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Select item 70380921.

High Mobility Group A (HMGA): Chromatin Nodes Controlled by a Knotty miRNA Network

Riccardo Sgarra, Silvia Pegoraro, Daniela D’Angelo, Gloria Ros, Rossella Zanin, Michela Sgubin, Sara Petrosino, Sabrina Battista, Guidalberto Manfioletti

Int J Mol Sci. 2020 Feb; 21(3): 717. Published online 2020 Jan 22. doi: 10.3390/ijms21030717

PMCID:: PMC7038092

Article PDF–2.5M

Select item 70271952.

Systematic Nucleotide Exchange Analysis of ESTs From the Human Cancer Genome Project Report: Origins of 347 Unknown ESTs Indicate Putative Transcription of Non-Coding Genomic Regions

Ganesh Warthi, Pierre-Edouard Fournier, Hervé Seligmann

Front Genet. 2020; 11: 42. Published online 2020 Feb 11. doi: 10.3389/fgene.2020.00042

PMCID:: PMC7027195

Article PDF–1.2M

Select item 70204503.

T-2 Toxin-Induced Oxidative Stress Leads to Imbalance of Mitochondrial Fission and Fusion to Activate Cellular Apoptosis in the Human Liver 7702 Cell Line

Junhua Yang, Wenbo Guo, Jianhua Wang, Xianli Yang, Zhiqi Zhang, Zhihui Zhao

Toxins (Basel) 2020 Jan; 12(1): 43. Published online 2020 Jan 10. doi: 10.3390/toxins12010043

PMCID:: PMC7020450

Article PDF–6.3M

Select item 70191354.

Clinical and Molecular Characterization and Discovery of Novel Genetic Mutations of Chinese Patients with COL2A1-related Dysplasia

Yang Xu, Li Li, Chun Wang, Hua Yue, Hao Zhang, Jiemei Gu, Weiwei Hu, Lianyong Liu, Zhenlin Zhang

Int J Biol Sci. 2020; 16(5): 859–868. Published online 2020 Jan 16. doi: 10.7150/ijbs.38811

PMCID:: PMC7019135

Article PDF–1.6M

Select item 70068645.

A Look at Genetic Linkage between Clozapine-induced Agranulocytosis, Malignant Hyperthermia, Neuroleptic Malignant Syndrome, and Statin-induced Myopathy

Nitin Pothen, Shveta Kansal, Theodor Rais, Stacy Doumas, Ramon Solhkhah

Innov Clin Neurosci. 2019 Nov 1; 16(11-12): 28–31. Published online Nov-Dec 2019.

PMCID:: PMC7006864

Article PDF–127K

Select item 69782296.

Candidate modifier genes for immune function in 22q11.2 deletion syndrome

Catherina T. Pinnaro, Travis Henry, Heather J. Major, Mrutyunjaya Parida, Lucy E. DesJardin, John R. Manak, Benjamin W. Darbro

Mol Genet Genomic Med. 2020 Jan; 8(1): e1057. Published online 2019 Dec 12. doi: 10.1002/mgg3.1057

PMCID:: PMC6978229

Article PDF–761K

Select item 68903727.

The expression and prognostic significance of Drp1 in lung cancer: A bioinformatics analysis and immunohistochemistry

Lingling Yu, Zuke Xiao, Hongying Tu, Bo Tong, Shengsong Chen

Medicine (Baltimore) 2019 Nov; 98(48): e18228. Published online 2019 Nov 27. doi: 10.1097/MD.0000000000018228

PMCID:: PMC6890372

Article PDF–1.6M

Select item 68569498.

Complete Multilineage CD4 Expression Defect Associated With Warts Due to an Inherited Homozygous CD4 Gene Mutation

Rosa Anita Fernandes, Martin Perez-Andres, Elena Blanco, Maria Jara-Acevedo, Ignacio Criado, Julia Almeida, Vitor Botafogo, Ines Coutinho, Artur Paiva, Jacques J. M. van Dongen, Alberto Orfao, Emilia Faria

Front Immunol. 2019; 10: 2502. Published online 2019 Nov 8. doi: 10.3389/fimmu.2019.02502

PMCID:: PMC6856949

Article PDF–1.7M

Select item 68528009.

