U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 88

1.
Genotyping and Copy Number Analysis of Immunoglobin Heavy Chain Variable Genes Using Long Reads
Michael Ford, Ehsan Haghshenas, Corey T. Watson, S. Cenk Sahinalp
iScience. 2020 Mar 27; 23(3): 100883. Published online 2020 Feb 4. doi: 10.1016/j.isci.2020.100883
Correction in:
iScience. 2020 Sep 25; 23(9): 101508.
PMCID:
PMC7044747
ArticlePDF–2.0M
2.
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
ArticlePDF–1.2M
3.
LncRNA DLX6‐AS1 increases the expression of HIF‐1α and promotes the malignant phenotypes of nasopharyngeal carcinoma cells via targeting MiR‐199a‐5p
Bin Yang, Lin Jia, Hui Ren, Caibao Jin, Qingrong Ren, Haiyuan Zhang, Desheng Hu, Hao Zhang, Liu Hu, Tao Xie
Mol Genet Genomic Med. 2020 Jan; 8(1): e1017. Published online 2019 Nov 29. doi: 10.1002/mgg3.1017
PMCID:
PMC6978402
ArticlePDF–1.2M
4.
Abnormalities in the genes that encode Large Amino Acid Transporters increase the risk of Autism Spectrum Disorder
Lauren Cascio, Chin‐Fu Chen, Rini Pauly, Sujata Srikanth, Kelly Jones, Cindy D. Skinner, Roger E. Stevenson, Charles E. Schwartz, Luigi Boccuto
Mol Genet Genomic Med. 2020 Jan; 8(1): e1036. Published online 2019 Nov 7. doi: 10.1002/mgg3.1036
PMCID:
PMC6978257
ArticlePDF–826K
5.
Lower S-adenosylmethionine levels and DNA hypomethylation of placental growth factor (PlGF) in placental tissue of early-onset preeclampsia-complicated pregnancies
Sandra G. Heil, Emilie M. Herzog, Pieter H. Griffioen, Bertrand van Zelst, Sten P. Willemsen, Yolanda B. de Rijke, Regine P. M. Steegers-Theunissen, Eric A. P. Steegers
PLoS One. 2019; 14(12): e0226969. Published online 2019 Dec 30. doi: 10.1371/journal.pone.0226969
PMCID:
PMC6936822
ArticlePDF–541K
6.
Lnc-TCL6 is a potential biomarker for early diagnosis and grade in liver-cirrhosis patients
Lei-Jia Li, Xiao-Ying Wu, Si-Wei Tan, Zi-Jun Xie, Xue-Mei Pan, Shun-Wen Pan, Wu-Ri-Na Bai, Hai-Jiao Li, Hui-Ling Liu, Jie Jiang, Bin Wu
Gastroenterol Rep (Oxf) 2019 Dec; 7(6): 434–443. Published online 2019 Oct 11. doi: 10.1093/gastro/goz050
PMCID:
PMC6911997
ArticlePDF–1.0M
7.
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability
Anna Lindstrand, Jesper Eisfeldt, Maria Pettersson, Claudia M. B. Carvalho, Malin Kvarnung, Giedre Grigelioniene, Britt-Marie Anderlid, Olof Bjerin, Peter Gustavsson, Anna Hammarsjö, Patrik Georgii-Hemming, Erik Iwarsson, Maria Johansson-Soller, Kristina Lagerstedt-Robinson, Agne Lieden, Måns Magnusson, Marcel Martin, Helena Malmgren, Magnus Nordenskjöld, Ameli Norling, Ellika Sahlin, Henrik Stranneheim, Emma Tham, Josephine Wincent, Sofia Ygberg, Anna Wedell, Valtteri Wirta, Ann Nordgren, Johanna Lundin, Daniel Nilsson
Genome Med. 2019; 11: 68. Published online 2019 Nov 7. doi: 10.1186/s13073-019-0675-1
PMCID:
PMC6836550
ArticlePDF–2.5M
8.
MicroRNA-300: A Transcellular Mediator in Exosome Regulates Melanoma Progression
Long Chen, Vega Windy Karisma, Huawen Liu, Li Zhong
Front Oncol. 2019; 9: 1005. Published online 2019 Oct 15. doi: 10.3389/fonc.2019.01005
PMCID:
PMC6803498
ArticlePDF–3.0M
9.
Functional characterization of a SNP (F51S) found in human alpha 1‐antitrypsin
Hong‐Nhung Trinh, Sei‐Heon Jang, ChangWoo Lee
Mol Genet Genomic Med. 2019 Aug; 7(8): e819. Published online 2019 Jun 28. doi: 10.1002/mgg3.819
PMCID:
PMC6687665
ArticlePDF–924K
10.
Association of NTCP polymorphisms with clinical outcome of hepatitis B infection in Thai individuals
Natthaya Chuaypen, Nongnaput Tuyapala, Nutcha Pinjaroen, Sunchai Payungporn, Pisit Tangkijvanich
