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Tabebi, Mouna
39
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Online (39)
Mediatypes
Articles (Online) (19)
OpenAccess-fulltext (20)
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1
Domain landscapes of somatic NF1 mutations in pheochromocyt..:
Tabebi, Mouna
;
Frikha, Fakher
;
Volpe, Massimiliano
..
Gene. 872 (2023) - p. 147432 , 2023
Link:
https://doi.org/10.1016/..
?
2
Novel combined UGT1A1 mutations in Crigler Najjar Syndrome ..:
Abdellaoui, Nawel
;
Abdelmoula, Balkiss
;
Abdelhedi, Rania
...
Journal of Clinical Laboratory Analysis. 36 (2022) 6 - p. , 2022
Link:
https://doi.org/10.1002/..
?
3
Loss of SDHB Induces a Metabolic Switch in the hPheo1 Cell ..:
Tabebi, Mouna
;
Kumar Dutta, Ravi
;
Skoglund, Camilla
..
International Journal of Molecular Sciences. 23 (2022) 1 - p. 560 , 2022
Link:
https://doi.org/10.3390/..
?
4
Case report: Two sisters with a germline CHEK2 variant and ..:
Vallera, Raphaelle D.
;
Ding, Yanli
;
Hatanpaa, Kimmo J.
...
Frontiers in Endocrinology. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
5
Genetic Alterations in Mitochondrial DNA Are Complementary ..:
Tabebi, Mouna
;
Łysiak, Małgorzata
;
Dutta, Ravi Kumar
...
Cancers. 14 (2022) 2 - p. 269 , 2022
Link:
https://doi.org/10.3390/..
?
6
Severe Wolfram Syndrome Caused by aNovel Frameshift Mutatio..:
Tabebi, Mouna
;
Felhi, Rahma
;
Mrabet, Houcem Elomma
...
Open Journal of Genetics. 11 (2021) 4 - p. 77-92 , 2021
Link:
https://doi.org/10.4236/..
?
7
The first concurrent detection of mitochondrial DNA m.3243A..:
Tabebi, Mouna
;
Safi, Wajdi
;
Felhi, Rahma
...
Molecular Genetics & Genomic Medicine. 8 (2020) 7 - p. , 2020
Link:
https://doi.org/10.1002/..
?
8
Potential dysfunctional effects of synonymous variants: Ins..:
Khabou, Boudour
;
Tabebi, Mouna
;
Siala‐Sahnoun, Olfa
...
Annals of Human Genetics. 82 (2018) 6 - p. 457-468 , 2018
Link:
https://doi.org/10.1111/..
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9
Association study of apoptosis gene polymorphisms in mitoch..:
Tabebi, Mouna
;
Khabou, Bodour
;
Boukadi, Hanen
...
Gene. 639 (2018) - p. 18-26 , 2018
Link:
https://doi.org/10.1016/..
?
10
First description of a novel mitochondrial mutation in the ..:
Alila-Fersi, Olfa
;
Tabebi, Mouna
;
Maalej, Marwa
...
Biochemical and Biophysical Research Communications. 497 (2018) 4 - p. 1049-1054 , 2018
Link:
https://doi.org/10.1016/..
?
11
Hypoxia Signaling and Circadian Disruption in and by Pheoch..:
Tabebi, Mouna
;
Söderkvist, Peter
;
Jensen, Lasse D.
Frontiers in Endocrinology. 9 (2018) - p. , 2018
Link:
https://doi.org/10.3389/..
?
12
A novel TBX1 missense mutation in patients with syndromic c..:
Jaouadi, Amel
;
Tabebi, Mouna
;
Abdelhedi, Fatma
...
Biochemical and Biophysical Research Communications. 499 (2018) 3 - p. 563-569 , 2018
Link:
https://doi.org/10.1016/..
?
13
Co segregation of the m.1555A>G mutation in the MT-RNR1 gen..:
Alila-Fersi, Olfa
;
Chamkha, Imen
;
Majdoub, Imen
...
Biochemical and Biophysical Research Communications. 484 (2017) 1 - p. 71-78 , 2017
Link:
https://doi.org/10.1016/..
?
14
Whole mitochondrial genome screening of a family with mater..:
Tabebi, Mouna
;
Charfi, Nadia
;
Kallabi, Fakhri
...
Journal of Diabetes and its Complications. 31 (2017) 1 - p. 253-259 , 2017
Link:
https://doi.org/10.1016/..
?
15
Phenotypic variability in a Tunisian family with X-linked a..:
Kallabi, Fakhri
;
Ellouz, Emna
;
Tabebi, Mouna
...
Clinica Chimica Acta. 453 (2016) - p. 141-146 , 2016
Link:
https://doi.org/10.1016/..
1-15