Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Efrat Laiba"'
Autor:
Salomon Israel, Elad Lerer, Idan Shalev, Florina Uzefovsky, Mathias Riebold, Efrat Laiba, Rachel Bachner-Melman, Anat Maril, Gary Bornstein, Ariel Knafo, Richard P Ebstein
Publikováno v:
PLoS ONE, Vol 4, Iss 5, p e5535 (2009)
BACKGROUND:Economic games observe social decision making in the laboratory that involves real money payoffs. Previously we have shown that allocation of funds in the Dictator Game (DG), a paradigm that illustrates costly altruistic behavior, is parti
Externí odkaz:
https://doaj.org/article/1345e585f64d4a9596d7deb1cf384c6b
Autor:
Ohad Feldstein, Salomon Israel, Efrat Laiba, David Mankuta, Ayelet Harel-Gadassi, Edwa Friedlander, Maya Yaari, Nurit Yirmiya
Publikováno v:
Autism research : official journal of the International Society for Autism Research. 12(7)
Compelling evidence for the far-reaching role of oxytocin (OT) in social cognition and affiliative behaviors set the basis for examining the association between genetic variation in the OT receptor (OXTR) gene and risk for autism spectrum disorder (A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fed143e1a2027f4bc70cf10f8d310a0e
https://pubmed.ncbi.nlm.nih.gov/31025834
https://pubmed.ncbi.nlm.nih.gov/31025834
Autor:
Klaus Pillen, Efrat Laiba, Lianne Merchuk-Ovnat, Roi Silberman, Eyal Fridman, Andreas Maurer, Adi Faigenboim
Publikováno v:
Journal of Experimental Botany
The wild barley HsDry2.2 allele confers a reproductive advantage that is independent of flowering time under drought conditions and is manifested through modifications in shoot morphology, reduced senescence, and longer grain filling.
Increasing
Increasing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::846f262fb7279679da0a3d2ea8e5d2fe
https://pubmed.ncbi.nlm.nih.gov/29365127
https://pubmed.ncbi.nlm.nih.gov/29365127
Publikováno v:
Autonomic Neuroscience. 180:59-65
Familial dysautonomia is a neurodegenerative, genetic disorder caused by an autosomal recessive mutation in the IKBKAP gene, which encodes the IkB kinase complex-associated protein. Familial dysautonomia patients have recurrent crises characterized b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00fe09b1c995efb8c1bbd977038cf273
https://doi.org/10.1016/j.autneu.2013.10.009
https://doi.org/10.1016/j.autneu.2013.10.009
Publikováno v:
Genome. 59(4)
The overdominant model of heterosis explains the superior phenotype of hybrids by synergistic allelic interaction within heterozygous loci. To map such genetic variation in yeast, we used a population doubling time dataset of Saccharomyces cerevisiae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5b13cbfadbcb8baf2ebc382491d8c8
https://pubmed.ncbi.nlm.nih.gov/26967146
https://pubmed.ncbi.nlm.nih.gov/26967146
Autor:
Ruth Shemer, Carmit Avnon Ziv, Efrat Laiba, Qing Zhou, Joel Gay, Sharona Tunovsky-Babaey, Show-Ling Shyng, Benjamin Glaser, David H. Zangen
Publikováno v:
Diabetes
Congenital hyperinsulinism (CHI) is most commonly caused by mutations in the β-cell ATP-sensitive K+ (KATP) channel genes. Severe CHI was diagnosed in a 1-day-old girl; the mother’s cousin and sister had a similar phenotype. ABCC8 gene sequencing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::357fb911ab8b6094fd91fa15548c5044
http://europepmc.org/articles/PMC3237658
http://europepmc.org/articles/PMC3237658
Autor:
Elad Lerer, Inga Gritsenko, Jacques Eisenberg, Stephen V. Faraone, Sam Tyano, Iris Manor, Efrat Laiba, Sheera Meidad, Richard P. Ebstein, Salomon Israel
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :1501-1508
The main objective of this study was to examine neuropsychological mechanisms mediating the association between tryptophan hydroxylase 2 (TPH2) and attention deficit hyperactivity disorder (ADHD). A continuous performance test (T.O.V.A.) was administ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e844635b129ef40bb350d5f12c94383a
https://doi.org/10.1002/ajmg.b.30702
https://doi.org/10.1002/ajmg.b.30702
Autor:
Yael Raz, Roi Treister, Elon Eisenberg, May Haddad, Richard P. Ebstein, Efrat Laiba, Edith Gershon, Dorit Pud
Publikováno v:
The journal of pain. 12(8)
Genetic studies have become indispensable in understanding pain mechanisms, shedding light on the role of monoamine pathways in pain modulation. The present study was aimed to explore the relationship between functional polymorphisms in serotonin and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ccb0f7d812f86628082f7f9878fd8ab
https://pubmed.ncbi.nlm.nih.gov/22564674
https://pubmed.ncbi.nlm.nih.gov/22564674
Autor:
Edith Gershon, May Haddad, Dorit Pud, Roi Treister, Elon Eisenberg, Richard P. Ebstein, Efrat Laiba
Publikováno v:
Pain. 147(1-3)
Although evidence shows that several dopamine neurotransmission pathway genes are associated with specific clinical pain syndromes, such as fibromyalgia, chronic headache, and postoperative pain, the exact role of dopamine in pain processing is not f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fdcd60e38d066c65af747c1db1cbfed
https://pubmed.ncbi.nlm.nih.gov/19796878
https://pubmed.ncbi.nlm.nih.gov/19796878
Autor:
Elad Lerer, Claudine Laurent, Efrat Laiba, Jacques Mallet, Mustafa Mujaheed, Richard P. Ebstein, Inbal Goldstein, Haim Rosen, David Lichtstein
Publikováno v:
Biological psychiatry. 65(11)
Background The sodium- and potassium-activated adenosine triphosphatase (Na + , K + -ATPase) is a major plasma membrane transporter for sodium and potassium. We recently suggested that bipolar disorders (BD) may be associated with alterations in brai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16301b1afb6da86c99e4d3aa84a1b3e7
https://pubmed.ncbi.nlm.nih.gov/19058785
https://pubmed.ncbi.nlm.nih.gov/19058785