Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 222,883,786 papers from all fields of science
Search
Sign In
Create Free Account
LETM1 gene
Known as:
Mdm38 homolog (yeast)
, LETM1
, LEUCINE ZIPPER/EF-HAND-CONTAINING TRANSMEMBRANE PROTEIN 1
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
2 relations
LETM2 gene
LETMD1 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Natural histories of patients with Wolf‐Hirschhorn syndrome derived from variable chromosomal abnormalities
Keiko Yamamoto-Shimojima
,
Masanori Kouwaki
,
+6 authors
Toshiyuki Yamamoto
Congenital Anomalies
2018
Corpus ID: 53107779
Wolf‐Hirschhorn syndrome (WHS) is a subtelomeric deletion syndrome affecting the short arm of chromosome 4. The main clinical…
Expand
Review
2016
Review
2016
Exploring the developmental mechanisms underlying Wolf-Hirschhorn Syndrome: Evidence for defects in neural crest cell migration
Erin L. Rutherford
,
L. A. Lowery
Developmental Biology
2016
Corpus ID: 18252695
2016
2016
Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with…
Wen-Xu Yang
,
H. Pan
,
Song-tao Wang
,
Lin Li
,
Hai-rong Wu
,
Y. Qi
Taiwanese Journal of Obstetrics & Gynecology
2016
Corpus ID: 27602994
2016
2016
Coupling of LETM1 up-regulation with oxidative phosphorylation and platelet-derived growth factor receptor signaling via YAP1 transactivation
Jandee Lee
,
Woo Kyung Lee
,
+8 authors
Y. Jo
OncoTarget
2016
Corpus ID: 9262227
Persistent cellular proliferation and metabolic reprogramming are essential processes in carcinogenesis. Here, we performed Gene…
Expand
2015
2015
A zebrafish model of Letm 1 and Letm 2 deficiency verfasst
Von
,
S. Hajny
2015
Corpus ID: 102338599
Page 81 6. Abstract Wolf Hirschhorn Syndrome (WHS) is severe gene deletion syndrome associated with a wide range of related…
Expand
2014
2014
Elevated mRNA-levels of distinct mitochondrial and plasma membrane Ca2+ transporters in individual hypoglossal motor neurons of endstage SOD1 transgenic mice
T. Mühling
,
J. Duda
,
Jochen H Weishaupt
,
A. Ludolph
,
B. Liss
Frontiers in Cellular Neuroscience
2014
Corpus ID: 17374505
Disturbances in Ca2+ homeostasis and mitochondrial dysfunction have emerged as major pathogenic features in familial and sporadic…
Expand
2014
2014
Wolf-Hirschhorn Syndrome with Buphthalmos
Rugmini Kamalammal
,
L. Subha
,
S. Rao
2014
Corpus ID: 54038323
Wolf-Hirschhorn syndrome is a 4p-deletion syndrome in which there is reduced growth, abnormal phenotype, developmental delay…
Expand
2014
2014
Antiporter + / H 2 + Genome-Wide RNAi Screen Identifies Letm 1 as a Mitochondrial Ca
S. Blandin
,
R. Wang-Sattler
,
+4 authors
L. Steinmetz
2014
Corpus ID: 207768355
, 144 (2009); 326 Science et al. Dawei Jiang Antiporter + /H 2+ Genome-Wide RNAi Screen Identifies Letm1 as a Mitochondrial Ca…
Expand
2013
2013
for Mitochondrial Potassium Homeostasis Trypanosome Letm 1 Protein Is Essential Bioenergetics :
J. Lukeš
,
H. Hashimi
,
L. McDonald
,
Éva
2013
Corpus ID: 207790347
2011
2011
Subcellular tissue proteomics of hepatocellular carcinoma for molecular signature discovery.
Yong-yook Lee
,
Kimberly Q. McKinney
,
+9 authors
Sun-il Hwang
Journal of Proteome Research
2011
Corpus ID: 19993930
Hepatocellular carcinoma (HCC) is one of the leading causes of mortality from solid organ malignancy worldwide. Because of the…
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