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SPATA18 gene
Known as:
FLJ32906
, spermatogenesis associated 18
, SPERMATID-EXPRESSED GENE 1
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National Institutes of Health
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Related topics
Related topics
1 relation
SPATA16 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Gene expression changes in human iPSC-derived cardiomyocytes after X-ray irradiation
B. Becker
,
M. Majewski
,
+4 authors
R. Ullmann
International Journal of Radiation Biology
2018
Corpus ID: 52341698
Abstract Purpose: Radiation-induced heart disease caused by cardiac exposure to ionizing radiation comprises a variety of…
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2016
2016
Aging related methylation influences the gene expression of key control genes in colorectal cancer and adenoma
O. Galamb
,
A. Kalmár
,
+8 authors
B. Molnár
World Journal of Gastroenterology
2016
Corpus ID: 18303893
AIM To analyze colorectal carcinogenesis and age-related DNA methylation alterations of gene sequences associated with epigenetic…
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2015
2015
Oxidation reduction is a key process for successful treatment of psoriasis by narrow-band UVB phototherapy.
Xiaolian Gu
,
E. Nylander
,
P. Coates
,
K. Nylander
Acta Dermato-Venereologica
2015
Corpus ID: 6565034
Narrow-band UVB (NB-UVB) phototherapy is commonly used for treatment of psoriasis, though the mechanisms underlying its efficacy…
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2015
2015
Patterns of Archaic Hominin DNA in Modern Human Genomes
Benjamin Vernot
2015
Corpus ID: 88412194
from original manuscript: To reconstruct modern human evolutionary history and identify loci that have shaped huntergatherer…
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2011
2011
Identification of testis 14–3-3 binding proteins by tandem affinity purification
P. Puri
,
A. Acker-Palmer
,
Ryan Stahler
,
Yijing Chen
,
D. Kline
,
S. Vijayaraghavan
Spermatogenesis
2011
Corpus ID: 25923491
The 14–3-3 family of proteins interacts with various cellular phosphoproteins and regulates multiple cell signaling cascades…
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2005
2005
Homozygous microdeletion of chromosome 4q11‐q12 causes severe limb‐girdle muscular dystrophy type 2E with joint hyperlaxity and contractures
A. Kaindl
,
S. Jakubiczka
,
+7 authors
A. Huebner
Human Mutation
2005
Corpus ID: 33016606
Microdeletion syndromes are commonly transmitted as dominant traits and are frequently associated with variably expressed…
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