Full text in PMC (nucleotide) for Gene (Select 3460) - PMC

Xi Luo, Simone Feurstein, Shruthi Mohan, Christopher C. Porter, Sarah A. Jackson, Sioban Keel, Michael Chicka, Anna L. Brown, Chimene Kesserwan, Anupriya Agarwal, Minjie Luo, Zejuan Li, Justyne E. Ross, Panagiotis Baliakas, Daniel Pineda-Alvarez, Courtney D. DiNardo, Alison A. Bertuch, Nikita Mehta, Tom Vulliamy, Ying Wang, Kim E. Nichols, Luca Malcovati, Michael F. Walsh, Lesley H. Rawlings, Shannon K. McWeeney, Jean Soulier, Anna Raimbault, Mark J. Routbort, Liying Zhang, Gabriella Ryan, Nancy A. Speck, Sharon E. Plon, David Wu, Lucy A. Godley

Blood Adv. 2019 Oct 22; 3(20): 2962–2979. Published online 2019 Oct 16. doi: 10.1182/bloodadvances.2019000644

PMCID:: PMC6849945

Abstract Article PDF–1.0M

Select item 65030134.

Genetic analysis of pharmacogenomic VIP variants in the Blang population from Yunnan Province of China

Chan Zhang, Weiwei Guo, Yujing Cheng, Qi Li, Xin Yang, Run Dai, Linhao Zhu, Wanlu Chen

Mol Genet Genomic Med. 2019 May; 7(5): e574. Published online 2019 Apr 5. doi: 10.1002/mgg3.574

PMCID:: PMC6503013

Abstract Article PDF–1.2M

Select item 63276415.

Identification of differentially expressed non-coding RNAs and mRNAs involved in Qi stagnation and blood stasis syndrome

Guang Chen, Jialiang Gao, Haoqiang He, Chao Liu, Yongmei Liu, Jun Li, Jie Wang

Exp Ther Med. 2019 Feb; 17(2): 1206–1223. Published online 2018 Dec 7. doi: 10.3892/etm.2018.7068

PMCID:: PMC6327641

Abstract Article PDF–3.7M

Select item 63032486.

A genome-wide search for new imprinted genes in the human placenta identifies DSCAM as the first imprinted gene on chromosome 21

Laïla Allach El Khattabi, Stéphanie Backer, Amélie Pinard, Marie-Noëlle Dieudonné, Vassilis Tsatsaris, Daniel Vaiman, Luisa Dandolo, Evelyne Bloch-Gallego, Hélène Jammes, Sandrine Barbaux

Eur J Hum Genet. 2019 Jan; 27(1): 49–60. Published online 2018 Sep 11. doi: 10.1038/s41431-018-0267-3

PMCID:: PMC6303248

Abstract Article PDF–2.1M

Select item 62928947.

The short-sequence design of DNA and its involvement in the 3-D structure of the genome

Guillermo Lamolle, Victor Sabbia, Héctor Musto, Giorgio Bernardi

Sci Rep. 2018; 8: 17820. Published online 2018 Dec 13. doi: 10.1038/s41598-018-35864-9

PMCID:: PMC6292894

Abstract Article PDF–3.4M

Select item 62455978.

SWIFOLD: Smith-Waterman implementation on FPGA with OpenCL for long DNA sequences

Enzo Rucci, Carlos Garcia, Guillermo Botella, Armando De Giusti, Marcelo Naiouf, Manuel Prieto-Matias

BMC Syst Biol. 2018; 12(Suppl 5): 96. Published online 2018 Nov 20. doi: 10.1186/s12918-018-0614-6

PMCID:: PMC6245597

Abstract Article PDF–746K

Select item 62162229.

A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon

Carmen Oleaga-Quintas, Caroline Deswarte, Marcela Moncada-Vélez, Ayse Metin, Indumathi Krishna Rao, Saliha Kanık-Yüksek, Alejandro Nieto-Patlán, Antoine Guérin, Belgin Gülhan, Savita Murthy, Aslınur Özkaya-Parlakay, Laurent Abel, Rubén Martínez-Barricarte, Rebeca Pérez de Diego, Stéphanie Boisson-Dupuis, Xiao-Fei Kong, Jean-Laurent Casanova, Jacinta Bustamante

Hum Mol Genet. 2018 Nov 15; 27(22): 3919–3935. Published online 2018 Aug 3. doi: 10.1093/hmg/ddy275

Correction in:: Hum Mol Genet. 2019 Feb 1; 28(3): 524.

PMCID:: PMC6216222

Abstract Article PDF–15M

Select item 612930810.

DeepSimulator: a deep simulator for Nanopore sequencing

Yu Li, Renmin Han, Chongwei Bi, Mo Li, Sheng Wang, Xin Gao

Bioinformatics. 2018 Sep 1; 34(17): 2899–2908. Published online 2018 Apr 6. doi: 10.1093/bioinformatics/bty223

PMCID:: PMC6129308

Abstract Article PDF–615K

Select item 598317411.

