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Itamar Harel is an Israeli scientist best known for his contributions to the field of Experimental [[Ageing|Aging]] Research. He is faculty member in the Department of Genetics at the Alexander Silberman Institute of Life sciences, the [[Hebrew University of Jerusalem]], [[Israel]].
Itamar Harel is an Israeli scientist known for his contributions to the field of Experimental [[Ageing|Aging]] Research. He is faculty member in the Department of Genetics at the Alexander Silberman Institute of Life sciences, the [[Hebrew University of Jerusalem]], [[Israel]].


== Research ==
== Research ==
Itamar Harel is a researcher in the field of biology, specifically known for his work in the areas of aging and disease (reviewed in<ref>{{cite journal |last1=Marx |first1=Vivien |title=Aging research comes of age |journal=Nature Methods |date=January 2024 |volume=21 |issue=1 |pages=11–15 |doi=10.1038/s41592-023-02140-2 |pmid=38167657 |url=https://www.nature.com/articles/s41592-023-02140-2 |language=en |issn=1548-7105}}</ref><ref>{{cite journal |last1=Dance |first1=Amber |title=Live fast, die young |journal=Nature |date=July 2016 |volume=535 |issue=7612 |pages=453–455 |doi=10.1038/535453a |pmid=27443744 |bibcode=2016Natur.535..453D |url=https://www.nature.com/articles/535453a |language=en |issn=1476-4687}}</ref><ref>{{cite journal |last1=Singh |first1=Param Priya |last2=Demmitt |first2=Brittany A. |last3=Nath |first3=Ravi D. |last4=Brunet |first4=Anne |title=The Genetics of Aging: A Vertebrate Perspective |journal=Cell |date=March 2019 |volume=177 |issue=1 |pages=200–220 |doi=10.1016/j.cell.2019.02.038|pmid=30901541 |pmc=7592626 }}</ref><ref>{{cite journal |last1=Wang |first1=Adrienne M. |last2=Promislow |first2=Daniel E.L. |last3=Kaeberlein |first3=Matt |title=Fertile Waters for Aging Research |journal=Cell |date=February 2015 |volume=160 |issue=5 |pages=814–815 |doi=10.1016/j.cell.2015.02.026|pmid=25723160 }}</ref>). Harel's research focuses on understanding the mechanisms of aging and [[longevity]], with a particular interest in using the emerging African turquoise [[killifish]] (''[[Nothobranchius furzeri]]'') model to study these processes.<ref>{{Cite journal |last=Harel |first=Itamar |date=October 2022 |title=The turquoise killifish |url=https://www.nature.com/articles/s41592-022-01631-y |journal=Nature Methods |language=en |volume=19 |issue=10 |pages=1150–1151 |doi=10.1038/s41592-022-01631-y |pmid=36203025 |issn=1548-7091}}</ref><ref>{{cite news |last1=Zimmer |first1=Carl |title=In Short-Lived Fish, Secrets to Aging |url=https://www.nytimes.com/2015/03/03/science/in-short-lived-fish-secrets-to-aging.html |work=The New York Times |date=27 February 2015}}</ref><ref name=":0">{{Cite web |title=How germline regulation, sex differences impact the lifespan of male, female vertebrates |date=15 May 2024 |url=https://www.jpost.com/science/article-801200}}</ref><ref name=":1">{{Cite web |title=AMP biosynthesis key to longevity and metabolic health in vertebrates |url=https://www.eurekalert.org/news-releases/995311}}</ref> His work aims to uncover the biological pathways that influence aging and to develop potential interventions to promote healthy aging.
Itamar Harel is a researcher in the field of biology, specifically known for his work in the areas of aging and disease (reviewed in<ref>{{cite journal |last1=Marx |first1=Vivien |title=Aging research comes of age |journal=Nature Methods |date=January 2024 |volume=21 |issue=1 |pages=11–15 |doi=10.1038/s41592-023-02140-2 |pmid=38167657 |url=https://www.nature.com/articles/s41592-023-02140-2 |language=en |issn=1548-7105}}</ref><ref>{{cite journal |last1=Dance |first1=Amber |title=Live fast, die young |journal=Nature |date=July 2016 |volume=535 |issue=7612 |pages=453–455 |doi=10.1038/535453a |pmid=27443744 |bibcode=2016Natur.535..453D |url=https://www.nature.com/articles/535453a |language=en |issn=1476-4687}}</ref><ref>{{cite journal |last1=Singh |first1=Param Priya |last2=Demmitt |first2=Brittany A. |last3=Nath |first3=Ravi D. |last4=Brunet |first4=Anne |title=The Genetics of Aging: A Vertebrate Perspective |journal=Cell |date=March 2019 |volume=177 |issue=1 |pages=200–220 |doi=10.1016/j.cell.2019.02.038|pmid=30901541 |pmc=7592626 }}</ref><ref>{{cite journal |last1=Wang |first1=Adrienne M. |last2=Promislow |first2=Daniel E.L. |last3=Kaeberlein |first3=Matt |title=Fertile Waters for Aging Research |journal=Cell |date=February 2015 |volume=160 |issue=5 |pages=814–815 |doi=10.1016/j.cell.2015.02.026|pmid=25723160 }}</ref>). Harel's research focuses on understanding the mechanisms of aging and [[longevity]], with a particular interest in using the emerging African turquoise [[killifish]] (''[[Nothobranchius furzeri]]'') model to study these processes.<ref>{{Cite journal |last=Harel |first=Itamar |date=October 2022 |title=The turquoise killifish |url=https://www.nature.com/articles/s41592-022-01631-y |journal=Nature Methods |language=en |volume=19 |issue=10 |pages=1150–1151 |doi=10.1038/s41592-022-01631-y |pmid=36203025 |issn=1548-7091}}</ref><ref>{{cite news |last1=Zimmer |first1=Carl |title=In Short-Lived Fish, Secrets to Aging |url=https://www.nytimes.com/2015/03/03/science/in-short-lived-fish-secrets-to-aging.html |work=The New York Times |date=27 February 2015}}</ref><ref name=":0">{{Cite web |title=How germline regulation, sex differences impact the lifespan of male, female vertebrates |date=15 May 2024 |url=https://www.jpost.com/science/article-801200}}</ref><ref name=":1">{{Cite web |title=AMP biosynthesis key to longevity and metabolic health in vertebrates |url=https://www.eurekalert.org/news-releases/995311}}</ref> His work aims to uncover the biological pathways that influence aging and to develop potential interventions to promote healthy aging.