IL-6 Impairs the Activity of Vitamin D₃ in the Regulation of Epithelial-Mesenchymal Transition in Triple Negative Breast Cancer

Mohamed A. Abdel-Mohsen, Samar. M Abo-Deif, Lobna A. Abou-Shamaa

Asian Pac J Cancer Prev. 2019; 20(8): 2267–2273. doi: 10.31557/APJCP.2019.20.8.2267

PMCID:: PMC6852800

Article PDF–780K

Select item 678543910.

De novo pathogenic DNM1L variant in a patient diagnosed with atypical hereditary sensory and autonomic neuropathy

Maja Tarailo‐Graovac, Farah R. Zahir, Irena Zivkovic, Michelle Moksa, Kathryn Selby, Sunita Sinha, Corey Nislow, Sylvia G. Stockler‐Ipsiroglu, Ruth Sheffer, Ann Saada‐Reisch, Jan M. Friedman, Clara D. M. van Karnebeek, Gabriella A. Horvath

Mol Genet Genomic Med. 2019 Oct; 7(10): e00961. Published online 2019 Sep 1. doi: 10.1002/mgg3.961

PMCID:: PMC6785439

Article PDF–366K

Select item 673909711.

Mitochondrial protein import is regulated by p17/PERMIT to mediate lipid metabolism and cellular stress

Natalia Oleinik, Jisun Kim, Braden M. Roth, Shanmugam Panneer Selvam, Monika Gooz, Roger H. Johnson, John J. Lemasters, Besim Ogretmen

Sci Adv. 2019 Sep; 5(9): eaax1978. Published online 2019 Sep 11. doi: 10.1126/sciadv.aax1978

PMCID:: PMC6739097

Article PDF–1.8M

Select item 670268712.

Different gene expression profiles in subcutaneous & visceral adipose tissues from Mexican patients with obesity

María D. Ronquillo, Alla Mellnyk, Noemí Cárdenas-Rodríguez, Emmanuel Martínez, David A. Comoto, Liliana Carmona-Aparicio, Norma E. Herrera, Eleazar Lara, Armando Pereyra, Esaú Floriano-Sánchez

Indian J Med Res. 2019 May; 149(5): 616–626. doi: 10.4103/ijmr.IJMR_1165_17

PMCID:: PMC6702687

Article PDF–1.3M

Select item 665926413.

Relationship between ALDH2 genotype and in-stent restenosis in Chinese Han patients after percutaneous coronary intervention

Lizhi Lv, Weijie Ye, Peiyuan Song, Yubin Chen, Jing Yang, Congmin Zhang, Xiaoping Chen, Fanyan Luo

BMC Cardiovasc Disord. 2019; 19: 176. Published online 2019 Jul 25. doi: 10.1186/s12872-019-1161-9

PMCID:: PMC6659264

Article PDF–1.3M

Select item 663550914.

Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy

Amitabh Biswas, Ali Raza, Soumi Das, Mitali Kapoor, Rijith Jayarajan, Ankit Verma, Karuthedath Vellarikkal Shamsudheen, Benrithung Murry, Sandeep Seth, Balram Bhargava, Vinod Scaria, Sridhar Sivasubbu, Vadlamudi Raghavendra Rao

Purinergic Signal. 2019 Jun; 15(2): 205–210. Published online 2019 May 31. doi: 10.1007/s11302-019-09660-7

PMCID:: PMC6635509

Article PDF–2.1M

Select item 656384715.

Evaluation of Methods for the Extraction of Microbial DNA From Vaginal Swabs Used for Microbiome Studies

Valentina Mattei, Selvasankar Murugesan, Muna Al Hashmi, Rebecca Mathew, Nicola James, Parul Singh, Manoj Kumar, Arun Prasath Lakshmanan, Annalisa Terranegra, Souhaila Al Khodor, Sara Tomei

Front Cell Infect Microbiol. 2019; 9: 197. Published online 2019 Jun 6. doi: 10.3389/fcimb.2019.00197

PMCID:: PMC6563847

Article PDF–1.4M

Select item 654955816.

De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures

Nurit Assia Batzir, Pranjali K. Bhagwat, Tanya N. Eble, Pengfei Liu, Christine M. Eng, Sarah H. Elsea, Laurie A. Robak, Fernando Scaglia, Alica M. Goldman, Shweta U. Dhar, Michael F. Wangler

Cold Spring Harb Mol Case Stud. 2019 Jun; 5(3): a003673. doi: 10.1101/mcs.a003673