Huiyan Huang

ORCID: 0000-0003-1239-7191
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About
Contact & Profiles
Research Areas
  • Genetics, Aging, and Longevity in Model Organisms
  • Circadian rhythm and melatonin
  • Mitochondrial Function and Pathology
  • Spaceflight effects on biology
  • ATP Synthase and ATPases Research
  • Metabolism and Genetic Disorders
  • Photosynthetic Processes and Mechanisms
  • Autism Spectrum Disorder Research
  • Obsessive-Compulsive Spectrum Disorders
  • Lipid Membrane Structure and Behavior
  • Advanced MRI Techniques and Applications
  • Pancreatic function and diabetes
  • Pluripotent Stem Cells Research
  • 3D Printing in Biomedical Research
  • Cellular transport and secretion
  • Yeasts and Rust Fungi Studies
  • Acute Myeloid Leukemia Research
  • Ion channel regulation and function
  • Nuclear Structure and Function
  • Body Image and Dysmorphia Studies
  • Hemoglobin structure and function
  • Autophagy in Disease and Therapy
  • Neonatal Respiratory Health Research
  • Epigenetics and DNA Methylation
  • Transcranial Magnetic Stimulation Studies

The First People's Hospital of Guiyang
2025

Guangdong General Hospital
2015-2024

Washington University in St. Louis
1992-2023

Pediatrics and Genetics
2023

St. Louis Children's Hospital
2019

Brown University
2013-2018

Guangdong Academy of Medical Sciences
2015-2018

Allen Institute for Brain Science
2018

University of South Florida
2016

South China University of Technology
2015

GLUT-4 is the major facilitative glucose transporter isoform in tissues that exhibit insulin-stimulated transport. Insulin regulates transport by rapid translocation of from an intracellular compartment to plasma membrane. A critical feature this process efficient exclusion membrane absence insulin. To identify amino acid domains which confer sequestration, we analyzed subcellular distribution chimeric transporters comprised and a homologous isoform, GLUT-1, found predominantly at cell...

10.1083/jcb.117.4.729 article EN The Journal of Cell Biology 1992-05-15

Background:Cognitive impairment is a key feature of treatment-resistant depression (TRD) and can be related to the anterior cingulate cortex (ACC) function. Repetitive transcranial magnetic stimulation (rTMS) as an antidepressant intervention has increasingly been investigated in last two decades. However, no studies date have association between neurobiochemical changes within executive dysfunction measured TRD being treated with rTMS.

10.1093/ijnp/pyv059 article EN cc-by-nc The International Journal of Neuropsychopharmacology 2015-05-29

Lipins are phosphatidic acid phosphatases with a pivotal role in regulation of triglyceride and glycerophospholipid metabolism. Lipin1 is also an amplifier PGC-1α, nuclear coactivator PPAR-α responsive gene transcription. do not contain recognized membrane-association domains, but interaction these enzymes cellular membranes necessary for access to their phospholipid substrate. We identified conserved polybasic amino motif N-terminal domain previously implicated as determinant localization...

10.1091/mbc.e10-01-0073 article EN Molecular Biology of the Cell 2010-07-22

Stem cell systems are essential for the development and maintenance of polarized tissues. Intercellular signaling pathways control stem systems, where niche cells signal to maintain fate/self-renewal inhibit differentiation. In C. elegans germline, GLP-1 Notch specifies fate, employing sequence-specific DNA binding protein LAG-1 implement transcriptional response. We undertook a comprehensive genome-wide approach identify targets signaling. expected primary response target genes be evident...

10.1371/journal.pgen.1008650 article EN cc-by PLoS Genetics 2020-03-20

Significance The Rab5 GTPase functions in early endosome (EE) fusion the endocytic pathway. Here, we propose that RAB5B also has a noncanonical vesicular function regulated secretion pathway produces mature surfactant proteins SP-B and SP-C lung. This was revealed from investigation of proband with interstitial lung disease suggestive dysfunction disorder who carried de novo Asp136His variant gene. Our modeling C. elegans provided information on genetic cell biological mechanism, analyses...

