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SMAD6 gene
Known as:
MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 6
, SMAD, Mothers Against DPP Homolog 6 (Drosophila) Gene
, SMAD6
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This gene is involved in signal transduction and regulation of transcription. It also plays a role in development.
National Institutes of Health
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Related topics
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3 relations
SMAD6 protein, human
Signal Transduction
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SMAD6 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Genetic testing for aortic valve stenosis
Y. Rakhmanov
,
P. Maltese
,
+4 authors
M. Bertelli
The EuroBiotech Journal
2018
Corpus ID: 80854023
Abstract Aortic valve stenosis (AVS) is a congenital aortic defect in which the aortic lumen narrows due to thickening or…
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2017
2017
The Transcriptional Network Structure of a Myeloid Cell: A Computational Approach
J. Espinal-Enríquez
,
Daniel González-Terán
,
E. Hernández-Lemus
International Journal of Genomics
2017
Corpus ID: 2798162
Understanding the general principles underlying genetic regulation in eukaryotes is an incomplete and challenging endeavor. The…
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2017
2017
The TGF-β Family Accessory Type III Receptor Function in Cancer Progression
G. Sherbet
2017
Corpus ID: 89783063
2017
2017
RESULTS MANTIS Is a JARID 1 B-Suppressed lncRNA Downregulated in Human Idiopathic Pulmonary Arterial Hypertension
M. Leisegang
2017
Corpus ID: 30728819
2011
2011
Comparison of gene expression profiles of human dental pulp cells treated with mineral trioxide aggregate and calcium hydroxide
Yong-Beom Kim
,
W. Shon
,
Woocheol Lee
,
K. Kum
,
S. Baek
,
K. Bae
2011
Corpus ID: 96165838
Kim YB, DDS, MSD, PhD, Program in Conservative Dentistry, Seoul National University Graduate School,
2011
2011
Mad for SMAD: unraveling the genetics of a new aneurysm syndrome
S. Ladha
Clinical Genetics
2011
Corpus ID: 21213031
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early‐onset osteoarthritis
Review
2011
Review
2011
132 Non-synonymous SMAD6 mutations impaired inhibition of bmp signalling in patients with congenital cardiovascular malformation
H. Tan
,
E. Glen
,
+10 authors
B. Keavney
Heart
2011
Corpus ID: 72714635
Introduction Congenital cardiovascular malformation (CVM) exhibits familial predisposition but the specific genetic factors…
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2008
2008
[Smad7 instead of Smad6 blocks epithelial-mesenchymal transition induced by TGF-beta in human renal proximal tubule epithelial cells].
Yunjian Huang
,
Zihua Wang
,
Jingbo Zhang
,
Li Liang
,
Feng Chen
,
Jing-hong Zhao
Xi bao yu fen zi mian yi xue za zhi = Chinese…
2008
Corpus ID: 22940519
AIM To investigate whether Smad6 and Smad7 can regulate TGF-beta-induced epithelial-mesenchymal transition in human renal…
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2006
2006
A Genome-wide Scan Maps a Novel Juvenile-Onset Primary Open-Angle Glaucoma Locus to 15 q
Dan-yi Wang
,
B. Fan
,
+4 authors
C. Pang
2006
Corpus ID: 28680717
METHODS. A complete ophthalmic examination was conducted, and genomic DNA was obtained from 25 members of a Chinese family, of…
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2001
2001
The N domain of Smad 7 is essential for specific inhibition of transforming growth factor-signaling
A. Hanyu
,
Y. Ishidou
,
Takanori Ebisawa
,
T. Shimanuki
,
T. Imamura
,
K. Miyazono
2001
Corpus ID: 13383222
nhibitory Smads (I-Smads) repress signaling by cytokines of the transforming growth factor(TGF) superfamily. I-Smads have…
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