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GJB4 gene
Known as:
CX30.3
, GJB4
, gap junction protein beta 4
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National Institutes of Health
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Related topics
Related topics
2 relations
GJB3 gene
GJB5 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana
S. M. Adadey
,
K. Esoh
,
O. Quaye
,
G. Amedofu
,
G. Awandare
,
A. Wonkam
Experimental biology and medicine
2020
Corpus ID: 219588564
The contribution of GJB4 and GJC3 gene variants to hearing impairment in Africa has not yet been studied. Here, we investigated…
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2017
2017
Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss…
Masoud Akbarzadeh Laleh
,
Marzieh Naseri
,
+5 authors
A. Nejatizadeh
Journal of Research in Medical Sciences
2017
Corpus ID: 8061067
Background: We aimed to determine the contribution of four DFNB loci and mutation analysis of gap junction beta-2 (GJB2) and GJB4…
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2017
2017
Régulation de l'expression des connexines dans la différenciation de l'épithélium épididymaire
C. Adam
2017
Corpus ID: 192795965
L’epididyme est l’organe responsable de la maturation des spermatozoides, son role est essentiel dans l’acquisition de la…
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2016
2016
Japanese sporadic case of erythrokeratodermia variabilis caused by the connexin‐30.3 (GJB4) mutation: Is Glycine 12 a mutational hotspot in the connexin family?
Yumie Yoshikata-Isokawa
,
M. Itoh
,
H. Nakagawa
Journal of dermatology (Print)
2016
Corpus ID: 21960087
was treated with a recombinant growth hormone until adolescence, which resulted in her reaching the height of 153 cm. Until she…
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2016
2016
ANALYSIS OF BLOOD TRANSCRIPTOME IN PATIENTS WITH CHRONIC KIDNEY DISEASE OF UNCERTAIN AETIOLOGY
Saravanabavan Sayanthooran
,
D. Magana-Arachchi
,
L. Gunarathne
,
T. Abeysekera
,
S. Sooriyapathirana
2016
Corpus ID: 55887920
Chronic kidney disease of uncertain aetiology (CKDu) is an increasing health problem in certain agricultural regions of the…
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2015
2015
Association between mutations in the gap junction β4 gene and nonsyndromic hearing loss: genotype-phenotype correlation patterns.
Tung-Cheng Li
,
Wen‐Hung Wang
,
Chuan Li
,
Jiann-Jou Yang
Molecular Medicine Reports
2015
Corpus ID: 23314913
Numerous studies have confirmed that gap junctions, composed of connexin (Cx) protein, are essential for auditory function…
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2013
2013
بررسی وراثت دوژنی ژن GJB4 در ناشنوایان غیرسندرومی مغلوب اتوزومی دارای یک آلل جهشیافته GJB2
دنیز کوشاور
,
عفت فرخی
,
مرضیه ابولحسنی
,
فر محمدامینطباطبایی
,
محمدرضا نوری دلویی
,
مرتضی هاشم زاده چالشتری
2013
Corpus ID: 178055069
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