10.1073/pnas.2105228119 article EN cc-by Proceedings of the National Academy of Sciences 2022-02-04

Aims/Background Patients with relapsed acute myeloid leukemia (AML) have a poor prognosis and limited treatment options. The combination of azacitidine venetoclax has demonstrated some efficacy in AML. This study aimed to investigate the effects combined on immune function quality life patients Methods retrospectively analyzed clinical data 104 AML who were admitted First People's Hospital Fuyang from January 2020 2024. divided into group (n = 53, treated azacitidine) an 51, according...

10.12968/hmed.2024.0416 article EN cc-by-nc British Journal of Hospital Medicine 2025-03-05

Mitochondria are highly dynamic organelles whose morphology and position within the cell is tightly coupled to metabolic function. There a limited list of essential proteins that regulate mitochondrial mechanisms govern dynamics poorly understood. However, recent evidence indicates core machinery governs linked complex intracellular signalling cascades, including apoptotic pathways, cycle transitions nuclear factor kappa B activation. Given emerging importance plasticity in pathways...

10.1186/1741-7007-8-100 article EN cc-by BMC Biology 2010-07-26

Sleep deprivation impairs learning, causes stress, and can lead to death. Notch JNK-1 pathways impact C. elegans sleep in complex ways; these have been hypothesized involve compensatory sleep. DAF-16, a FoxO transcription factor, is required for homeostatic response decreased DAF-16 loss decreases survival after bout deprivation. Here, we investigate connections between the requirement mechanical stress. Reduced function of ligand LAG-2 or kinase resulted increased time bouts during...

10.1186/s12868-018-0408-1 article EN cc-by BMC Neuroscience 2018-03-09

Abstract Sleep is evolutionarily conserved and required for organism homeostasis survival. Despite this importance, the molecular cellular mechanisms underlying sleep are not well understood. Caenorhabditis elegans exhibits sleep-like behavioral quiescence thus provides a valuable, simple model system study of regulators process. In C. elegans, epidermal growth factor receptor (EGFR) signaling in neurosecretory neuron ALA to promote after stress. We describe novel role VAV-1, guanine...

10.1534/genetics.115.183038 article EN Genetics 2016-01-21

C. elegans sleep during development is regulated by genes and cellular mechanisms that are conserved across the animal kingdom (Singh et al., 2014; Trojanowski & Raizen, 2016). developmental usually assessed transition to adulthood, a 2.6 h time interval called lethargus (Raizen 2008; Singh 2011). During lethargus, animals cycle between periods of immobility (sleep bouts) active locomotion (motion bouts). Sleep bouts resemble in other species based on behavioral criteria, including cessation...

10.21769/bioprotoc.2174 article EN BIO-PROTOCOL 2017-01-01

We aimed to test a combined approach identify conserved genes regulating sleep and explore the association between DNA methylation length. identified candidate associated with shorter versus longer duration in college students based on using Illumina Infinium HumanMethylation450 BeadChip arrays. Orthologous Caenorhabditis elegans were identified, we examined whether their loss of function affected C. sleep. For whose perturbation sleep, subsequently undertook small pilot study re-examine an...

10.1093/sleep/zsx063 article EN SLEEP 2017-04-18

In Caenorhabditis elegans, Notch signaling regulates developmentally timed sleep during the transition from L4 larval stage to adulthood (L4/A) . To identify core pathways and find genes acting downstream of signaling, we undertook first genome-wide, classical genetic screen focused on C. elegans sleep. increase efficiency, looked for mutations that suppressed inappropriate anachronistic in adult hsp::osm-11 animals overexpressing coligand OSM-11 after heat shock. We retained suppressor...

10.1534/g3.117.300071 article EN cc-by G3 Genes Genomes Genetics 2017-07-26

Abstract The molecular mechanisms of sleep are not fully understood. Huang et al. demonstrate that loss Caenorhabditis elegans UNC-7 or UNC-9 innexins dramatically reduces during L4/A lethargus and those partially required... An essential characteristic is heightened arousal threshold, with decreased behavioral response to external stimuli. cellular underlying threshold changes We report innexin function reduced developmentally timed in elegans. was required premotor interneurons motor...

