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Select item 116998361.

First Report from Saudi Arabia of Trimethylaminuria Caused by a Premature Stop Codon Mutation in the FMO3 Gene

Bandar Alghanem, Hassan S Alamri, Tlili Barhoumi, Imran Ali Khan, Khawlah Almuhalhil, Essra Aloyouni, Hayat Shaibah, Abdullah Mashhour, Shatha Algheribe, Imadul Islam, Mohamed Boudjelal, Majid Alfadhel

Appl Clin Genet. 2024; 17: 215–228. Published online 2024 Dec 31. doi: 10.2147/TACG.S497959

PMCID:: PMC11699836

Article PDF–7.2M

Select item 107979232.

Living with trimethylaminuria and body and breath malodour: personal perspectives

Cole C. Flaherty, Ian R. Phillips, Azara Janmohamed, Elizabeth A. Shephard

BMC Public Health. 2024; 24: 222. Published online 2024 Jan 18. doi: 10.1186/s12889-024-17685-w

PMCID:: PMC10797923

Article PDF–954K

Select item 96676753.

FMO3 deficiency of duck leads to decreased lipid deposition and increased antibacterial activity

Xingzheng Li, Jianlou Song, Xuefeng Shi, Mingyi Huang, Lei Liu, Guoqiang Yi, Ning Yang, Guiyun Xu, Jiangxia Zheng

J Anim Sci Biotechnol. 2022; 13: 119. Published online 2022 Nov 16. doi: 10.1186/s40104-022-00777-1

PMCID:: PMC9667675

Article PDF–4.4M

Select item 95511844.

Altered gut microbiota and gut-derived p-cresyl sulfate serum levels in peritoneal dialysis patients

Manchen Bao, Pan Zhang, Shulan Guo, Jianzhou Zou, Jun Ji, Xiaoqiang Ding, Xiaofang Yu

Front Cell Infect Microbiol. 2022; 12: 639624. Published online 2022 Sep 27. doi: 10.3389/fcimb.2022.639624

PMCID:: PMC9551184

Article PDF–6.4M

Select item 94077135.

TMAO Suppresses Megalin Expression and Albumin Uptake in Human Proximal Tubular Cells Via PI3K and ERK Signaling

Stefania Kapetanaki, Ashok Kumar Kumawat, Katarina Persson, Isak Demirel

Int J Mol Sci. 2022 Aug; 23(16): 8856. Published online 2022 Aug 9. doi: 10.3390/ijms23168856

PMCID:: PMC9407713

Article PDF–4.9M

Select item 89580536.

Endovascular Treatment of Congenital Portosystemic Shunt: A Single-Center Prospective Study

María-Dolores Ponce-Dorrego, Teresa Hernández-Cabrero, Gonzalo Garzón-Moll

Pediatr Gastroenterol Hepatol Nutr. 2022 Mar; 25(2): 147–162. Published online 2022 Mar 10. doi: 10.5223/pghn.2022.25.2.147

PMCID:: PMC8958053

Article PDF–3.0M

Select item 86187687.

Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes

Simona Alibrandi, Fabiana Nicita, Luigi Donato, Concetta Scimone, Carmela Rinaldi, Rosalia D’Angelo, Antonina Sidoti

Molecules. 2021 Nov; 26(22): 7045. Published online 2021 Nov 22. doi: 10.3390/molecules26227045

PMCID:: PMC8618768

Article PDF–3.6M

Select item 84378658.

The use of an in-vitro batch fermentation (human colon) model for investigating mechanisms of TMA production from choline, l-carnitine and related precursors by the human gut microbiota

Priscilla Day-Walsh, Emad Shehata, Shikha Saha, George M. Savva, Barbora Nemeckova, Jasmine Speranza, Lee Kellingray, Arjan Narbad, Paul A. Kroon

Eur J Nutr. 2021; 60(7): 3987–3999. Published online 2021 May 2. doi: 10.1007/s00394-021-02572-6

PMCID:: PMC8437865

Article PDF–1.1M

Select item 79120989.

Gut-Brain Axis Cross-Talk and Limbic Disorders as Biological Basis of Secondary TMAU

Luigi Donato, Simona Alibrandi, Concetta Scimone, Andrea Castagnetti, Giacomo Rao, Antonina Sidoti, Rosalia D’Angelo

J Pers Med. 2021 Feb; 11(2): 87. Published online 2021 Jan 31. doi: 10.3390/jpm11020087

PMCID:: PMC7912098

Article PDF–3.5M

Select item 780365710.