Harel pioneered a genetic platform in the naturally short-lived turquoise killifish<ref>{{Cite journal |last1=Harel |first1=Itamar |last2=Benayoun |first2=Bérénice A. |last3=Machado |first3=Ben |last4=Singh |first4=Param Priya |last5=Hu |first5=Chi-Kuo |last6=Pech |first6=Matthew F. |last7=Valenzano |first7=Dario Riccardo |last8=Zhang |first8=Elisa |last9=Sharp |first9=Sabrina C. |last10=Artandi |first10=Steven E. |last11=Brunet |first11=Anne |date=February 2015 |title=A Platform for Rapid Exploration of Aging and Diseases in a Naturally Short-Lived Vertebrate |journal=Cell |language=en |volume=160 |issue=5 |pages=1013–1026 |doi=10.1016/j.cell.2015.01.038|pmid=25684364 |pmc=4344913 }}</ref><ref>{{cite journal |last1=Harel |first1=Itamar |last2=Valenzano |first2=Dario Riccardo |last3=Brunet |first3=Anne |title=Efficient genome engineering approaches for the short-lived African turquoise killifish |journal=Nature Protocols |date=October 2016 |volume=11 |issue=10 |pages=2010–2028 |doi=10.1038/nprot.2016.103 |pmid=27658015 |url=https://www.nature.com/articles/nprot.2016.103 |language=en |issn=1750-2799}}</ref>, which lives only twice as long as [[Drosophila]]. By exploring [[protein aggregation]] with age, he revealed naturally occurring [[prion]]-like behaviors that propose a novel mechanism for damage propagation during aging<ref>{{cite journal |last1=Harel |first1=Itamar |last2=Chen |first2=Yiwen R. |last3=Ziv |first3=Inbal |last4=Singh |first4=Param Priya |last5=Heinzer |first5=Daniel |last6=Navarro Negredo |first6=Paloma |last7=Goshtchevsky |first7=Uri |last8=Wang |first8=Wei |last9=Astre |first9=Gwendoline |last10=Moses |first10=Eitan |last11=McKay |first11=Andrew |last12=Machado |first12=Ben E. |last13=Hebestreit |first13=Katja |last14=Yin |first14=Sifei |last15=Sánchez Alvarado |first15=Alejandro |last16=Jarosz |first16=Daniel F. |last17=Brunet |first17=Anne |title=Identification of protein aggregates in the aging vertebrate brain with prion-like and phase-separation properties |journal=Cell Reports |date=May 2024 |pages=112787 |doi=10.1016/j.celrep.2023.112787 |pmid=38810650 }}</ref><ref>{{cite journal |last1=Chen |first1=Yiwen R. |last2=Harel |first2=Itamar |last3=Singh |first3=Param Priya |last4=Ziv |first4=Inbal |last5=Moses |first5=Eitan |last6=Goshtchevsky |first6=Uri |last7=Machado |first7=Ben E. |last8=Brunet |first8=Anne |last9=Jarosz |first9=Daniel F. |title=Tissue-specific landscape of protein aggregation and quality control in an aging vertebrate |journal=Developmental Cell |date=May 2024 |doi=10.1016/j.devcel.2024.04.014 |pmid=38810654 }}</ref>. Using this emerging [[vertebrate]] model, he explores how aging is scaled between species, what mediates its [[sexual dimorphism]], and why longevity is proportional to other species-specific traits (such as age at maturity).
