Review of carbon capture absorbents for CO2 utilization

SYW Chai, LH Ngu, BS How - Greenhouse Gases: Science and …, 2022 - Wiley Online Library
Carbon capture technologies have been recognized as a potential alternative to alleviate
global warming. Carbon capture and storage (CCS) is preferred over carbon conversion and …

A review of CO2 adsorbents performance for different carbon capture technology processes conditions

JY Lai, LH Ngu, SS Hashim - Greenhouse Gases: Science and …, 2021 - Wiley Online Library
The utilization of various conventional and emerging solid adsorbents is an attractive carbon
capture method for post‐combustion and direct air capture (DAC). This review aims to …

Hydrogen sulfide (H2S) conversion to hydrogen (H2) and value-added chemicals: Progress, challenges and outlook

YH Chan, ACM Loy, KW Cheah, SYW Chai… - Chemical Engineering …, 2023 - Elsevier
Hydrogen sulfide (H 2 S) is a toxic gas released from natural occurrences (such as
volcanoes, hot springs, municipal waste decomposition) and human economic activities …

Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency

L Brun, LH Ngu, WT Keng, GS Ch'Ng, YS Choy… - Neurology, 2010 - AAN Enterprises
Objective: To describe the current treatment; clinical, biochemical, and molecular findings;
and clinical follow-up of patients with aromatic l-amino acid decarboxylase (AADC) …

[PDF][PDF] OFD1 is mutated in X-linked Joubert syndrome and interacts with LCA5-encoded lebercilin

KLM Coene, R Roepman, D Doherty, B Afroze… - The American Journal of …, 2009 - cell.com
We ascertained a multi-generation Malaysian family with Joubert syndrome (JS). The
presence of asymptomatic obligate carrier females suggested an X-linked recessive …

Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene

MS Ebberink, B Csanyi, WK Chong, S Denis… - Journal of medical …, 2010 - jmg.bmj.com
Background Zellweger syndrome spectrum disorders are caused by mutations in any of at
least 12 different PEX genes. This includes PEX16, which encodes an integral peroxisomal …

Low-cost cultivation of Sporosarcina pasteurii strain in food-grade yeast extract medium for microbially induced carbonate precipitation (MICP) application

AI Omoregie, LH Ngu, DEL Ong, PM Nissom - Biocatalysis and Agricultural …, 2019 - Elsevier
Sporosarcina pasteurii is a well-known ureolytic microbial species that proficiently induces
the deposition of calcium carbonate through microbially induced carbonate precipitation …

[HTML][HTML] Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes

N Himmelreich, M Bertoldi, M Alfadhel… - Molecular genetics and …, 2023 - Elsevier
Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare autosomal recessive
genetic disorder affecting the biosynthesis of dopamine, a precursor of both norepinephrine …

Progressive deafness–dystonia due to SERAC1 mutations: A study of 67 cases

RR Maas, K Iwanicka‐Pronicka… - Annals of …, 2017 - Wiley Online Library
Objective 3‐Methylglutaconic aciduria, dystonia–deafness, hepatopathy, encephalopathy,
Leigh‐like syndrome (MEGDHEL) syndrome is caused by biallelic variants in SERAC1 …

[HTML][HTML] SLC25A13 Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in …

YZ Song, ZH Zhang, WX Lin, XJ Zhao, M Deng… - PLoS …, 2013 - journals.plos.org
Background The human SLC25A13 gene encodes citrin, the liver-type mitochondrial
aspartate/glutamate carrier isoform 2 (AGC2), and SLC25A13 mutations cause citrin …