OpenAlex 3.057 eser 52 yazar konusu
Çalışmalar
3.057 eser
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %1
OpenAlex 100.0%
BACKGROUND: Spinal muscular atrophy is an autosomal recessive neuromuscular disorder that is caused by an insufficient level of survival motor neuron (SMN) protein. Nusinersen is an antisense oligonucleotide drug that modifies pre-messenger RNA splicing of the SMN2 gene and thus promotes increased production of full-l…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %1
OpenAlex 100.0%
BACKGROUND: Spinal muscular atrophy is an autosomal recessive neuromuscular disorder that is caused by an insufficient level of survival motor neuron (SMN) protein. Nusinersen is an antisense oligonucleotide drug that modifies pre-messenger RNA splicing of the SMN2 gene and thus promotes increased production of full-l…
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YÖKSİS
SJR Q3
JCR Q4
OpenAlex üst %10
OpenAlex 97.8%
Cranioplasty is the surgical intervention to repair cranial defects. The aim of cranioplasty is not only a cosmetic issue; also, the repair of cranial defects gives relief to psychological drawbacks and increases the social performances. Many different types of materials were used throughout the history of cranioplast…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %1
OpenAlex 99.6%
Orofacial clefts (OFCs), which include non-syndromic cleft lip with or without cleft palate (CL/P), are among the most common birth defects in humans, affecting approximately 1 in 700 newborns.CL/P is phenotypically heterogeneous and has a complex etiology caused by genetic and environmental factors.Previous genome-wi…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %1
OpenAlex 99.6%
Orofacial clefts (OFCs), which include non-syndromic cleft lip with or without cleft palate (CL/P), are among the most common birth defects in humans, affecting approximately 1 in 700 newborns. CL/P is phenotypically heterogeneous and has a complex etiology caused by genetic and environmental factors. Previous genome-…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex 68.9%
Özet henüz yok.
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %1
OpenAlex 99.3%
Mandibulofacial dysostosis with microcephaly (MFDM) is a rare sporadic syndrome comprising craniofacial malformations, microcephaly, developmental delay, and a recognizable dysmorphic appearance. Major sequelae, including choanal atresia, sensorineural hearing loss, and cleft palate, each occur in a significant propor…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %1
OpenAlex 99.3%
Mandibulofacial dysostosis with microcephaly (MFDM) is a rare sporadic syndrome comprising craniofacial malformations, microcephaly, developmental delay, and a recognizable dysmorphic appearance. Major sequelae, including choanal atresia, sensorineural hearing loss, and cleft palate, each occur in a significant propor…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %10
OpenAlex 96.0%
Özet henüz yok.
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %10
OpenAlex 95.8%
Özet henüz yok.
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Mutation of PVRL1 is Associated with Sporadic Non syndromic Cleft Lip Palate in Northern Venezuela 2001YÖKSİS OpenAlex üst %10 OpenAlex 97.1%
Özet henüz yok.
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex üst %1
OpenAlex 99.3%
Özet henüz yok.
Akademisyenler
52 akademisyen
- İBRAHİM SİNA UÇKAN 42 yazar konusu
- REHA ŞÜKRÜ KİŞNİŞCİ 30 yazar konusu
- DOĞAN DOLANMAZ 29 yazar konusu
- ALTAN VAROL 21 yazar konusu
- SELÇUK BASA 21 yazar konusu
- GÖKMEN KURT 14 yazar konusu
- ZEKERİYA TOSUN 14 yazar konusu
- YAVUZ FINDIK 13 yazar konusu
- AYŞE NURTEN AKARSU 11 yazar konusu
- DERYA ÇAKAN 11 yazar konusu
- FUNDA AKSU 9 yazar konusu
- MUSTAFA CİHAT AVUNDUK 9 yazar konusu