Harel developed a genetic platform in the naturally short-lived turquoise killifish<ref>{{Cite journal |last1=Harel |first1=Itamar |last2=Benayoun |first2=Bérénice A. |last3=Machado |first3=Ben |last4=Singh |first4=Param Priya |last5=Hu |first5=Chi-Kuo |last6=Pech |first6=Matthew F. |last7=Valenzano |first7=Dario Riccardo |last8=Zhang |first8=Elisa |last9=Sharp |first9=Sabrina C. |last10=Artandi |first10=Steven E. |last11=Brunet |first11=Anne |date=February 2015 |title=A Platform for Rapid Exploration of Aging and Diseases in a Naturally Short-Lived Vertebrate |journal=Cell |language=en |volume=160 |issue=5 |pages=1013–1026 |doi=10.1016/j.cell.2015.01.038|pmid=25684364 |pmc=4344913 }}</ref><ref>{{cite journal |last1=Harel |first1=Itamar |last2=Valenzano |first2=Dario Riccardo |last3=Brunet |first3=Anne |title=Efficient genome engineering approaches for the short-lived African turquoise killifish |journal=Nature Protocols |date=October 2016 |volume=11 |issue=10 |pages=2010–2028 |doi=10.1038/nprot.2016.103 |pmid=27658015 |url=https://www.nature.com/articles/nprot.2016.103 |language=en |issn=1750-2799}}</ref>, which lives only twice as long as [[Drosophila]]. By exploring [[protein aggregation]] with age, he revealed naturally occurring [[prion]]-like behaviors that propose an alternative mechanism for damage propagation during aging<ref>{{cite journal |last1=Harel |first1=Itamar |last2=Chen |first2=Yiwen R. |last3=Ziv |first3=Inbal |last4=Singh |first4=Param Priya |last5=Heinzer |first5=Daniel |last6=Navarro Negredo |first6=Paloma |last7=Goshtchevsky |first7=Uri |last8=Wang |first8=Wei |last9=Astre |first9=Gwendoline |last10=Moses |first10=Eitan |last11=McKay |first11=Andrew |last12=Machado |first12=Ben E. |last13=Hebestreit |first13=Katja |last14=Yin |first14=Sifei |last15=Sánchez Alvarado |first15=Alejandro |last16=Jarosz |first16=Daniel F. |last17=Brunet |first17=Anne |title=Identification of protein aggregates in the aging vertebrate brain with prion-like and phase-separation properties |journal=Cell Reports |date=May 2024 |pages=112787 |doi=10.1016/j.celrep.2023.112787 |pmid=38810650 }}</ref><ref>{{cite journal |last1=Chen |first1=Yiwen R. |last2=Harel |first2=Itamar |last3=Singh |first3=Param Priya |last4=Ziv |first4=Inbal |last5=Moses |first5=Eitan |last6=Goshtchevsky |first6=Uri |last7=Machado |first7=Ben E. |last8=Brunet |first8=Anne |last9=Jarosz |first9=Daniel F. |title=Tissue-specific landscape of protein aggregation and quality control in an aging vertebrate |journal=Developmental Cell |date=May 2024 |doi=10.1016/j.devcel.2024.04.014 |pmid=38810654 }}</ref>. Using this emerging [[vertebrate]] model, he explores how aging is scaled between species, what mediates its [[sexual dimorphism]], and why longevity is proportional to other species-specific traits (such as age at maturity).


