287 related articles for article (PubMed ID: 32902713)
1. Impacts of genomic networks governed by human-specific regulatory sequences and genetic loci harboring fixed human-specific neuro-regulatory single nucleotide mutations on phenotypic traits of modern humans.
Glinsky GV
Chromosome Res; 2020 Dec; 28(3-4):331-354. PubMed ID: 32902713
[TBL] [Abstract][Full Text] [Related]
2. Molecular diversity and phenotypic pleiotropy of ancient genomic regulatory loci derived from human endogenous retrovirus type H (HERVH) promoter LTR7 and HERVK promoter LTR5_Hs and their contemporary impacts on pathophysiology of Modern Humans.
Glinsky GV
Mol Genet Genomics; 2022 Nov; 297(6):1711-1740. PubMed ID: 36121513
[TBL] [Abstract][Full Text] [Related]
3. A Catalogue of 59,732 Human-Specific Regulatory Sequences Reveals Unique-to-Human Regulatory Patterns Associated with Virus-Interacting Proteins, Pluripotency, and Brain Development.
Glinsky GV
DNA Cell Biol; 2020 Jan; 39(1):126-143. PubMed ID: 31730374
[TBL] [Abstract][Full Text] [Related]
4. Mechanistically Distinct Pathways of Divergent Regulatory DNA Creation Contribute to Evolution of Human-Specific Genomic Regulatory Networks Driving Phenotypic Divergence of Homo sapiens.
Glinsky GV
Genome Biol Evol; 2016 Sep; 8(9):2774-88. PubMed ID: 27503290
[TBL] [Abstract][Full Text] [Related]
5. Contribution of transposable elements and distal enhancers to evolution of human-specific features of interphase chromatin architecture in embryonic stem cells.
Glinsky GV
Chromosome Res; 2018 Mar; 26(1-2):61-84. PubMed ID: 29335803
[TBL] [Abstract][Full Text] [Related]
6. Genomics-Guided Drawing of Molecular and Pathophysiological Components of Malignant Regulatory Signatures Reveals a Pivotal Role in Human Diseases of Stem Cell-Associated Retroviral Sequences and Functionally-Active hESC Enhancers.
Glinsky GV
Front Oncol; 2021; 11():638363. PubMed ID: 33869024
[TBL] [Abstract][Full Text] [Related]
7. Transposable Elements and DNA Methylation Create in Embryonic Stem Cells Human-Specific Regulatory Sequences Associated with Distal Enhancers and Noncoding RNAs.
Glinsky GV
Genome Biol Evol; 2015 May; 7(6):1432-54. PubMed ID: 25956794
[TBL] [Abstract][Full Text] [Related]
8. Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness.
Kowalczyk A; Chikina M; Clark N
Elife; 2022 Nov; 11():. PubMed ID: 36342464
[TBL] [Abstract][Full Text] [Related]
9. Human-specific histone methylation signatures at transcription start sites in prefrontal neurons.
Shulha HP; Crisci JL; Reshetov D; Tushir JS; Cheung I; Bharadwaj R; Chou HJ; Houston IB; Peter CJ; Mitchell AC; Yao WD; Myers RH; Chen JF; Preuss TM; Rogaev EI; Jensen JD; Weng Z; Akbarian S
PLoS Biol; 2012; 10(11):e1001427. PubMed ID: 23185133
[TBL] [Abstract][Full Text] [Related]
10. Activation of endogenous human stem cell-associated retroviruses (SCARs) and therapy-resistant phenotypes of malignant tumors.
Glinsky GV
Cancer Lett; 2016 Jul; 376(2):347-59. PubMed ID: 27084523
[TBL] [Abstract][Full Text] [Related]
11. Extensive evolutionary changes in regulatory element activity during human origins are associated with altered gene expression and positive selection.
Shibata Y; Sheffield NC; Fedrigo O; Babbitt CC; Wortham M; Tewari AK; London D; Song L; Lee BK; Iyer VR; Parker SC; Margulies EH; Wray GA; Furey TS; Crawford GE
PLoS Genet; 2012 Jun; 8(6):e1002789. PubMed ID: 22761590
[TBL] [Abstract][Full Text] [Related]
12. Shared regulatory sites are abundant in the human genome and shed light on genome evolution and disease pleiotropy.
Tong P; Monahan J; Prendergast JG
PLoS Genet; 2017 Mar; 13(3):e1006673. PubMed ID: 28282383
[TBL] [Abstract][Full Text] [Related]
13. Novel Bioinformatics Approach Identifies Transcriptional Profiles of Lineage-Specific Transposable Elements at Distinct Loci in the Human Dorsolateral Prefrontal Cortex.
Guffanti G; Bartlett A; Klengel T; Klengel C; Hunter R; Glinsky G; Macciardi F
Mol Biol Evol; 2018 Oct; 35(10):2435-2453. PubMed ID: 30053206
[TBL] [Abstract][Full Text] [Related]
14. Systematic analysis of chromatin interactions at disease associated loci links novel candidate genes to inflammatory bowel disease.
Meddens CA; Harakalova M; van den Dungen NA; Foroughi Asl H; Hijma HJ; Cuppen EP; Björkegren JL; Asselbergs FW; Nieuwenhuis EE; Mokry M
Genome Biol; 2016 Nov; 17(1):247. PubMed ID: 27903283
[TBL] [Abstract][Full Text] [Related]
15. Many inflammatory bowel disease risk loci include regions that regulate gene expression in immune cells and the intestinal epithelium.
Mokry M; Middendorp S; Wiegerinck CL; Witte M; Teunissen H; Meddens CA; Cuppen E; Clevers H; Nieuwenhuis EE
Gastroenterology; 2014 Apr; 146(4):1040-7. PubMed ID: 24333384
[TBL] [Abstract][Full Text] [Related]
16. scGRNom: a computational pipeline of integrative multi-omics analyses for predicting cell-type disease genes and regulatory networks.
Jin T; Rehani P; Ying M; Huang J; Liu S; Roussos P; Wang D
Genome Med; 2021 May; 13(1):95. PubMed ID: 34044854
[TBL] [Abstract][Full Text] [Related]
17. Single cell genomics reveals activation signatures of endogenous SCAR's networks in aneuploid human embryos and clinically intractable malignant tumors.
Glinsky GV
Cancer Lett; 2016 Oct; 381(1):176-93. PubMed ID: 27497790
[TBL] [Abstract][Full Text] [Related]
18. Genetic colocalization atlas points to common regulatory sites and genes for hematopoietic traits and hematopoietic contributions to disease phenotypes.
Thom CS; Voight BF
BMC Med Genomics; 2020 Jun; 13(1):89. PubMed ID: 32600345
[TBL] [Abstract][Full Text] [Related]
19. Human-specific loss of regulatory DNA and the evolution of human-specific traits.
McLean CY; Reno PL; Pollen AA; Bassan AI; Capellini TD; Guenther C; Indjeian VB; Lim X; Menke DB; Schaar BT; Wenger AM; Bejerano G; Kingsley DM
Nature; 2011 Mar; 471(7337):216-9. PubMed ID: 21390129
[TBL] [Abstract][Full Text] [Related]
20. Three-dimensional genome rewiring in loci with human accelerated regions.
Keough KC; Whalen S; Inoue F; Przytycki PF; Fair T; Deng C; Steyert M; Ryu H; Lindblad-Toh K; Karlsson E; ; Nowakowski T; Ahituv N; Pollen A; Pollard KS
Science; 2023 Apr; 380(6643):eabm1696. PubMed ID: 37104607
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
