Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2018 1
2019 1
2020 1
2021 5
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

9 results

Results by year

Filters applied: . Clear all
Page 1
UBA1 Variations in Neutrophilic Dermatosis Skin Lesions of Patients With VEXAS Syndrome.
Zakine E, Schell B, Battistella M, Vignon-Pennamen MD, Chasset F, Mahévas T, Cordoliani F, Adès L, Sébert M, Delaleu J, Jachiet M, Lepelletier C, Lemaire P, Chauvel C, Dhouaieb B, Kim R, Cassius C, Georgin-Lavialle S, Mekinian A, Bagot M, Braun T, Rousset L, Begon E, de Masson A, Fenaux P, Clappier E, Bouaziz JD. Zakine E, et al. Among authors: schell b. JAMA Dermatol. 2021 Nov 1;157(11):1349-1354. doi: 10.1001/jamadermatol.2021.3344. JAMA Dermatol. 2021. PMID: 34495287 Free PMC article.
Myelodysplastic Syndrome associated TET2 mutations affect NK cell function and genome methylation.
Boy M, Bisio V, Zhao LP, Guidez F, Schell B, Lereclus E, Henry G, Villemonteix J, Rodrigues-Lima F, Gagne K, Retiere C, Larcher L, Kim R, Clappier E, Sebert M, Mekinian A, Fain O, Caignard A, Espeli M, Balabanian K, Toubert A, Fenaux P, Ades L, Dulphy N. Boy M, et al. Among authors: schell b. Nat Commun. 2023 Feb 3;14(1):588. doi: 10.1038/s41467-023-36193-w. Nat Commun. 2023. PMID: 36737440 Free PMC article.
[Abstracts of the 4th CoBioMe Congress].
Brousseau J, Bastide M, Cadenet M, Caillault A, Ducastel M, Étienne ML, Filser M, François A, Guemas E, Guilbert Z, Jatteau P, Lodin M, Ouaziz K, Rouabah L, Sakhi S, Schell B, Puel M, Roche M. Brousseau J, et al. Among authors: schell b. Ann Biol Clin (Paris). 2021 Jun 25:265-275. doi: 10.1684/abc.2021.1649. Online ahead of print. Ann Biol Clin (Paris). 2021. PMID: 34170254 French. No abstract available.
[First edition of the CoBioMe congress].
Michel M, Le Guillou E, Schell B, Janot C. Michel M, et al. Among authors: schell b. Ann Biol Clin (Paris). 2018 Apr 1;76(2):205-216. doi: 10.1684/abc.2018.1341. Ann Biol Clin (Paris). 2018. PMID: 29623891 Free article. French. No abstract available.
EPHA7 haploinsufficiency is associated with a neurodevelopmental disorder.
Lévy J, Schell B, Nasser H, Rachid M, Ruaud L, Couque N, Callier P, Faivre L, Marle N, Engwerda A, van Ravenswaaij-Arts CMA, Plutino M, Karmous-Benailly H, Benech C, Redon S, Boute O, Boudry Labis E, Rama M, Kuentz P, Assoumani J, Maldergem LV, Dupont C, Verloes A, Tabet AC. Lévy J, et al. Among authors: schell b. Clin Genet. 2021 Oct;100(4):396-404. doi: 10.1111/cge.14017. Epub 2021 Jul 1. Clin Genet. 2021. PMID: 34176129
[Second edition of the CoBioMe congress].
Janot C, Lefrère B, Michel M, Le Guillou E, Schell B. Janot C, et al. Among authors: schell b. Ann Biol Clin (Paris). 2019 Apr 1;77(2):233-240. doi: 10.1684/abc.2019.1435. Ann Biol Clin (Paris). 2019. PMID: 30998203 Free article. French. No abstract available.
Prevalence of UBA1 mutations in MDS/CMML patients with systemic inflammatory and auto-immune disease.
Zhao LP, Schell B, Sébert M, Kim R, Lemaire P, Boy M, Mathis S, Larcher L, Chauvel C, Dhouaieb MB, Bisio V, Preudhomme C, Marceau-Renaut A, Itzykson R, Mekinian A, Fain O, Toubert A, Fenaux P, Dulphy N, Clappier E, Adès L. Zhao LP, et al. Among authors: schell b. Leukemia. 2021 Sep;35(9):2731-2733. doi: 10.1038/s41375-021-01353-8. Epub 2021 Aug 3. Leukemia. 2021. PMID: 34344988 No abstract available.