» Authors » Sarah M Kamel

Sarah M Kamel

Explore the profile of Sarah M Kamel including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 12
Citations 295
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Kamel S, Daroczi L, Toth L, Beke D, Juarez G, Cobo S, et al.
J Mater Chem C Mater . 2024 Apr; 12(16):5757-5765. PMID: 38680543
Acoustic emission from the compounds [Fe(HB(tz))] and [Fe(Htrz)(trz)]BF was detected during the thermally induced spin transition and is correlated with simultaneously recorded calorimetric signals. We ascribe this phenomenon to elastic...
2.
Kahanamoku-Meyer S, Samuels-Fair M, Kamel S, Stewart D, Wu B, Kahn L, et al.
Sci Data . 2024 Jan; 11(1):144. PMID: 38291058
The Santa Barbara Basin is an extraordinary archive of environmental and ecological change, where varved sediments preserve microfossils that provide an annual to decadal record of the dynamics of surrounding...
3.
Beke D, Kamel S, Daroczi L, Toth L
Materials (Basel) . 2022 Dec; 15(24). PMID: 36556816
In some shape-memory single crystals the stress-strain (~) curves, belonging to stress induced martensitic transformations from austenite to martensite at fixed temperature, instead of being the usual slightly increasing function...
4.
Kamel S, Samy N, Toth L, Daroczi L, Beke D
Materials (Basel) . 2022 Jul; 15(13). PMID: 35806681
There are many systems producing crackling noise (avalanches) in materials. Temporal shapes of avalanches, () ( is the detected voltage signal, is the time), have self-similar behaviour and the normalized...
5.
Solman M, Blokzijl-Franke S, Piques F, Yan C, Yang Q, Strullu M, et al.
Elife . 2022 May; 11. PMID: 35535491
Gain-of-function mutations in the protein-tyrosine phosphatase SHP2 are the most frequently occurring mutations in sporadic juvenile myelomonocytic leukemia (JMML) and JMML-like myeloproliferative neoplasm (MPN) associated with Noonan syndrome (NS). Hematopoietic...
6.
Kamel S, Broekman S, Tessadori F, van Wijk E, Bakkers J
Dev Dyn . 2022 Mar; 251(8):1357-1367. PMID: 35275424
Background: Cohesinopathies is a term that refers to/covers rare genetic diseases caused by mutations in the cohesin complex proteins. The cohesin complex is a multiprotein complex that facilitates different aspects...
7.
Kamel S, Koopman C, Kruse F, Willekers S, Chocron S, Bakkers J
J Cardiovasc Dev Dis . 2021 Apr; 8(4). PMID: 33924051
Cardiomyopathies are a group of heterogeneous diseases that affect the muscles of the heart, leading to early morbidity and mortality in young and adults. Genetic forms of cardiomyopathy are caused...
8.
Dona M, Waaijers S, Richter S, Eisenhofer G, Korving J, Kamel S, et al.
Endocr Relat Cancer . 2020 Nov; 28(1):65-77. PMID: 33156815
Pheochromocytomas and paragangliomas (PPGLs) caused by mutations in the B-subunit of the succinate dehydrogenase (SDHB) have the highest metastatic rate among PPGLs, and effective systemic therapy is lacking. To unravel...
9.
Smeland M, McClenaghan C, Roessler H, Savelberg S, Hansen G, Hjellnes H, et al.
Nat Commun . 2019 Oct; 10(1):4457. PMID: 31575858
Mutations in genes encoding K channel subunits have been reported for pancreatic disorders and Cantú syndrome. Here, we report a syndrome in six patients from two families with a consistent...
10.
Sommer F, Torraca V, Kamel S, Lombardi A, Meijer A
J Leukoc Biol . 2019 Sep; 107(2):185-203. PMID: 31529512
The CXCR3-CXCL11 chemokine-signaling axis plays an essential role in infection and inflammation by orchestrating leukocyte trafficking in human and animal models, including zebrafish. Atypical chemokine receptors (ACKRs) play a fundamental...