Full text in PMC (nucleotide) for Gene (Select 55636) - PMC

Yousef Ashraf Tawfik Morcos, Gregoire Najjar, Sabine Meessen, Britta Witt, Anca Azoitei, Mukesh Kumar, Gamal Wakileh, Klaus Schwarz, Hubert Schrezenmeier, Friedemann Zengerling, Christian Bolenz, Cagatay Günes

Int J Mol Sci. 2020 Jan; 21(1): 85. Published online 2019 Dec 20. doi: 10.3390/ijms21010085

PMCID:: PMC6981981

Abstract Article PDF–6.4M

Select item 69489494.

Gli3 Regulates Vomeronasal Neurogenesis, Olfactory Ensheathing Cell Formation, and GnRH-1 Neuronal Migration

Ed Zandro M. Taroc, Ankana S. Naik, Jennifer M. Lin, Nicolas B. Peterson, David L. Keefe, Jr., Elizabet Genis, Gabriele Fuchs, Ravikumar Balasubramanian, Paolo E. Forni

J Neurosci. 2020 Jan 8; 40(2): 311–326. doi: 10.1523/JNEUROSCI.1977-19.2019

PMCID:: PMC6948949

Abstract Article PDF–11M

Select item 69003935.

Gene‐level genome‐wide association analysis of suicide attempt, a preliminary study in a psychiatric Mexican population

Thelma Beatriz González‐Castro, José Jaime Martínez‐Magaña, Carlos Alfonso Tovilla‐Zárate, Isela Esther Juárez‐Rojop, Emmanuel Sarmiento, Alma Delia Genis‐Mendoza, Humberto Nicolini

Mol Genet Genomic Med. 2019 Dec; 7(12): e983. Published online 2019 Oct 2. doi: 10.1002/mgg3.983

PMCID:: PMC6900393

Abstract Article PDF–604K

Select item 68171286.

Rare LPL gene missense mutation in an infant with hypertriglyceridemia

Yuan‐yuan Qin, Ai‐qiu Wei, Qing‐wen Shan, Xiao‐ying Xian, Yang‐yang Wu, Lin Liao, Jie Yan, Zhan‐feng Lai, Fa‐quan Lin

J Clin Lab Anal. 2018 Jul; 32(6): e22414. Published online 2018 Feb 25. doi: 10.1002/jcla.22414

PMCID:: PMC6817128

Abstract Article PDF–531K

Select item 67467707.

Metadherin enhances vulnerability of cancer cells to ferroptosis

Jianling Bi, Shujie Yang, Long Li, Qun Dai, Nicholas Borcherding, Brett A. Wagner, Garry R. Buettner, Douglas R. Spitz, Kimberly K. Leslie, Jun Zhang, Xiangbing Meng

Cell Death Dis. 2019 Oct; 10(10): 682. Published online 2019 Sep 17. doi: 10.1038/s41419-019-1897-2

PMCID:: PMC6746770

Abstract Article PDF–2.2M

Select item 67353628.

GPR124 facilitates pericyte polarization and migration by regulating the formation of filopodia during ischemic injury

Dan-Yang Chen, Ning-He Sun, Ya-Ping Lu, Ling-Juan Hong, Tian-Tian Cui, Cheng-Kun Wang, Xing-Hui Chen, Shuai-Shuai Wang, Li-Li Feng, Wei-Xing Shi, Kohji Fukunaga, Zhong Chen, Ying-Mei Lu, Feng Han

Theranostics. 2019; 9(20): 5937–5955. Published online 2019 Aug 14. doi: 10.7150/thno.34168

PMCID:: PMC6735362

Abstract Article PDF–16M

Select item 67273919.

A cross-sectional study on factors associated with hypertension and genetic polymorphisms of renin-angiotensin-aldosterone system in Chinese hui pilgrims to hajj

Yinxia Zhang, Fangfang Shi, Zhanbiao Yu, Aimin Yang, Maolan Zeng, Jiaoyue Wang, Haiping Yin, Benzhong Zhang, Xiao Ma

BMC Public Health. 2019; 19: 1223. Published online 2019 Sep 4. doi: 10.1186/s12889-019-7357-1

PMCID:: PMC6727391

Abstract Article PDF–1.7M

Select item 671226910.

肺癌组织中DNA聚合酶β基因突变的研究

吴青峻, 田文鑫, 于瀚博, 黄川, 焦鹏, 马超, 王永忠, 黄文, 孙耀光, 艾斌, 佟宏峰

Zhongguo Fei Ai Za Zhi. 2019 Jul 20; 22(7): 427–432. Chinese. doi: 10.3779/j.issn.1009-3419.2019.07.04

PMCID:: PMC6712269

Abstract Article PDF–2.0M

Select item 670815711.

Diversity of ATM gene variants: a population-based genome data analysis for precision medicine

Hisanori Fukunaga, Yasuyuki Taki, Kevin M. Prise

Hum Genomics. 2019; 13: 38. Published online 2019 Aug 23. doi: 10.1186/s40246-019-0234-2

PMCID:: PMC6708157

Abstract Article PDF–616K

Select item 670017912.

