NATIONAL UNDERWRITING SERVICES
National Underwriting Services specalizes in underwriting, accounting, sold case documentation and claims administration services.
NATIONAL UNDERWRITING SERVICES
Social Links:
Industry:
Accounting Consulting Financial Services
Founded:
1985-01-01
Address:
Helotes, Texas, United States
Country:
United States
Website Url:
http://www.nus1.com
Status:
Active
Contact:
+1-210-695-2381
Technology used in webpage:
Viewport Meta IPhone / Mobile Compatible SPF SSL By Default Google Font API Apache Microsoft Exchange Online Office 365 Mail ReCAPTCHA Apache 2.4
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National Tax and Financial Services
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Official Site Inspections
http://www.nus1.com
- Host name: ec2-35-170-92-192.compute-1.amazonaws.com
- IP address: 35.170.92.192
- Location: Ashburn United States
- Latitude: 39.0481
- Longitude: -77.4728
- Metro Code: 511
- Timezone: America/New_York
- Postal: 20149
More informations about "National Underwriting Services"
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What is NUS1? - Nus1 Foundation
NUS1 is a gene on chromosome 6q22.1. Mutations within the NUS1 gene lead to a diagnosis of NUS1 genetic disorder. If both copies of the NUS1 gene bear a mutation, a severe, ultra-rare …See details»
About Us - Nus1 Foundation
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If you or a loved one has been recently diagnosed with a DHDDS or NUS1 mutation please visit our private Facebook group Cure DHDDS and NUS1 community for support or advice. Watch our short film to learn more...See details»
Lysosomal cholesterol accumulation contributes to the movement ...
Mar 17, 2021 · We present three patients with de novo heterozygous variants in NUS1 that cause a complex movement disorder, define pathogenic mechanisms in cells and zebrafish, and …See details»
SC Family Finds Hope in Research Breakthrough for …
Mar 22, 2021 · Initial genetic tests were normal, until at 12 years of age, her geneticist, Dr. Mike Lyons of the Greenwood Genetic Center’s (GGC’s) Charleston SC office, suggested whole exome sequencing, which analyzes all …See details»
Replication assessment of NUS1 variants in Parkinson’s disease
Here, as part of the International Parkinson’s Disease Genomics Consortium, we have leveraged large-scale PD case-control cohorts to comprehensively assess damaging NUS1 variants in …See details»
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Discover how NUS1 Research, a leading Medical Research Organization, is advancing the science for better health using innovative methods like Zebrafish.See details»
Lysosomal Cholesterol Accumulation Contributes to the …
We show that de novo NUS1 variants reduce NgBR and Niemann-Pick type C2 (NPC2) protein amount, impair dolichol biosynthesis, and cause lysosomal cholesterol accumulation. …See details»
NUS1 Variants Cause Lennox-Gastaut Syndrome Related to
Mar 23, 2024 · Although several loss-of-function variants of NUS1 have been identified in patients with developmental and epileptic encephalopathy (DEE), the role of the NUS1 variant in …See details»
Cure DHDDS
Welcome to Cure DHDDS USA a charity set up to raise awareness, support families and help drive research into the ultra-rare DHDDS gene mutations. CURE DHDDS IS POWERED BY RARE VILLAGE 2023.See details»
NUS1 curation results for Dosage Sensitivity - Clinical Genome
Individuals with de novo, heterozygous, loss-of-function variants in NUS1 have been reported in association with autosomal dominant intellectual disability with seizures.See details»
Recurrent NUS1 canonical splice donor site mutation in two …
Oct 27, 2019 · Our study strongly supports the finding that this recurrent, de novo, variant in NUS1 causes developmental and epileptic encephalopathy with involuntary movement, ataxia …See details»
Resources - Nus1 Foundation
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NUS1 Gene - GeneCards | NGBR Protein | NGBR Antibody
Oct 2, 2024 · NUS1 (NUS1 Dehydrodolichyl Diphosphate Synthase Subunit) is a Protein Coding gene. Diseases associated with NUS1 include Congenital Disorder Of Glycosylation, Type Iaa …See details»
Case series; NUS1 deletions cause a progressive ... - ScienceDirect
Nov 20, 2024 · We used PubMed to search for all papers with search terms ‘NUS1 gene deletions’ and then followed an iterative search strategy using references from key papers to …See details»
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Here we report a new case presenting with epilepsy, myoclonus, mild cerebellar ataxia and intellectual disability carrying a novel heterozygous NUS1 missense variant. We evaluated a …See details»
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The NUS1 Foundation is here to help you navigate the complex world of caring for a loved one with NUS1 Genetic Disorder. This page is updated regularly to continulously contribute new …See details»
NUS1 DEHYDRODOLICHYL DIPHOSPHATE SYNTHASE SUBUNIT; …
Aug 27, 2021 · The NUS1 gene encodes a membrane protein that is a subunit of cis-prenyltransferase (cis-PTase) and is involved in the synthesis of dolichol, which is necessary …See details»
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Get involved and be a part of the hope for the future of those affected by NUS1 disorders. Below we have a few ways to get more involved as a caretaker, friend, family or community member …See details»