Pasano Bojang Jr
Overview
Explore the profile of Pasano Bojang Jr including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
247
Followers
0
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Recent Articles
1.
Guerra S, Vasquez M, Bojang Jr P, Ramos I, Sherrill D, Martinez F, et al.
ERJ Open Res
. 2019 Nov;
5(4).
PMID: 31777752
http://bit.ly/2ZEIjNv.
2.
Bojang Jr P, Ramos K
Mol Oncol
. 2018 May;
12(8):1342-1357.
PMID: 29845737
Long interspersed nuclear element-1 (LINE-1 or L1) reactivation is linked to poor prognosis in non-small-cell lung carcinoma (NSCLC), but the molecular bases of this response remain largely unknown. In this...
3.
Bojang Jr P, Anderton M, Roberts R, Ramos K
Genomics
. 2014 Jul;
104(2):96-104.
PMID: 25043885
Long interspersed nuclear elements (Line-1 or L1s) account for ~17% of the human genome. While the majority of human L1s are inactive, ~80-100 elements remain retrotransposition competent and mobilize through...
4.
Bojang Jr P, Ramos K
Cancer Treat Rev
. 2013 Jul;
40(1):153-69.
PMID: 23831234
Genetic mutations and gross structural defects in the DNA sequence permanently alter genetic loci in ways that significantly disrupt gene function. In sharp contrast, genes modified by aberrant epigenetic modifications...
5.
Bojang Jr P, Roberts R, Anderton M, Ramos K
Mol Oncol
. 2013 May;
7(4):812-25.
PMID: 23648019
Long Interspersed Nuclear Element-1 (LINE-1 or L1) is an autonomous, mobile element within the human genome that transposes via a "copy and paste" mechanism and relies upon L1-encoded endonuclease and...
6.
Peachey N, Pearring J, Bojang Jr P, Hirschtritt M, Sturgill-Short G, Ray T, et al.
J Neurophysiol
. 2012 Aug;
108(9):2442-51.
PMID: 22896717
Mutations in TRPM1 are found in humans with an autosomal recessive form of complete congenital stationary night blindness (cCSNB). The Trpm1(-/-) mouse has been an important animal model for this...
7.
Bojang Jr P, Gregg R
PLoS One
. 2012 Apr;
7(4):e33137.
PMID: 22485138
Nyctalopin is a small leucine rich repeat proteoglycan (SLRP) whose function is critical for normal vision. The absence of nyctalopin results in the complete form of congenital stationary night blindness....
8.
Peachey N, Ray T, Florijn R, Rowe L, Sjoerdsma T, Contreras-Alcantara S, et al.
Am J Hum Genet
. 2012 Feb;
90(2):331-9.
PMID: 22325362
Complete congenital stationary night blindness (cCSNB) is a clinically and genetically heterogeneous group of retinal disorders characterized by nonprogressive impairment of night vision, absence of the electroretinogram (ERG) b-wave, and...
9.
Pearring J, Bojang Jr P, Shen Y, Koike C, Furukawa T, Nawy S, et al.
J Neurosci
. 2011 Jul;
31(27):10060-6.
PMID: 21734298
Expression of channels to specific neuronal sites can critically impact their function and regulation. Currently, the molecular mechanisms underlying this targeting and intracellular trafficking of transient receptor potential (TRP) channels...