A. Doll, Raúl A. Salazar-González, Srineil Bodduluri, David W. Hein

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Modifications of Human Subcutaneous ADMSC after PPARγ Activation and Cold Exposition द्वारा Diana Vargas, Wendy Rosales, Fernando Lizcano

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Overview of Cardiomyopathies in Childhood द्वारा Anika Rath, Robert Weintraub, Robert Weintraub, Robert Weintraub

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Theaflavin-3,3'-Digallate from Black Tea Inhibits Neointima Formation Through Suppression of the PDGFRβ Pathway in Vascular Smooth Muscle Cells द्वारा Yichen Wu, Yichen Wu, Min Chen, Min Chen, Min Chen, Zilong Chen, Zilong Chen, Jiangcheng Shu, Jiangcheng Shu, Luoying Zhang, Jiong Hu, Hongjun Yu, Kai Huang, Kai Huang, Kai Huang, Kai Huang, Minglu Liang, Minglu Liang, Minglu Liang

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Case Report: A de novo CTNNB1 Nonsense Mutation Associated With Neurodevelopmental Disorder, Retinal Detachment, Polydactyly द्वारा Zhongling KE, Yanhui CHEN

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Manipulating Macrophage/Microglia Polarization to Treat Glioblastoma or Multiple Sclerosis द्वारा Thomas Kuntzel, Dominique Bagnard

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The Genetic and Molecular Basis of Developmental Language Disorder: A Review द्वारा Hayley S. Mountford, Ruth Braden, Dianne F. Newbury, Angela T. Morgan

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