In a series of discoveries, the Harel lab revealed novel mechanisms that regulate vertebrate longevity. They identified how [[reproduction]] might impact vertebrate aging by demonstrating that the [[germline]] itself can regulate longevity and stress resistance in a sex-specific manner.<ref name=":0" /><ref>{{Cite journal |last1=Moses |first1=Eitan |last2=Atlan |first2=Tehila |last3=Sun |first3=Xue |last4=Franěk |first4=Roman |last5=Siddiqui |first5=Atif |last6=Marinov |first6=Georgi K. |last7=Shifman |first7=Sagiv |last8=Zucker |first8=David M. |last9=Oron-Gottesman |first9=Adi |last10=Greenleaf |first10=William J. |last11=Cohen |first11=Ehud |last12=Ram |first12=Oren |last13=Harel |first13=Itamar |date=2024-05-15 |title=The killifish germline regulates longevity and somatic repair in a sex-specific manner |url=https://www.nature.com/articles/s43587-024-00632-0 |journal=Nature Aging |pages=1–23 |language=en |doi=10.1038/s43587-024-00632-0 |pmid=38750187 |issn=2662-8465}}</ref> Additionally, the Harel lab discovered a novel vertebrate longevity mechanism linked to [[energy homeostasis]] via the [[AMP-activated protein kinase]] (AMPK) pathway.<ref name=":1" /><ref>{{Cite journal |last1=Astre |first1=Gwendoline |last2=Atlan |first2=Tehila |last3=Goshtchevsky |first3=Uri |last4=Oron-Gottesman |first4=Adi |last5=Smirnov |first5=Margarita |last6=Shapira |first6=Kobi |last7=Velan |first7=Ariel |last8=Deelen |first8=Joris |last9=Levy |first9=Tomer |last10=Levanon |first10=Erez Y. |last11=Harel |first11=Itamar |date=August 2023 |title=Genetic perturbation of AMP biosynthesis extends lifespan and restores metabolic health in a naturally short-lived vertebrate |url=https://linkinghub.elsevier.com/retrieve/pii/S1534580723002484 |journal=Developmental Cell |language=en |volume=58 |issue=15 |pages=1350–1364.e10 |doi=10.1016/j.devcel.2023.05.015|pmid=37321215 }}</ref>
In a series of studies, the Harel lab revealed additional mechanisms that regulate vertebrate longevity. They identified how [[reproduction]] might impact vertebrate aging by demonstrating that the [[germline]] itself can regulate longevity and stress resistance in a sex-specific manner.<ref name=":0" /><ref>{{Cite journal |last1=Moses |first1=Eitan |last2=Atlan |first2=Tehila |last3=Sun |first3=Xue |last4=Franěk |first4=Roman |last5=Siddiqui |first5=Atif |last6=Marinov |first6=Georgi K. |last7=Shifman |first7=Sagiv |last8=Zucker |first8=David M. |last9=Oron-Gottesman |first9=Adi |last10=Greenleaf |first10=William J. |last11=Cohen |first11=Ehud |last12=Ram |first12=Oren |last13=Harel |first13=Itamar |date=2024-05-15 |title=The killifish germline regulates longevity and somatic repair in a sex-specific manner |url=https://www.nature.com/articles/s43587-024-00632-0 |journal=Nature Aging |pages=1–23 |language=en |doi=10.1038/s43587-024-00632-0 |pmid=38750187 |issn=2662-8465}}</ref> Additionally, the Harel lab discovered a novel vertebrate longevity mechanism linked to [[energy homeostasis]] via the [[AMP-activated protein kinase]] (AMPK) pathway.<ref name=":1" /><ref>{{Cite journal |last1=Astre |first1=Gwendoline |last2=Atlan |first2=Tehila |last3=Goshtchevsky |first3=Uri |last4=Oron-Gottesman |first4=Adi |last5=Smirnov |first5=Margarita |last6=Shapira |first6=Kobi |last7=Velan |first7=Ariel |last8=Deelen |first8=Joris |last9=Levy |first9=Tomer |last10=Levanon |first10=Erez Y. |last11=Harel |first11=Itamar |date=August 2023 |title=Genetic perturbation of AMP biosynthesis extends lifespan and restores metabolic health in a naturally short-lived vertebrate |url=https://linkinghub.elsevier.com/retrieve/pii/S1534580723002484 |journal=Developmental Cell |language=en |volume=58 |issue=15 |pages=1350–1364.e10 |doi=10.1016/j.devcel.2023.05.015|pmid=37321215 }}</ref>


