Ons Mamai
Overview
Explore the profile of Ons Mamai including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
330
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0
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Recent Articles
1.
Chen S, Mamai O, Akhurst R
Annu Rev Cancer Biol
. 2022 Nov;
6(1):123-146.
PMID: 36382146
Discovered over four decades ago, transforming growth factor β (TGFβ) is a potent pleiotropic cytokine that has context-dependent effects on most cell types. It acts as a tumor suppressor in...
2.
Mamai O, Dodagatta-Marri E, Akhurst R
Biotarget
. 2019 Mar;
2.
PMID: 30906919
No abstract available.
3.
Budi E, Mamai O, Hoffman S, Akhurst R, Derynck R
iScience
. 2019 Jan;
11:474-491.
PMID: 30684493
Angiogenesis, the development of new blood vessels, is a key process in disease. We reported that insulin promotes translocation of transforming growth factor β (TGF-β) receptors to the plasma membrane...
4.
Chourabi M, Liew M, Lim S, Hmida-Ben Brahim D, Boussofara L, Dai L, et al.
J Invest Dermatol
. 2017 Oct;
138(2):291-300.
PMID: 28964717
Cole disease is a genodermatosis of pigmentation following a strict dominant mode of inheritance. In this study, we investigated eight patients affected with an overlapping genodermatosis after recessive inheritance. The...
5.
Zhong F, Mamai O, Sborgi L, Boussofara L, Hopkins R, Robinson K, et al.
Cell
. 2016 Sep;
167(1):187-202.e17.
PMID: 27662089
Inflammasome complexes function as key innate immune effectors that trigger inflammation in response to pathogen- and danger-associated signals. Here, we report that germline mutations in the inflammasome sensor NLRP1 cause...
6.
Ben Charfeddine I, Ben Lazreg T, Ben Rayana N, Amara A, Mamai O, Knani L, et al.
Ann Biol Clin (Paris)
. 2015 Sep;
73(4):469-73.
PMID: 26411914
Choroideremia is a rare X-linked recessive, hereditary retinal pigment epithelial dystrophy, characterized by night blindness and progressive constriction of the visual fields leading to blindness in young adulthood. In this...
7.
Ghedir H, Gribaa M, Mamai O, Ben Charfeddine I, Braham A, Amara A, et al.
J Assist Reprod Genet
. 2015 Sep;
32(11):1651-8.
PMID: 26341096
Purpose: Macrozoospermia is a rare condition of male infertility characterized by the presence of close to 100 % large-headed multiflagellar spermatozoa. The homozygous mutation (c.144delC) in aurora kinase C gene...
8.
Amara A, Ben Charfeddine I, Ghedir H, Mamai O, Jemni-Yacoub S, Chaieb L, et al.
Iran J Public Health
. 2015 Apr;
44(3):396-403.
PMID: 25905084
Background: HNF4A-p.I463Vvariant, reported previously in two distinct families suspected of MODY-1, is assessed in this report to determine whether it is a mutation or a polymorphism (frequency >1%). Methods: 200...
9.
Mamai O, Boussofara L, Denguezli M, Escande-Beillard N, Kraeim W, Merriman B, et al.
J Invest Dermatol
. 2014 Jul;
135(1):304-308.
PMID: 25050600
No abstract available.
10.
Pohler E, Mamai O, Hirst J, Zamiri M, Horn H, Nomura T, et al.
Nat Genet
. 2012 Oct;
44(11):1272-6.
PMID: 23064416
Palmoplantar keratodermas (PPKs) are a group of disorders that are diagnostically and therapeutically problematic in dermatogenetics. Punctate PPKs are characterized by circumscribed hyperkeratotic lesions on the palms and soles with...