10.1534/genetics.118.301551 article EN Genetics 2018-10-15

Due to its ease of genetic manipulation and transparency, Caenorhabditis elegans (C. elegans) has become a preferred model system study gene function by microscopy. The use Aequorea victoria green fluorescent protein (GFP) fused proteins or targeting sequences interest, further expanded upon the utility C. labeling subcellular structures, which enables following their disposition during development in presence mutations. Fluorescent with excitation emission spectra different from that GFP...

10.1371/journal.pone.0214257 article EN cc-by PLoS ONE 2019-03-26

Standards-based COTS (common-off-the-shelf) middleware has been shown to be effective in meeting a range of functional and QoS (quality service) requirements for distributed real-time embedded (DRE) systems. Each standard makes limiting assumptions, often implicit, about the fundamental set system capabilities constraints typical domain which applies. When characteristics particular class systems violates standard's it may appropriate modify or extent its conforming implementations better...

10.1109/words.2003.1218080 article EN 2003-10-31
Klaas Koop Weimin Yuan Federico Tessadori Wilmer R. Rodriguez-Polanco Jeremy J. Grubbs and 95 more Bo Zhang Matt Osmond Gail E. Graham Sarah L. Sawyer Erin Conboy Francesco Vetrini Kayla Treat Rafał Płoski Victor Murcia Pienkowski Anna Kłosowska Elizabeth L. Fieg Joel B. Krier Coralie Mallebranche Alban Ziegler Kimberly A. Aldinger Deborah Ritter Ellen F. Macnamara Bonnie Sullivan John Herriges Joseph T. Alaimo Catherine Helbig Colin A. Ellis Clare L. van Eyk Jozef Gécz Daniel J. Farrugia Ikeoluwa Osei‐Owusu Lesley C. Adès Marie-José van den Boogaard Sabine A. Fuchs Jeroen Bakker Karen Duran Zachary Dawson Anika Lindsey Huiyan Huang Dustin Baldridge Gary A. Silverman Barth D. Grant David M. Raizen Maria T. Acosta Margaret P Adam David R. Adams Justin Alvey Laura M. Amendola Ashley Andrews Euan A. Ashley Mahshid S. Azamian Carlos A. Bacino Güney Bademci Ashok Balasubramanyam Dustin Baldridge Jim Bale Michael Bamshad Deborah Barbouth Pinar Bayrak‐Toydemir Anita Beck Alan H. Beggs Edward M. Behrens Gill Bejerano Hugo J. Bellen Jimmy Bennet Beverly Berg-Rood Jonathan A. Bernstein Gerard T. Berry Anna Bican Stephanie Bivona Elizabeth Blue John Bohnsack Devon Bonner Lorenzo D. Botto Brenna Boyd Lauren C. Briere Elly Brokamp Gabrielle Brown Elizabeth A. Burke Lindsay C. Burrage Manish J. Butte Peter H. Byers William E. Byrd John C. Carey Olveen Carrasquillo Thomas Cassini Ta Chen Chang Sirisak Chanprasert Hsiao‐Tuan Chao Gary Clark Terra R. Coakley Laurel A. Cobban Joy D. Cogan Matthew Coggins F. Sessions Cole Heather A. Colley Cynthia M. Cooper Heidi Cope William J. Craigen Andrew B. Crouse

Abstract Rab GTPases are important regulators of intracellular vesicular trafficking. RAB5C is a member the GTPase family that plays an role in endocytic pathway, membrane protein recycling and signaling. Here we report on 12 individuals with nine different heterozygous de novo variants RAB5C. All but one patient missense (n = 9) exhibited macrocephaly, combined mild-to-moderate developmental delay. Patients loss function 2) had apparently more severe clinical phenotype refractory epilepsy...

10.1093/hmg/ddad130 article EN cc-by-nc Human Molecular Genetics 2023-08-08
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