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Search Results - Hakim, Bochra
Search Results - Hakim, Bochra
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Evaluation of the Combinatory Anticancer Effect of Chemotherapeutic Compounds and Prodigiosin against HCT-116, LoVo, and A549 Cell lines
by
Elghali, Fares
,
Msalbi, Dhouha
,
Frikha, Fakher
,
Alonazi, Mona
,
Sahli, Emna
,
Hakim, Bochra
,
Mnif, Sami
,
Ben Bacha, Abir
,
Aifa, Sami
Published in
ACS omega
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Chemical alternative for cell identification and cross-contamination detection
by
Msalbi, Dhouha
,
Elloumi-Mseddi, Jihene
,
Hakim, Bochra
,
Sahli, Emna
,
Aifa, Sami
Published in
3 Biotech
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Toxicity evaluation of synthetic glucocorticoids against breast cancer cell lines MDA-MB-231, MCF-7 and human embryonic kidney HEK293
by
Msalbi, Dhouha
,
Jellali, Fatma
,
Elloumi-Mseddi, Jihene
,
Hakim, Bochra
,
Sahli, Emna
,
Aifa, Sami
Published in
Medical oncology (Northwood, London, England)
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Selective cytotoxicity of arene tricarbonylchromium towards tumour cell lines
by
Elloumi-Mseddi, Jihene
,
Mnif, Sami
,
Akacha, Nejmeddine
,
Hakim, Bochra
,
Pigeon, Pascal
,
Jaouen, Gérard
,
Top, Siden
,
Aifa, Sami
Published in
Journal of organometallic chemistry
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Controversial effect on Erk activation of some cytotoxic drugs in human LOVO colon cancer cells
by
Jemel-Oualha, Ikram
,
Elloumi-Mseddi, Jihene
,
Beji, Abdelhamid
,
Hakim, Bochra
,
Aifa, Sami
Published in
Journal of receptors and signal transduction
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Effect of estradiol and clomiphene citrate on Erk activation in breast cancer cells
by
Elloumi-Mseddi, Jihene
,
Jemel-Oualha, Ikram
,
Beji, Abdelhamid
,
Hakim, Bochra
,
Aifa, Sami
Published in
Journal of receptors and signal transduction
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A novel dominant mutation in SIX1 , affecting a highly conserved residue, result in only auditory defects in humans
by
Mosrati, Mohamed Ali
,
Hammami, Boutheina
,
Rebeh, Imen Ben
,
Ayadi, Leila
,
Dhouib, Leila
,
Ben mahfoudh, Khaireddine
,
Hakim, Bochra
,
Charfeddine, Ilhem
,
Mnif, Jameleddine
,
Ghorbel, Abdelmonem
,
Masmoudi, Saber
Published in
European journal of medical genetics
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Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population
by
Khalfallah, Ayda
,
Schrauwen, Isabelle
,
Mnejja, Malek
,
HadjKacem, Hassen
,
Dhouib, Leila
,
Mosrati, Mohamed Ali
,
Hakim, Bochra
,
Lahmar, Imed
,
Charfeddine, Ilhem
,
Driss, Nabil
,
Ayadi, Hammadi
,
Ghorbel, Abdelmonem
,
Van Camp, Guy
,
Masmoudi, Saber
Published in
Annals of human genetics
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A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family
by
Ben Saïd, Mariem
,
Ayedi, Leila
,
Mnejja, Melek
,
Hakim, Bochra
,
Khalfallah, Ayda
,
Charfeddine, Ilhem
,
Khifagi, Chamseddine
,
Turki, Khalil
,
Ayadi, Hammadi
,
BenZina, Zeineb
,
Ghorbel, Abdelmonem
,
Castillo, Ignacio del
,
Masmoudi, Saber
,
Aifa, Mounira Hmani
Published in
European journal of medical genetics
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DFNB66 and DFNB67 loci are non allelic and rarely contribute to autosomal recessive nonsyndromic hearing loss
by
Bensaïd, Mariem
,
Hmani-Aifa, Mounira
,
Hammami, Boutheina
,
Tlili, Abdelaziz
,
Hakim, Bochra
,
Charfeddine, Ilhem
,
Ayadi, Hammadi
,
Ghorbel, Abdelmonem
,
Castillo, Ignacio del
,
Masmoudi, Saber
Published in
European journal of medical genetics
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Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population: COL1A1 & TGFB1 variants and otosclerosis
by
Khalfallah, Ayda
,
Schrauwen, Isabelle
,
Mnejja, Malek
,
HadjKacem, Hassen
,
Dhouib, Leila
,
Mosrati, Mohamed Ali
,
Hakim, Bochra
,
Lahmar, Imed
,
Charfeddine, Ilhem
,
Driss, Nabil
,
Ayadi, Hammadi
,
Ghorbel, Abdelmonem
,
Van Camp, Guy
,
Masmoudi, Saber
Published in
Annals of human genetics
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Identification of candidate regions for a novel Usher syndrome type II locus
by
Ben Rebeh, Imen
,
Benzina, Zeineb
,
Dhouib, Houria
,
Hadjamor, Imen
,
Amyere, Mustapha
,
Ayadi, Leila
,
Turki, Khalil
,
Hammami, Bouthaina
,
Kmiha, Noureddine
,
Kammoun, Hassen
,
Hakim, Bochra
,
Charfedine, Ilhem
,
Vikkula, Miikka
,
Ghorbel, Abdelmonem
,
Ayadi, Hammadi
,
Masmoudi, Saber
Published in
Molecular vision
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