BMC Med Genet. 2019; 20: 87. Published online 2019 May 22. doi: 10.1186/s12881-019-0823-x
PMCID:
PMC6532194
ArticlePDF–625K
11.
Correlation of Thyroid Transcription Factor-1 Expression with EGFR Mutations in Non-Small-Cell Lung Cancer: A Meta-Analysis
Hyeong Su Kim, Jung Han Kim, Boram Han, Dae Ro Choi
Medicina (Kaunas) 2019 Feb; 55(2): 41. Published online 2019 Feb 7. doi: 10.3390/medicina55020041
PMCID:
PMC6410251
ArticlePDF–3.0M
12.
A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture?
Roberta Milone, Riccardo Masson, Caterina Di Cosmo, Massimo Tonacchera, Veronica Bertini, Andrea Guzzetta, Roberta Battini
Child Neurol Open. 2019; 6: 2329048X19828881. Published online 2019 Feb 12. doi: 10.1177/2329048X19828881
PMCID:
PMC6376510
ArticlePDF–159K
13.
Alpha-1 Antitrypsin Deficiency as an Incidental Finding in Clinical Genetic Testing
Craig P. Hersh, Edward J. Campbell, Lauren R. Scott, Benjamin A. Raby
Am J Respir Crit Care Med. 2019 Jan 15; 199(2): 246–248. Published online 2019 Jan 15. doi: 10.1164/rccm.201809-1679LE
PMCID:
PMC6353005
ArticlePDF–455K
14.
The Relationship between Nkx2.1 and DNA Oxidative Damage Repair in Nickel Smelting Workers: Jinchang Cohort Study
Zhiyuan Cheng, Ning Cheng, Dian Shi, Xiaoyu Ren, Ting Gan, Yana Bai, Kehu Yang
Int J Environ Res Public Health. 2019 Jan; 16(1): 120. Published online 2019 Jan 4. doi: 10.3390/ijerph16010120
PMCID:
PMC6339211
ArticlePDF–1.6M
15.
FoxA1 and FoxA2 drive gastric differentiation and suppress squamous identity in NKX2-1-negative lung cancer
Soledad A Camolotto, Shrivatsav Pattabiraman, Timothy L Mosbruger, Alex Jones, Veronika K Belova, Grace Orstad, Mitchell Streiff, Lydia Salmond, Chris Stubben, Klaus H Kaestner, Eric L Snyder
eLife. 2018; 7: e38579. Published online 2018 Nov 26. doi: 10.7554/eLife.38579
PMCID:
PMC6303105
ArticlePDF–9.2M
16.
V-ATPases and osteoclasts: ambiguous future of V-ATPases inhibitors in osteoporosis
Xiaohong Duan, Shaoqing Yang, Lei Zhang, Tielin Yang
Theranostics. 2018; 8(19): 5379–5399. Published online 2018 Oct 26. doi: 10.7150/thno.28391
PMCID:
PMC6276090
ArticlePDF–1.2M
17.
Methylome analysis of thyroid ectopy shows no disease-specific DNA methylation signature
Satoshi Narumi, Keiko Matsubara, Tomohiro Ishii, Tomonobu Hasegawa
Clin Pediatr Endocrinol. 2018; 27(4): 235–238. Published online 2018 Oct 30. doi: 10.1297/cpe.27.235
PMCID:
PMC6207800
ArticlePDF–583K
18.
High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism
Nina Makretskaya, Olga Bezlepkina, Anna Kolodkina, Alexey Kiyaev, Evgeny V. Vasilyev, Vasily Petrov, Svetlana Kalinenkova, Oleg Malievsky, Ivan I. Dedov, Anatoly Tiulpakov
PLoS One. 2018; 13(9): e0204323. Published online 2018 Sep 21. doi: 10.1371/journal.pone.0204323
PMCID:
PMC6150524
ArticlePDF–2.0M
19.
NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement
Péter Balicza, Zoltán Grosz, Viktor Molnár, Anett Illés, Dora Csabán, Andras Gézsi, Lívia Dézsi, Dénes Zádori, László Vécsei, Mária Judit Molnár
Front Genet. 2018; 9: 335. Published online 2018 Aug 22. doi: 10.3389/fgene.2018.00335
PMCID:
PMC6113386
ArticlePDF–575K
20.
Mutational Analysis of Oncogenic AKT1 Gene Associated with Breast Cancer Risk in the High Altitude Ecuadorian Mestizo Population
Andrés López-Cortés, Paola E. Leone, Byron Freire-Paspuel, Nathaly Arcos-Villacís, Patricia Guevara-Ramírez, Felipe Rosales, César Paz-y-Miño
Biomed Res Int. 2018; 2018: 7463832. Published online 2018 Jul 3. doi: 10.1155/2018/7463832
PMCID:
PMC6051326
ArticlePDF–837K

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

You are here: NCBI > Literature > PubMed Central (PMC)
Support Center