Rapid whole-genome sequencing identifies a novel AIRE variant associated with autoimmune polyendocrine syndrome type 1

Erica Sanford, Kelly Watkins, Shareef Nahas, Michael Gottschalk, Nicole G. Coufal, Lauge Farnaes, David Dimmock, Stephen F. Kingsmore, on behalf of the RCIGM Investigators

Cold Spring Harb Mol Case Stud. 2018 Jun; 4(3): a002485. doi: 10.1101/mcs.a002485

PMCID:: PMC5983174

Abstract Article PDF–830K

Select item 594910712.

Evaluation of extraction methods for methylated cell-free fetal DNA from maternal plasma

Ji Hyae Lim, Bom Yi Lee, Jin Woo Kim, You Jung Han, Jin Hoon Chung, Min Hyoung Kim, Dong Wook Kwak, So Yeon Park, Hee Back Choi, Hyun Mee Ryu

J Assist Reprod Genet. 2018 Apr; 35(4): 637–641. Published online 2018 Feb 8. doi: 10.1007/s10815-018-1114-8

PMCID:: PMC5949107

Abstract Article PDF–353K

Select item 581903313.

Identification of a single nucleotide polymorphism indicative of high risk in acute myocardial infarction

Kavita Shalia, Dhananjaya Saranath, Jaipreet Rayar, Vinod K. Shah, Manoj R. Mashru, Surendra L. Soneji

Indian J Med Res. 2017 Oct; 146(4): 505–513. doi: 10.4103/ijmr.IJMR_1500_15

PMCID:: PMC5819033

Abstract Article PDF–385K

Select item 570715914.

A digenic human immunodeficiency characterized by IFNAR1 and IFNGR2 mutations

Rodrigo Hoyos-Bachiloglu, Janet Chou, Catherine N. Sodroski, Abdallah Beano, Wayne Bainter, Magdalena Angelova, Eman Al Idrissi, Murad K. Habazi, Hamza Ali Alghamdi, Fahd Almanjomi, Mohamed Al Shehri, Nagi Elsidig, Morsi Alaa Eldin, David M. Knipe, Mofareh AlZahrani, Raif S. Geha

J Clin Invest. 2017 Dec 1; 127(12): 4415–4420. Published online 2017 Nov 6. doi: 10.1172/JCI93486

PMCID:: PMC5707159

Abstract Article PDF–1.7M

Select item 563059215.

CRISPR/Cas9-induced transgene insertion and telomere-associated truncation of a single human chromosome for chromosome engineering in CHO and A9 cells

Narumi Uno, Kei Hiramatsu, Katsuhiro Uno, Shinya Komoto, Yasuhiro Kazuki, Mitsuo Oshimura

Sci Rep. 2017; 7: 12739. Published online 2017 Oct 6. doi: 10.1038/s41598-017-10418-7

PMCID:: PMC5630592

Abstract Article PDF–1.3M

Select item 557290716.

Current prospects of type II interferon γ signaling and autoimmunity

Daniel S. Green, Howard A. Young, Julio C. Valencia

J Biol Chem. 2017 Aug 25; 292(34): 13925–13933. Published online 2017 Jun 26. doi: 10.1074/jbc.R116.774745

PMCID:: PMC5572907

Abstract Article PDF–1.0M

Select item 552384017.

Implication of the APP Gene in Intellectual Abilities

Craig Myrum, Oleksii Nikolaienko, Clive R. Bramham, Jan Haavik, Tetyana Zayats

J Alzheimers Dis. 2017; 59(2): 723–735. Prepublished online 2017 Jun 27. Published online 2017 Jul 17. doi: 10.3233/JAD-170049

PMCID:: PMC5523840

Abstract Article PDF–538K

Select item 549507518.

Genome-wide TOP2A DNA cleavage is biased toward translocated and highly transcribed loci

Xiang Yu, James W. Davenport, Karen A. Urtishak, Marie L. Carillo, Sager J. Gosai, Christos P. Kolaris, Jo Ann W. Byl, Eric F. Rappaport, Neil Osheroff, Brian D. Gregory, Carolyn A. Felix

Genome Res. 2017 Jul; 27(7): 1238–1249. doi: 10.1101/gr.211615.116

PMCID:: PMC5495075

Abstract Article PDF–709K

Select item 530787519.

Selective intra-dinucleotide interactions and periodicities of bases separated by K sites: a new vision and tool for phylogeny analyses

Carlos Y. Valenzuela

Biol Res. 2017; 50: 3. Published online 2017 Feb 13. doi: 10.1186/s40659-017-0112-0

PMCID:: PMC5307875

Abstract Article PDF–2.3M

Select item 518162920.

Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotype

Maria Chiara Pelleri, Elena Cicchini, Chiara Locatelli, Lorenza Vitale, Maria Caracausi, Allison Piovesan, Alessandro Rocca, Giulia Poletti, Marco Seri, Pierluigi Strippoli, Guido Cocchi

Hum Mol Genet. 2016 Jun 15; 25(12): 2525–2538. Published online 2016 Apr 22. doi: 10.1093/hmg/ddw116

PMCID:: PMC5181629

Abstract Article PDF–692K

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 44

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity