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1. 
Generation and characterization of three dimensional organotypic KID syndrome skin model için kapak resmi
Generation and characterization of three dimensional organotypic KID syndrome skin model
Generation and characterization of three dimensional organotypic KID syndrome skin model
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Öztürk, Özgür, author.
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blot and qRT-PCR analysis confirmed Cx26 expression in stable cell lines, meaning these cell lines can
2. 
Deciphering functions of aberrant hemichannels formed by connexin 26- 130N and D50Y mutations için kapak resmi
Deciphering functions of aberrant hemichannels formed by connexin 26- 130N and D50Y mutations
Deciphering functions of aberrant hemichannels formed by connexin 26- 130N and D50Y mutations
by 
Aypek, Hande, author.
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connexin isoform and mutations on the Cx26 gene (GJB2) cause non-syndromic and syndromic deafness
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