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2. 
The effects of calcium on NF-KB pathway in hacat cells containing connexin26 kid syndrome mutations için kapak resmi
The effects of calcium on NF-KB pathway in hacat cells containing connexin26 kid syndrome mutations
The effects of calcium on NF-KB pathway in hacat cells containing connexin26 kid syndrome mutations
by 
Yaşarbaş, Sümeyye Şüheda, author.
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Keratitis-ichthyosis-deafness (KID) syndrome is a rare genetic disorder characterized by deafness
3. 
Characterization of connexin 26 mutations causing hereditary skin disorders için kapak resmi
Characterization of connexin 26 mutations causing hereditary skin disorders
Characterization of connexin 26 mutations causing hereditary skin disorders
by 
Bay, Veysel.
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skin disorders. One of them is a rare congenital skin disorder; Keratitis- Ichthyosis-Deafness (KID
4. 
Investigating the function of CX26I30N and D50Y mutations in soquamous cell carcinoma cell line SCC-25 için kapak resmi
Investigating the function of CX26I30N and D50Y mutations in soquamous cell carcinoma cell line SCC-25
Investigating the function of CX26I30N and D50Y mutations in soquamous cell carcinoma cell line SCC-25
by 
Yavuz, Büşra, author.
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diseases. For example, more than 10 missense mutations in the Cx26 gene cause keratitis-ichthyosis
5. 
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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. Keratitis-ichthyosis-deafness (KID) syndrome is one of the syndromic deafness disorders caused by Cx26 mutations. Among these
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