[HTML][HTML] An evolutionarily conserved mechanism for microRNA-223 expression revealed by microRNA gene profiling

T Fukao, Y Fukuda, K Kiga, J Sharif, K Hino, Y Enomoto… - Cell, 2007 - cell.com
Many microRNAs (miRNAs) are evolutionarily conserved and have intriguing expression
patterns. Tissue and/or time-specific expressions of some miRNAs are presumably …

Mutations for Gaucher disease confer high susceptibility to Parkinson disease

J Mitsui, I Mizuta, A Toyoda, R Ashida… - Archives of …, 2009 - jamanetwork.com
Background Increased frequency of pathogenic variants inGBA, the causative gene for
Gaucher disease, has been suggested to be associated with Parkinson disease (PD) …

[PDF][PDF] ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19

Y Takahashi, Y Fukuda, J Yoshimura, A Toyoda… - The American Journal of …, 2013 - cell.com
Amyotrophic lateral sclerosis (ALS) is a devastating neurological disorder characterized by
the degeneration of motor neurons and typically results in death within 3–5 years from onset …

[HTML][HTML] Global terrestrial carbon fluxes of 1999–2019 estimated by upscaling eddy covariance data with a random forest

J Zeng, T Matsunaga, ZH Tan, N Saigusa, T Shirai… - Scientific data, 2020 - nature.com
The terrestrial biosphere is a key player in slowing the accumulation of carbon dioxide in the
atmosphere. While quantification of carbon fluxes at global land scale is important for …

[PDF][PDF] Dominant mutations in RP1L1 are responsible for occult macular dystrophy

M Akahori, K Tsunoda, Y Miyake, Y Fukuda… - The American Journal of …, 2010 - cell.com
Occult macular dystrophy (OMD) is an inherited macular dystrophy characterized by
progressive loss of macular function but normal ophthalmoscopic appearance. Typical OMD …

Management of refractory Mycoplasma pneumoniae pneumonia: utility of measuring serum lactate dehydrogenase level

N Inamura, N Miyashita, S Hasegawa, A Kato… - Journal of Infection and …, 2014 - Elsevier
It has been suggested that cytokines are associated with refractory Mycoplasma
pneumoniae pneumonia, and steroid administration is reported to be effective in this …

Impact of MET inhibitors on survival among patients with non-small cell lung cancer harboring MET exon 14 mutations: a retrospective analysis

MM Awad, GC Leonardi, S Kravets, SE Dahlberg… - Lung Cancer, 2019 - Elsevier
Objectives Although dramatic responses to MET inhibitors have been reported in patients
with MET exon 14 (METex14) mutant non-small cell lung cancer (NSCLC), the impact of …

[HTML][HTML] Macrolide-resistant Mycoplasma pneumoniae infection, Japan, 2008–2015

T Tanaka, T Oishi, I Miyata, S Wakabayashi… - Emerging infectious …, 2017 - ncbi.nlm.nih.gov
We evaluated isolates obtained from children with Mycoplasma pneumoniae infection
throughout Japan during 2008–2015. The highest prevalence of macrolide-resistant M …

A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)

H Shimazaki, Y Takiyama, H Ishiura, C Sakai… - Journal of medical …, 2012 - jmg.bmj.com
Background Autosomal recessive hereditary spastic paraplegias (AR-HSP) constitute a
heterogeneous group of neurodegenerative diseases involving pyramidal tracts dysfunction …

[PDF][PDF] Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation

H Doi, K Yoshida, T Yasuda, M Fukuda… - The American Journal of …, 2011 - cell.com
Autosomal-recessive cerebellar ataxias (ARCAs) are clinically and genetically
heterogeneous disorders associated with diverse neurological and nonneurological …