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NDP-AS1 gene

Known as: NDP antisense RNA 1, NDP-AS1 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Energy Modeling of Neighbor Discovery in Bluetooth Low Energy Networks
Given that current Internet of Things (IoT) applications employ many different sensors to provide information, a large number of… 
2018
2018
Extended-spectrum beta-lactamase detection by extended-spectrum beta-lactamase-Nordmann/Dortet/Poirel test: Where time is the essence
Background: Extended-spectrum beta-lactamase (ESBL)-producing strains are causing an increasing problem worldwide. Infection… 
2017
2017
HUBUNGAN ANTARA DERAJAT NEUROPATI PERIFER DIABETIKDENGAN KUALITAS HIDUP PADA PASIEN DM TIPE 2DI POLIKLINIK DALAM RSUD PANEMBAHANSENOPATI BANTUL
Latar Belakang: Diabetes mellitus (DM) adalah penyakit kronis yang disebabkan karena organ pankreas tidak bisa mencukupi… 
2016
2016
Reinventing Nilai NDP Dalam Diri Kita
Jika gagasan tentang revolusi diterapkan di wialayah nilai-nilai, maka Nilai Dasar Perjuangan (NDP) HMI merupakan revolusi nilai… 
2016
2016
ERITROSIT BERINTI SEBAGAI ALAT PENUNJANG DIAGNOSIS ASIDOSIS PADA ASFIKSIA NEONATORUM
Latar belakang: Asfiksia neonatorum merupakan penyebab utama kematian neonatus sebesar 19% dari lima juta bayi lahir hidup di… 
2014
2014
6LoWPAN (IPv6 over low-power wireless personal area networks)-based NDP (neighbor discovery protocol)
The invention discloses a 6LoWPAN (IPv6 over low-power wireless personal area networks)-based NDP (neighbor discovery protocol… 
Review
2009
Review
2009
Enzymatic synthesis of TDP-deoxysugars.
2004
2004
Radioiodination of Rhenium Cyclized α-Melanocyte-Stimulating Hormone Resulting in Enhanced Radioactivity Localization and Retention in Melanoma
Radiohalogenated α-melanocyte-stimulating hormone (α-MSH) analogs were proposed for melanoma imaging and potential radiotherapy… 
1993
1993
転移抑制遺伝子 NDP キナーゼ/nm23 遺伝子産物発現からみた膵腫瘍の生物学的悪性度
1992
1992
The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.
Norrie disease is a human X-linked recessive disorder of unknown etiology characterized by congenital blindness, sensory neural… 
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