Le Carbone prevents liver damage in non-alcoholic steatohepatitis-hepatocellular carcinoma mouse model via AMPKα-SIRT1 signaling pathway activation

Mst. Rejina Afrin, Somasundaram Arumugam, Vigneshwaran Pitchaimani, Vengadeshprabhu Karuppagounder, Rajarajan Amirthalingam Thandavarayan, Meilei Harima, Chowdhury Faiz Hossain, Kenji Suzuki, Hirohito Sone, Yasuhiro Matsubayashi, Kenichi Watanabe

Heliyon. 2021 Jan; 7(1): e05888. Published online 2021 Jan 5. doi: 10.1016/j.heliyon.2020.e05888

PMCID:: PMC7803657

Article PDF–1.6M

Select item 780262111.

Impact of trimethylaminuria on daily psychosocial functioning

Daniel Roddy, Philomena McCarthy, Darragh Nerney, Jennifer Mulligan‐Rabbitt, Edwin Smith, Eileen P. Treacy

JIMD Rep. 2021 Jan; 57(1): 67–75. Published online 2020 Oct 6. doi: 10.1002/jmd2.12170

PMCID:: PMC7802621

Article PDF–1.0M

Select item 733402412.

TMAO, a seafood-derived molecule, produces diuresis and reduces mortality in heart failure rats

Marta Gawrys-Kopczynska, Marek Konop, Klaudia Maksymiuk, Katarzyna Kraszewska, Ladislav Derzsi, Krzysztof Sozanski, Robert Holyst, Marta Pilz, Emilia Samborowska, Leszek Dobrowolski, Kinga Jaworska, Izabella Mogilnicka, Marcin Ufnal

eLife. 2020; 9: e57028. Published online 2020 Jun 8. doi: 10.7554/eLife.57028

PMCID:: PMC7334024

Article PDF–6.6M

Select item 717526113.

Engineered Polymersomes for the Treatment of Fish Odor Syndrome: A First Randomized Double Blind Olfactory Study

Aaron C. Schmidt, Erik R. Hebels, Charlotte Weitzel, Anna Kletzmayr, Yinyin Bao, Christian Steuer, Jean‐Christophe Leroux

Adv Sci (Weinh) 2020 Apr; 7(8): 1903697. Published online 2020 Mar 9. doi: 10.1002/advs.201903697

PMCID:: PMC7175261

Article PDF–1.2M

Select item 705732314.

Fabrication of Biobased Hydrophobic Hybrid Cotton Fabrics Using Molecular Self-Assembly: Applications in the Development of Gas Sensor Fabrics

Ayyapillai Thamizhanban, Guru Prasanth Sarvepalli, Krishnamoorthy Lalitha, Yadavali Siva Prasad, Dinesh Kumar Subbiah, Apurba Das, John Bosco Balaguru Rayappan, Subbiah Nagarajan

ACS Omega. 2020 Mar 3; 5(8): 3839–3848. Published online 2020 Feb 12. doi: 10.1021/acsomega.9b02733

PMCID:: PMC7057323

Article PDF–9.4M

Select item 685650915.

Endovascular Closure Resolves Trimethylaminuria Caused by Congenital Portosystemic Shunts

María Dolores Ponce-Dorrego, Gonzalo Garzón-Moll

Pediatr Gastroenterol Hepatol Nutr. 2019 Nov; 22(6): 588–593. Published online 2019 Nov 7. doi: 10.5223/pghn.2019.22.6.588

PMCID:: PMC6856509

Article PDF–893K

Select item 675187516.

Diagnosis and phenotypic assessment of trimethylaminuria, and its treatment with riboflavin: ¹H NMR spectroscopy and genetic testing

Nadia Bouchemal, Lisa Ouss, Anaïs Brassier, Valérie Barbier, Stéphanie Gobin, Laurence Hubert, Pascale de Lonlay, Laurence Le Moyec

Orphanet J Rare Dis. 2019; 14: 222. Published online 2019 Sep 18. doi: 10.1186/s13023-019-1174-6

PMCID:: PMC6751875

Article PDF–469K

Select item 673686817.

NMR-based newborn urine screening for optimized detection of inherited errors of metabolism

Nieves Embade, Claire Cannet, Tammo Diercks, Rubén Gil-Redondo, Chiara Bruzzone, Sara Ansó, Lourdes Román Echevarría, M. Mercedes Martinez Ayucar, Laura Collazos, Blanca Lodoso, Eneritz Guerra, Izaskun Asla Elorriaga, Miguel Ángel Kortajarena, Alberto Pérez Legorburu, Fang Fang, Itziar Astigarraga, Hartmut Schäfer, Manfred Spraul, Oscar Millet

Sci Rep. 2019; 9: 13067. Published online 2019 Sep 10. doi: 10.1038/s41598-019-49685-x