Research in Harel's laboratory also focuses on developing advanced genetic tools, including [[Fate mapping|lineage tracing]], modeling of sporadic age-related [[Cancer|cancers]], and precise control of pituitary [[hormones]] ''in-vivo''<ref>{{cite journal |last1=Rozenberg |first1=Itai |last2=Moses |first2=Eitan |last3=Harel |first3=Itamar |title=CRISPR–Cas9 Genome Editing in Nothobranchius furzeri for Gene Knockout and Knock-In |journal=Cold Spring Harbor Protocols |date=1 February 2023 |volume=2023 |issue=2 |pages=90–99 |doi=10.1101/pdb.prot107742 |pmid=36223984 |url=https://cshprotocols.cshlp.org/content/2023/2/pdb.prot107742.short |language=en |issn=1940-3402}}</ref><ref>{{Cite journal |last1=Moses |first1=Eitan |last2=Franek |first2=Roman |last3=Harel |first3=Itamar |date=2023-10-24 |title=A scalable and tunable platform for functional interrogation of peptide hormones in fish |journal=eLife |language=en |volume=12 |doi=10.7554/eLife.85960 |doi-access=free |pmid=37872843 |pmc=10597582 |issn=2050-084X}}</ref><ref>{{Cite web |title=A new versatile tool for studying fish hormones - may transform fish farming, Eurokalert |url=https://www.eurekalert.org/news-releases/1005711}}</ref>.
Research in Harel's laboratory also focuses on developing genetic tools, including [[Fate mapping|lineage tracing]], modeling of sporadic age-related [[Cancer|cancers]], and precise control of pituitary [[hormones]] ''in-vivo''<ref>{{cite journal |last1=Rozenberg |first1=Itai |last2=Moses |first2=Eitan |last3=Harel |first3=Itamar |title=CRISPR–Cas9 Genome Editing in Nothobranchius furzeri for Gene Knockout and Knock-In |journal=Cold Spring Harbor Protocols |date=1 February 2023 |volume=2023 |issue=2 |pages=90–99 |doi=10.1101/pdb.prot107742 |pmid=36223984 |url=https://cshprotocols.cshlp.org/content/2023/2/pdb.prot107742.short |language=en |issn=1940-3402}}</ref><ref>{{Cite journal |last1=Moses |first1=Eitan |last2=Franek |first2=Roman |last3=Harel |first3=Itamar |date=2023-10-24 |title=A scalable and tunable platform for functional interrogation of peptide hormones in fish |journal=eLife |language=en |volume=12 |doi=10.7554/eLife.85960 |doi-access=free |pmid=37872843 |pmc=10597582 |issn=2050-084X}}</ref><ref>{{Cite web |title=A new versatile tool for studying fish hormones - may transform fish farming, Eurokalert |url=https://www.eurekalert.org/news-releases/1005711}}</ref>.


