Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,475,408 papers from all fields of science
Search
Sign In
Create Free Account
CRYBA4 gene
Known as:
CRYBA4
, CRYSTALLIN, BETA-A4
, crystallin beta A4
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
CRYBA1 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Biochemical characterization of G64W mutant of acidic beta-crystallin 4.
Wenqian Li
,
Qingshan Ji
,
+15 authors
Qiwei Wang
Experimental Eye Research
2019
Corpus ID: 195762363
2019
2019
Targeted ' Next-Generation ' Sequencing in Anophthalmia and Microphthalmia Patients Confirms SOX
Nelson Lopez Jimenez
,
J. Flannick
,
+6 authors
A. Slavotinek
2019
Corpus ID: 100595083
Background: Anophthalmia/microphthalmia (A/M) is caused by mutations in several different transcription factors, but mutations in…
Expand
2018
2018
Possible association of oestrogen and Cryba4 with masticatory muscle tendon-aponeurosis hyperplasia.
N. Hayashi
,
Tsuyoshi Sato
,
+9 authors
T. Yoda
Oral Diseases
2018
Corpus ID: 5041705
OBJECTIVE Masticatory muscle tendon-aponeurosis hyperplasia, which is associated with limited mouth opening, progresses very…
Expand
2016
2016
Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts
Bushra Irum
,
S. Y. Khan
,
+15 authors
S. Riazuddin
PLoS ONE
2016
Corpus ID: 52819522
Purpose The aim of this study is to identify the molecular basis of autosomal recessive congenital cataracts (arCC) in a large…
Expand
2012
2012
Title Association of High Myopia with Crystallin Beta A 4 ( CRYBA 4 ) Gene Polymorphisms in the Linkage-Identified MYP 6 Locus
Daniel W. H. Ho
,
M. Yap
,
P. W. Ng
,
Wai Yan Fung
,
S. Yip
2012
Corpus ID: 54822365
Background: Myopia is the most common ocular disorder worldwide and imposes tremendous burden on the society. It is a complex…
Expand
Highly Cited
2011
Highly Cited
2011
Mutation analysis of 12 genes in Chinese families with congenital cataracts
Wenmin Sun
,
Xueshan Xiao
,
Shi-qiang Li
,
Xiangming Guo
,
Qingjiong Zhang
Molecular Vision
2011
Corpus ID: 2338695
Purpose To identify mutations in 12 genes in Chinese families with congenital cataracts. Methods Twenty five families with…
Expand
1995
1995
The t(II; 22)(pI5.5; qII.23) in a retroperitoneal rhabdoid tumor also includes a regional deletion distal to CRYBB2 on 22q
C. Besnard‐Guérin
,
W. Cavenee
,
Irene Newshams
1995
Corpus ID: 45516403
Translocations and deletions involving chromosomal band 22q 11 are common genetic aberrations in malignant rhabdoid tumors…
Expand
1992
1992
Localization of the beta A4-crystallin gene (CRYBA4) on human chromosome 22 in the region q11.2-->q13.1.
G. V. van Rens
,
A. G. V. Geurts van Kessel
,
H. Bloemendal
Cytogenetics and Cell Genetics
1992
Corpus ID: 46859908
The chromosomal localization of the human gene (CRYBA4) coding for the eye lens protein beta A4-crystallin has been carried out…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE
or Only Accept Required