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Tabebi, Mouna
39  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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