Comprehensive analysis of syndromic hearing loss patients in Japan

Michie Ideura, Shin-ya Nishio, Hideaki Moteki, Yutaka Takumi, Maiko Miyagawa, Teruyuki Sato, Yumiko Kobayashi, Kenji Ohyama, Kiyoshi Oda, Takamichi Matsui, Tsukasa Ito, Hiroshi Suzumura, Kyoko Nagai, Shuji Izumi, Nobuhiro Nishiyama, Manabu Komori, Kozo Kumakawa, Hidehiko Takeda, Yoko Kishimoto, Satoshi Iwasaki, Sakiko Furutate, Kotaro Ishikawa, Masato Fujioka, Hiroshi Nakanishi, Jun Nakayama, Rie Horie, Yumi Ohta, Yasushi Naito, Mariko Kakudo, Hirofumi Sakaguchi, Yuko Kataoka, Kazuma Sugahara, Naohito Hato, Takashi Nakagawa, Nana Tsuchihashi, Yukihiko Kanda, Chiharu Kihara, Tetsuya Tono, Ikuyo Miyanohara, Akira Ganaha, Shin-ichi Usami

Sci Rep. 2019; 9: 11976. Published online 2019 Aug 19. doi: 10.1038/s41598-019-47141-4

PMCID:: PMC6700179

Abstract Article PDF–1017K

Select item 663760613.

A novel CHD7 variant disrupting acceptor splice site in a patient with mild features of CHARGE syndrome: a case report

Evelina Siavrienė, Gunda Petraitytė, Violeta Mikštienė, Tautvydas Rančelis, Živilė Maldžienė, Aušra Morkūnienė, Jekaterina Byčkova, Algirdas Utkus, Vaidutis Kučinskas, Eglė Preikšaitienė

BMC Med Genet. 2019; 20: 127. Published online 2019 Jul 17. doi: 10.1186/s12881-019-0859-y

PMCID:: PMC6637606

Abstract Article PDF–775K

Select item 662503014.

TFAP2C increases cell proliferation by downregulating GADD45B and PMAIP1 in non-small cell lung cancer cells

Hyunhee Do, Dain Kim, JiHoon Kang, Beomseok Son, Danbi Seo, HyeSook Youn, BuHyun Youn, Wanyeon Kim

Biol Res. 2019; 52: 35. Published online 2019 Jul 11. doi: 10.1186/s40659-019-0244-5

PMCID:: PMC6625030

Abstract Article PDF–2.1M

Select item 659430315.

Functional Hypogonadotropic Hypogonadism in Men: Underlying Neuroendocrine Mechanisms and Natural History

Andrew A Dwyer, Niraj R Chavan, Hilana Lewkowitz-Shpuntoff, Lacey Plummer, Frances J Hayes, Stephanie B Seminara, William F Crowley, Jr., Nelly Pitteloud, Ravikumar Balasubramanian

J Clin Endocrinol Metab. 2019 Aug; 104(8): 3403–3414. Published online 2019 Mar 11. doi: 10.1210/jc.2018-02697

PMCID:: PMC6594303

Abstract Article

Select item 656554616.

Clinical utility in infants with suspected monogenic conditions through next‐generation sequencing

Sha Hong, Li Wang, Dongying Zhao, Yonghong Zhang, Yan Chen, Jintong Tan, Lili Liang, Tianwen Zhu

Mol Genet Genomic Med. 2019 Jun; 7(6): e684. Published online 2019 Apr 9. doi: 10.1002/mgg3.684

PMCID:: PMC6565546

Abstract Article PDF–931K

Select item 654368417.

Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants

Xiang Chen, Kai Yan, Yanyan Gao, Huijun Wang, Guoqiang Chen, Bingbing Wu, Qian Qin, Lin Yang, Wenhao Zhou

BMC Med Genet. 2019; 20: 93. Published online 2019 May 30. doi: 10.1186/s12881-019-0813-z

PMCID:: PMC6543684

Abstract Article PDF–863K

Select item 651755818.

Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients

Péter Balicza, Noémi Ágnes Varga, Bence Bolgár, Klára Pentelényi, Renáta Bencsik, Anikó Gál, András Gézsi, Csilla Prekop, Viktor Molnár, Mária Judit Molnár

Front Genet. 2019; 10: 434. Published online 2019 May 8. doi: 10.3389/fgene.2019.00434

PMCID:: PMC6517558

Abstract Article PDF–3.0M

Select item 646565719.

Integrated bioinformatics analysis of key genes involved in progress of colon cancer

Haojie Yang, Jiong Wu, Jingjing Zhang, Zhigang Yang, Wei Jin, Ying Li, Lei Jin, Lu Yin, Hua Liu, Zhenyi Wang

Mol Genet Genomic Med. 2019 Apr; 7(4): e00588. Published online 2019 Feb 11. doi: 10.1002/mgg3.588

PMCID:: PMC6465657

Abstract Article PDF–1017K

Select item 645279920.

Genetic polymorphisms in Sox17 associated with intracranial aneurysm in Chinese Han people: a genotype-phenotype study

Mengqi Li, Weihan Wang, Lin Zhang, Wenqiang Xin, Yan Zhao, Linchun Huan, Jianjun Yu, Hao Zhang, Jianning Zhang, Shuyuan Yang, Degang Liang, Weidong Yang, Xinyu Yang

Neuropsychiatr Dis Treat. 2019; 15: 779–783. Published online 2019 Apr 2. doi: 10.2147/NDT.S193478

Correction in:: Neuropsychiatr Dis Treat. 2019; 15: 2291.

PMCID:: PMC6452799

Abstract Article PDF–199K

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