Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Boris, Fichtman"'
Autor:
Bar Piscon, Eliana Pia Esposito, Boris Fichtman, Guy Samburski, Lihi Efremushkin, Shimon Amselem, Amnon Harel, Galia Rahav, Raffaele Zarrilli, Ohad Gal-Mor
Publikováno v:
Microbiology Spectrum, Vol 11, Iss 3 (2023)
ABSTRACT Bacterial conjugation is one of the most abundant horizontal gene transfer (HGT) mechanisms, playing a fundamental role in prokaryote evolution. A better understanding of bacterial conjugation and its cross talk with the environment is neede
Externí odkaz:
https://doaj.org/article/503c510a6f1749879668b107c15dfd2d
Autor:
Zufit Hexner-Erlichman, Boris Fichtman, Yoav Zehavi, Morad Khayat, Haneen Jabaly-Habib, Lee S. Izhaki-Tavor, Moshe Dessau, Orly Elpeleg, Ronen Spiegel
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Cleft lip and/or cleft palate are a common group of birth defects that further classify into syndromic and non-syndromic forms. The syndromic forms are usually accompanied by additional physical or cognitive abnormalities. Isolated cleft palate syndr
Externí odkaz:
https://doaj.org/article/087cf9bd0d9e459e85e1bb186eac1b0c
Publikováno v:
Frontiers in Microbiology, Vol 12 (2021)
Clostridioides difficile is one of the leading causes of healthcare-associated diarrhea, with severity ranging from mild, self-limiting disease, to life-threatening toxic megacolon. C. difficile infection (CDI) pathogenesis is mediated by the TcdA an
Externí odkaz:
https://doaj.org/article/9c06cacfcedb45508edbea877941a8a1
Autor:
Yam Ben-Haim, Leah Armon, Boris Fichtman, Irina Epshtein, Ronen Spiegel, Amnon Harel, Achia Urbach
Publikováno v:
Stem Cell Research, Vol 56, Iss , Pp 102539- (2021)
LAP1 is an inner nuclear membrane protein encoded by TOR1AIP1. A homozygous c.961C > T loss of function mutation in TOR1AIP1 that affects both isoforms of LAP1 was recently described. This mutation leads to the development of a severe multisystemic n
Externí odkaz:
https://doaj.org/article/1df3462861af41a4802e536d62a54806
Autor:
Boris Fichtman, Fadia Zagairy, Nitzan Biran, Yiftah Barsheshet, Elena Chervinsky, Ziva Ben Neriah, Avraham Shaag, Michael Assa, Orly Elpeleg, Amnon Harel, Ronen Spiegel
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Nuclear envelopathies are a group of diseases caused by genetic mutations in essential nuclear envelope genes. Here, the authors report a nuclear envelopathy with a homozygous nonsense variant in TOR1AIP1 which leads to changes in the nuclear morphol
Externí odkaz:
https://doaj.org/article/7b3e738eaaa1487c9dd54b6c727f0181
Autor:
Einav Shemesh, Benjamin Hanf, Shelly Hagag, Shani Attias, Yana Shadkchan, Boris Fichtman, Amnon Harel, Thomas Krüger, Axel A. Brakhage, Olaf Kniemeyer, Nir Osherov
Publikováno v:
Frontiers in Microbiology, Vol 8 (2017)
Aspergillus fumigatus is the most common mold species to cause disease in immunocompromised patients. Infection usually begins when its spores (conidia) are inhaled into the airways, where they germinate, forming hyphae that penetrate and destroy the
Externí odkaz:
https://doaj.org/article/cefcedf1cfac47b1825bcec4dc15bc98
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2502
Field emission scanning electron microscopy (FESEM) is a well-established technique for acquiring three-dimensional surface images of nuclear pore complexes (NPCs). We present an optimized protocol for the exposure of mammalian cell nuclei and direct
Autor:
Amani Daoud, Boris Fichtman, Netanel Eisenbach, Eyal Zussman, Offir Ertracht, Amnon Harel, Forsan Jahshan, Aiman Abu Ammar, Eyal Sela, Shaul Atar, Maayan Gruber
Publikováno v:
ACS applied bio materials. 4(5)
upper airway complications are common sequelae of endotracheal tube (ETT) intubation, and systemic corticosteroids are considered a mainstay treatment for this problem. Drug-eluting ETT may present an attractive option for topical steroid delivery wh
Publikováno v:
Methods in Molecular Biology ISBN: 9781071623367
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47beb8644174a892c40504f180e9e193
https://doi.org/10.1007/978-1-0716-2337-4_29
https://doi.org/10.1007/978-1-0716-2337-4_29
Autor:
Michael Assa, Fadia Zagairy, Ronen Spiegel, Orly Elpeleg, Ziva Ben Neriah, Nitzan Biran, Amnon Harel, Boris Fichtman, Avraham Shaag, Elena Chervinsky, Yiftah Barsheshet
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Nature Communications
Nature Communications
Nuclear envelopathies comprise a heterogeneous group of diseases caused by mutations in genes encoding nuclear envelope proteins. Mutations affecting lamina-associated polypeptide 1 (LAP1) result in two discrete phenotypes of muscular dystrophy and p