R Harnik
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Explore the profile of R Harnik including associated specialties, affiliations and a list of published articles.
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9
Citations
873
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Recent Articles
1.
Romanenko A, Harnik R, Grassellino A, Pilipenko R, Pischalnikov Y, Liu Z, et al.
Phys Rev Lett
. 2023 Jul;
130(26):261801.
PMID: 37450797
We conduct the first "light-shining-through-wall" (LSW) search for dark photons using two state-of-the-art high-quality-factor superconducting radio frequency (SRF) cavities -Dark SRF-and report the results of its pathfinder run. Our new...
2.
Acciarri R, Adams C, Baller B, Basque V, Cavanna F, Co R, et al.
Phys Rev Lett
. 2023 Jun;
130(22):221802.
PMID: 37327426
We present the results of a search for heavy QCD axions performed by the ArgoNeuT experiment at Fermilab. We search for heavy axions produced in the NuMI neutrino beam target...
3.
Acciarri R, Adams C, Asaadi J, Baller B, Bolton T, Bromberg C, et al.
Phys Rev Lett
. 2020 Apr;
124(13):131801.
PMID: 32302167
A search for millicharged particles, a simple extension of the standard model, has been performed with the ArgoNeuT detector exposed to the Neutrinos at the Main Injector beam at Fermilab....
4.
Aaltonen T, Alvarez Gonzalez B, Amerio S, Amidei D, Anastassov A, Annovi A, et al.
Phys Rev Lett
. 2012 Sep;
108(21):211804.
PMID: 23003242
We present the results of a search for dark matter production in the monojet signature. We analyze a sample of Tevatron pp[over ¯] collisions at √s=1.96 TeV corresponding to an...
5.
Gilad S, Khosravi R, Harnik R, Ziv Y, Shkedy D, Galanty Y, et al.
Hum Mutat
. 1998 Feb;
11(1):69-75.
PMID: 9450906
Ataxia-telangiectasia (A-T) is an autosomal recessive disorder characterized by neurodegeneration, immunodeficiency, cancer predisposition, and radiation sensitivity. The responsible gene, ATM, has an extensive genomic structure and encodes a large transcript...
6.
Gilad S, Bar-Shira A, Harnik R, Shkedy D, Ziv Y, Khosravi R, et al.
Hum Mol Genet
. 1996 Dec;
5(12):2033-7.
PMID: 8968760
The ATM gene is responsible for the autosomal recessive disorder ataxia-telangiectasia (A-T), characterized by cerebellar degeneration, immunodeficiency and cancer predisposition. A-T carriers were reported to be moderately cancer-prone. A wide...
7.
PECKER I, Avraham K, Gilbert D, Savitsky K, Rotman G, Harnik R, et al.
Genomics
. 1996 Jul;
35(1):39-45.
PMID: 8661102
Atm, the mouse homolog of the human ATM gene defective in ataxia-telangiectasia (A-T), has been identified. The entire coding sequence of the Atm transcript was cloned and found to contain...
8.
Gilad S, Khosravi R, Shkedy D, Uziel T, Ziv Y, Savitsky K, et al.
Hum Mol Genet
. 1996 Apr;
5(4):433-9.
PMID: 8845835
Ataxia-telangiectasia (A-T) is an autosomal recessive disorder involving cerebellar degeneration, immunodeficiency, chromosomal instability, radiosensitivity and cancer predisposition. The responsible gene, ATM, was recently identified by positional cloning and found to...
9.
Savitsky K, Bar-Shira A, Gilad S, Rotman G, Ziv Y, Vanagaite L, et al.
Science
. 1995 Jun;
268(5218):1749-53.
PMID: 7792600
A gene, ATM, that is mutated in the autosomal recessive disorder ataxia telangiectasia (AT) was identified by positional cloning on chromosome 11q22-23. AT is characterized by cerebellar degeneration, immunodeficiency, chromosomal...