Mark A Nelson
Overview
Explore the profile of Mark A Nelson including associated specialties, affiliations and a list of published articles.
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Articles
59
Citations
937
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Recent Articles
1.
Dhanalakshmi C, Janakiraman U, Moutal A, Fukunaga K, Khanna R, Nelson M
Neurobiol Dis
. 2024 Aug;
200:106620.
PMID: 39097414
No abstract available.
2.
Bixby B, Vrba L, Lenka J, Oshiro M, Watts G, Hughes T, et al.
Sci Rep
. 2024 Feb;
14(1):2939.
PMID: 38316884
Diagnosis of malignant pleural effusion (MPE) is made by cytological examination of pleural fluid or histological examination of pleural tissue from biopsy. Unfortunately, detection of malignancy using cytology has an...
3.
Bixby B, Vrba L, Lenka J, Oshiro M, Watts G, Hughes T, et al.
Res Sq
. 2023 Oct;
PMID: 37886511
Background: Diagnosis of malignant pleural effusion (MPE) is made by cytological examination of pleural fluid or histological examination of pleural tissue from biopsy. Unfortunately, detection of malignancy using cytology has...
4.
Vrba L, Futscher B, Oshiro M, Watts G, Menashi E, Hu C, et al.
Clin Epigenetics
. 2022 Feb;
14(1):28.
PMID: 35193708
We tested the ability of a novel DNA methylation biomarker set to distinguish metastatic pancreatic cancer cases from benign pancreatic cyst patients and to monitor tumor dynamics using quantitative DNA...
5.
Dhanalakshmi C, Janakiraman U, Moutal A, Fukunaga K, Khanna R, Nelson M
Neurobiol Dis
. 2020 Dec;
149:105224.
PMID: 33359140
The TATA-box binding protein associated factor 1 (TAF1) is part of the TFIID complex that plays a key role during the initiation of transcription. Variants of TAF1 are associated with...
6.
Hurst S, Liktor-Busa E, Moutal A, Parker S, Rice S, Szelinger S, et al.
Neuronal Signal
. 2020 Jul;
2(3):NS20180141.
PMID: 32714589
We investigated the genome of a 5-year-old male who presented with global developmental delay (motor, cognitive, and speech), hypotonia, possibly ataxia, and cerebellar hypoplasia of unknown origin. Whole genome sequencing...
7.
Janakiraman U, Dhanalakshmi C, Yu J, Moutal A, Boinon L, Fukunaga K, et al.
Neurobiol Dis
. 2020 Jul;
143:105006.
PMID: 32622085
T-type calcium channels, in the central nervous system, are involved in the pathogenesis of many neurodegenerative diseases, including TAF1 intellectual disability syndrome (TAF1 ID syndrome). Here, we evaluated the efficacy...
8.
Vrba L, Oshiro M, Kim S, Garland L, Placencia C, Mahadevan D, et al.
Epigenetics
. 2019 Nov;
15(4):419-430.
PMID: 31775567
Identification of cancer-specific methylation of DNA released by tumours can be used for non-invasive diagnostics and monitoring. We previously reported identification of DNA methylation loci specifically hypermethylated in common human...
9.
Janakiraman U, Yu J, Moutal A, Chinnasamy D, Boinon L, Batchelor S, et al.
Neurobiol Dis
. 2019 Jul;
132:104539.
PMID: 31344492
TAF1/MRSX33 intellectual disability syndrome is an X-linked disorder caused by loss-of-function mutations in the TAF1 gene. How these mutations cause dysmorphology, hypotonia, intellectual and motor defects is unknown. Mouse models...
10.
Briehl M, Nelson M, Krupinski E, Erps K, Holcomb M, Weinstein J, et al.
Acad Pathol
. 2017 Jul;
3:2374289516680217.
PMID: 28725783
Faculty members from the Department of Pathology at The University of Arizona College of Medicine-Tucson have offered a 4-credit course on enhanced general pathology for graduate students since 1996. The...