== Awards & Honors ==
== Awards & Honors ==

Revision as of 11:28, 2 June 2024

Itamar Harel
איתמר הראל
NationalityIsraeli
SpouseGuy Katz
Scientific career
FieldsExperimental biology of vertebrate aging and age-related diseases
InstitutionsThe Alexander Silberman Institute of Life Sciences, the Hebrew University of Jerusalem
Websitehttps://harel-lab.com/

Itamar Harel is an Israeli scientist known for his contributions to the field of Experimental Aging Research. He is faculty member in the Department of Genetics at the Alexander Silberman Institute of Life sciences, the Hebrew University of Jerusalem, Israel.

Research

Itamar Harel is a researcher in the field of biology, specifically known for his work in the areas of aging and disease (reviewed in[1][2][3][4]). Harel's research focuses on understanding the mechanisms of aging and longevity, with a particular interest in using the emerging African turquoise killifish (Nothobranchius furzeri) model to study these processes.[5][6][7][8] His work aims to uncover the biological pathways that influence aging and to develop potential interventions to promote healthy aging.

Harel developed a genetic platform in the naturally short-lived turquoise killifish[9][10], which lives only twice as long as Drosophila. By exploring protein aggregation with age, he revealed naturally occurring prion-like behaviors that propose an alternative mechanism for damage propagation during aging[11][12]. Using this emerging vertebrate model, he explores how aging is scaled between species, what mediates its sexual dimorphism, and why longevity is proportional to other species-specific traits (such as age at maturity).

In a series of studies, the Harel lab revealed additional mechanisms that regulate vertebrate longevity. They identified how reproduction might impact vertebrate aging by demonstrating that the germline itself can regulate longevity and stress resistance in a sex-specific manner.[7][13] Additionally, the Harel lab discovered a novel vertebrate longevity mechanism linked to energy homeostasis via the AMP-activated protein kinase (AMPK) pathway.[8][14]

Research in Harel's laboratory also focuses on developing genetic tools, including lineage tracing, modeling of sporadic age-related cancers, and precise control of pituitary hormones in-vivo[15][16][17].

Awards & Honors

The Harel Lab - Experimental biology of vertebrate aging and age-related diseases[20]

