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Search life-sciences literature (45,104,145 articles, preprints and more)

Suggested authors matching "AUTH:Tlili A" with an ORCID

Anis Tlili
CNRS Délégation Rhône-Auvergne
33
Publications
488
Citations
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Abdelaziz Tlili
University of Sharjah
28
Publications
527
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1-25 of 187 results

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Identification of Genes Associated with Familial Focal Segmental Glomerulosclerosis Through Transcriptomics and In Silico Analysis, Including RPL27, TUBB6, and PFDN5.
Mahmoud AH, Alhamidi RS, Ilce BY, Hamad AM, Ali N, Mahasneh A, Talaat IM, Tlili A, Hamoudi R
Int J Mol Sci, 25(21):11659, 30 Oct 2024
Cited by: 0 articles | PMID: 39519211 | PMCID: PMC11546068
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Impact of missense mutations on the structure-function relationship of human succinyl-CoA synthetase using in silico analysis.
Elabed S, Alila Fersi O, Tlili A, Fendri A, Fakhfakh F
Mitochondrion, 80:101978, 03 Nov 2024
Cited by: 0 articles | PMID: 39500468
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Photochemically Driven Palladium- Phosphinoacridine Catalysis: A Carboxylative Approach for Arylcarbamate Synthesis.
Tang R, Yang Y, Abid S, Amgoune A, Tlili A
ChemSusChem, e202401958, 17 Oct 2024
Cited by: 0 articles | PMID: 39417206
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Formate Salt as a Bifunctional Reagent for Hydroxylation and Carbonylation Reactions Under Photochemically Driven Nickel Catalysis.
Yang Y, Su J, Guerin T, Nielsen M, Tlili A
Chemistry, e202403221, 31 Aug 2024
Cited by: 0 articles | PMID: 39215548
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Congenital anomalies of the kidney and urinary tract.
Mahmoud AH, Talaat IM, Tlili A, Hamoudi R
Front Med (Lausanne), 11:1384676, 15 Jul 2024
Cited by: 0 articles | PMID: 39076761 | PMCID: PMC11284074
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This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
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Genetic analysis of 106 sporadic cases with hearing loss in the UAE population.
Tlili A, Mahfood M, Al Mutery A, Chouchen J
Hum Genomics, 18(1):59, 07 Jun 2024
Cited by: 0 articles | PMID: 38844983
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How do Chinese and Egyptian science textbooks differ? A cross-country comparative research.
Metwally AHS, Tlili A, Wang Y, Li Z, Zhao J, Shehata B, Yang D, Huang R
Heliyon, 10(12):e32380, 05 Jun 2024
Cited by: 0 articles | PMID: 39183839 | PMCID: PMC11341347
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Designing a Simple Electrochemical Genosensor for the Detection of Urinary PCA3, a Prostate Cancer Biomarker.
Mokni M, Tlili A, Khalij Y, Attia G, Zerrouki C, Hmida W, Othmane A, Bouslama A, Omezzine A, Fourati N
Micromachines (Basel), 15(5):602, 29 Apr 2024
Cited by: 0 articles | PMID: 38793175 | PMCID: PMC11123437
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The Segregation of p.Arg68Ter-CLDN14 Mutation in a Syrian Deaf Family, Phenotypic Variations, and Comparative Analysis with the GJB2 Gene.
Tlili A, Mutery AA, Chouchen J
Genes (Basel), 15(5):588, 06 May 2024
Cited by: 0 articles | PMID: 38790217 | PMCID: PMC11121454
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Goodbye Hartmann trial: a prospective, international, multicenter, observational study on the current use of a surgical procedure developed a century ago.
Perrone G, Giuffrida M, Abu-Zidan F, Kruger VF, Livrini M, Petracca GL, Rossi G, Tarasconi A, Tian BWCA, Bonati E, Mentz R, Mazzini FN, Campana JP, Gasser E, Kafka-Ritsch R, Felsenreich DM, Dawoud C, Riss S, Gomes CA, [...] Catena F
World J Emerg Surg, 19(1):14, 16 Apr 2024
Cited by: 0 articles | PMID: 38627831 | PMCID: PMC11020610
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Glass-Like Phonon Dynamics and Thermal Transport in a GeTe Nano-Composite at Low Temperature.
Cravero R, Tlili A, Paterson J, Tomelleri M, Marcello P, Debord R, Pailhès S, Bourgeois O, Hippert F, Le Qui D, Raty JY, Noe P, Giordano VM
Small, 20(26):e2310209, 18 Apr 2024
Cited by: 0 articles | PMID: 38634392
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Fate and effects of microplastic particles in a periphyton-grazer system.
Merbt SN, Kroll A, Sgier L, Tlili A, Schirmer K, Behra R
Environ Pollut, 347:123798, 14 Mar 2024
Cited by: 0 articles | PMID: 38492748
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Mitochondrial genes modulate the phenotypic expression of congenital scoliosis syndrome caused by mutations in the TBXT gene.
Alila-Fersi O, Tej A, Maalej M, Kharrat M, Boughamoura L, Chouchen J, Tlili A, Fakhfakh F
Gene, 914:148388, 16 Mar 2024
Cited by: 0 articles | PMID: 38499212
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Expanding the genetic and phenotypic spectrum of TRAPPC9 and MID2-related neurodevelopmental disabilities: report of two novel mutations, 3D-modelling, and molecular docking studies.
Kharrat M, Triki C, Ben Isaa A, Bouchaala W, Alila O, Chouchen J, Ghouliya Y, Kamoun F, Tlili A, Fakhfakh F
J Hum Genet, 69(7):291-299, 11 Mar 2024
Cited by: 0 articles | PMID: 38467738
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Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity.
Maalej M, Sfaihi L, Fersi OA, Khabou B, Ammar M, Felhi R, Kharrat M, Chouchen J, Kammoun T, Tlili A, Fakhfakh F
Metab Brain Dis, 39(4):611-623, 16 Feb 2024
Cited by: 0 articles | PMID: 38363494
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Experimental data and modeling of sulfadiazine adsorption onto raw and modified clays from Tunisia.
Hamdi S, Mosbahi M, Issaoui M, Barreiro A, Cela-Dablanca R, Brahmi J, Tlili A, Jamoussi F, J Fernández-Sanjurjo M, Núñez-Delgado A, Álvarez-Rodríguez E, Gharbi-Khelifi H
Environ Res, 248:118309, 30 Jan 2024
Cited by: 1 article | PMID: 38301763
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Highly efficient, label free, ultrafast plasmonic SERS biosensor (silver nanoarrays/Si) to detect GJB2 gene expressed deafness mutations in real time validated with PCR studies.
A I AlSafadi A, Ramachandran K, Columbus S, Tlili A, Daoudi K, Gaidi M
Int J Biol Macromol, 259(pt 2):129381, 11 Jan 2024
Cited by: 0 articles | PMID: 38218275
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Discharge protocol in acute pancreatitis: an international survey and cohort analysis.
Nagy R, Ocskay K, Sipos Z, Szentesi A, Vincze Á, Czakó L, Izbéki F, Shirinskaya NV, Poluektov VL, