Miraoui, Hichem
26  results:
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3

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Ide..:

Miraoui, Hichem ; Dwyer, Andrew A. ; Sykiotis, Gerasimos P....
The American Journal of Human Genetics.  92 (2013)  5 - p. 725-743 , 2013
 
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4

Role of fibroblast growth factor (FGF) signaling in the neu..:

Miraoui, Hichem ; Dwyer, Andrew ; Pitteloud, Nelly
Molecular and Cellular Endocrinology.  346 (2011)  1-2 - p. 37-43 , 2011
 
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8

Molecular silencing of Twist1 enhances osteogenic different..:

Miraoui, Hichem ; Severe, Nicolas ; Vaudin, Pascal..
Journal of Cellular Biochemistry.  110 (2010)  5 - p. 1147-1154 , 2010
 
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10

Fibroblast Growth Factor Receptor 2 Promotes Osteogenic Dif..:

Miraoui, Hichem ; Oudina, Karim ; Petite, Hervé...
Journal of Biological Chemistry.  284 (2009)  8 - p. 4897-4904 , 2009
 
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11

KLB , encoding β‐Klotho, is mutated in patients with congen..:

Xu, Cheng ; Messina, Andrea ; Somm, Emmanuel...
https://eprints.hud.ac.uk/id/eprint/32532/1/Xu%20Messina%20Kinnunen%20et%20al%20EMBO%20Mol%20Med%202017.pdf.  , 2017
 
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12

KLB , encoding β‐Klotho, is mutated in patients with congen..:

Xu, Cheng ; Messina, Andrea ; Somm, Emmanuel...
info:eu-repo/semantics/altIdentifier/doi/10.15252/emmm.201607376.  , 2017
 
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13

KLB, encoding β-Klotho, is mutated in patients with congeni..:

Xu, Cheng ; Messina, Andrea ; Somm, Emmanuel...
info:eu-repo/semantics/altIdentifier/doi/10.15252/emmm.201607376.  , 2017
 
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14

KLB , encoding β‐Klotho, is mutated in patients with congen..:

Xu, Cheng ; Messina, Andrea ; Somm, Emmanuel...
info:eu-repo/semantics/altIdentifier/doi/10.15252/emmm.201607376.  , 2017
 
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15

KLB, encoding β‐Klotho, is mutated in patients with congeni..:

Xu, Cheng ; Messina, Andrea ; Somm, Emmanuel...
Xu , C , Messina , A , Somm , E , Miraoui , H , Kinnunen , T , Acierno , J , Niederländer , N J , Bouilly , J , Dwyer , A A , Sidis , Y , Cassatella , D , Sykiotis , G P , Quinton , R , De Geyter , C , Dirlewanger , M , Schwitzgebel , V , Cole , T R , Toogood , A A , Kirk , J M , Plummer , L , Albrecht , U , Crowley , W F , Mohammadi , M , Tena‐sempere , M , Prevot , V & Pitteloud , N 2017 , ' KLB, encoding β‐Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism ' , EMBO Molecular Medicine , vol. 9 , no. 10 , pp. 1379-1397 . https://doi.org/10.15252/emmm.201607376.  , 2017
 
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