References

  1. ^ Marx, Vivien (January 2024). "Aging research comes of age". Nature Methods. 21 (1): 11–15. doi:10.1038/s41592-023-02140-2. ISSN 1548-7105. PMID 38167657.
  2. ^ Dance, Amber (July 2016). "Live fast, die young". Nature. 535 (7612): 453–455. Bibcode:2016Natur.535..453D. doi:10.1038/535453a. ISSN 1476-4687. PMID 27443744.
  3. ^ Singh, Param Priya; Demmitt, Brittany A.; Nath, Ravi D.; Brunet, Anne (March 2019). "The Genetics of Aging: A Vertebrate Perspective". Cell. 177 (1): 200–220. doi:10.1016/j.cell.2019.02.038. PMC 7592626. PMID 30901541.
  4. ^ Wang, Adrienne M.; Promislow, Daniel E.L.; Kaeberlein, Matt (February 2015). "Fertile Waters for Aging Research". Cell. 160 (5): 814–815. doi:10.1016/j.cell.2015.02.026. PMID 25723160.
  5. ^ Harel, Itamar (October 2022). "The turquoise killifish". Nature Methods. 19 (10): 1150–1151. doi:10.1038/s41592-022-01631-y. ISSN 1548-7091. PMID 36203025.
  6. ^ Zimmer, Carl (27 February 2015). "In Short-Lived Fish, Secrets to Aging". The New York Times.
  7. ^ a b "How germline regulation, sex differences impact the lifespan of male, female vertebrates". 15 May 2024.
  8. ^ a b "AMP biosynthesis key to longevity and metabolic health in vertebrates".
  9. ^ Harel, Itamar; Benayoun, Bérénice A.; Machado, Ben; Singh, Param Priya; Hu, Chi-Kuo; Pech, Matthew F.; Valenzano, Dario Riccardo; Zhang, Elisa; Sharp, Sabrina C.; Artandi, Steven E.; Brunet, Anne (February 2015). "A Platform for Rapid Exploration of Aging and Diseases in a Naturally Short-Lived Vertebrate". Cell. 160 (5): 1013–1026. doi:10.1016/j.cell.2015.01.038. PMC 4344913. PMID 25684364.
  10. ^ Harel, Itamar; Valenzano, Dario Riccardo; Brunet, Anne (October 2016). "Efficient genome engineering approaches for the short-lived African turquoise killifish". Nature Protocols. 11 (10): 2010–2028. doi:10.1038/nprot.2016.103. ISSN 1750-2799. PMID 27658015.
  11. ^ Harel, Itamar; Chen, Yiwen R.; Ziv, Inbal; Singh, Param Priya; Heinzer, Daniel; Navarro Negredo, Paloma; Goshtchevsky, Uri; Wang, Wei; Astre, Gwendoline; Moses, Eitan; McKay, Andrew; Machado, Ben E.; Hebestreit, Katja; Yin, Sifei; Sánchez Alvarado, Alejandro; Jarosz, Daniel F.; Brunet, Anne (May 2024). "Identification of protein aggregates in the aging vertebrate brain with prion-like and phase-separation properties". Cell Reports: 112787. doi:10.1016/j.celrep.2023.112787. PMID 38810650.
  12. ^ Chen, Yiwen R.; Harel, Itamar; Singh, Param Priya; Ziv, Inbal; Moses, Eitan; Goshtchevsky, Uri; Machado, Ben E.; Brunet, Anne; Jarosz, Daniel F. (May 2024). "Tissue-specific landscape of protein aggregation and quality control in an aging vertebrate". Developmental Cell. doi:10.1016/j.devcel.2024.04.014. PMID 38810654.
  13. ^ Moses, Eitan; Atlan, Tehila; Sun, Xue; Franěk, Roman; Siddiqui, Atif; Marinov, Georgi K.; Shifman, Sagiv; Zucker, David M.; Oron-Gottesman, Adi; Greenleaf, William J.; Cohen, Ehud; Ram, Oren; Harel, Itamar (2024-05-15). "The killifish germline regulates longevity and somatic repair in a sex-specific manner". Nature Aging: 1–23. doi:10.1038/s43587-024-00632-0. ISSN 2662-8465. PMID 38750187.
  14. ^ Astre, Gwendoline; Atlan, Tehila; Goshtchevsky, Uri; Oron-Gottesman, Adi; Smirnov, Margarita; Shapira, Kobi; Velan, Ariel; Deelen, Joris; Levy, Tomer; Levanon, Erez Y.; Harel, Itamar (August 2023). "Genetic perturbation of AMP biosynthesis extends lifespan and restores metabolic health in a naturally short-lived vertebrate". Developmental Cell. 58 (15): 1350–1364.e10. doi:10.1016/j.devcel.2023.05.015. PMID 37321215.
  15. ^ Rozenberg, Itai; Moses, Eitan; Harel, Itamar (1 February 2023). "CRISPR–Cas9 Genome Editing in Nothobranchius furzeri for Gene Knockout and Knock-In". Cold Spring Harbor Protocols. 2023 (2): 90–99. doi:10.1101/pdb.prot107742. ISSN 1940-3402. PMID 36223984.
  16. ^ Moses, Eitan; Franek, Roman; Harel, Itamar (2023-10-24). "A scalable and tunable platform for functional interrogation of peptide hormones in fish". eLife. 12. doi:10.7554/eLife.85960. ISSN 2050-084X. PMC 10597582. PMID 37872843.
  17. ^ "A new versatile tool for studying fish hormones - may transform fish farming, Eurokalert".
  18. ^ "Itamar Harel, Krill Prize 2024". 26 May 2024.
  19. ^ "Young Academy of Europe, members".
  20. ^ "The Harel Lab - Experimental biology of vertebrate aging and age-related diseases".
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