Review of carbon capture absorbents for CO2 utilization
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 …
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
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 …
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
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 …
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) …
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 …
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 …
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
Sporosarcina pasteurii is a well-known ureolytic microbial species that proficiently induces
the deposition of calcium carbonate through microbially induced carbonate precipitation …
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 …
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 …
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 …
aspartate/glutamate carrier isoform 2 (AGC2), and SLC25A13 mutations cause citrin …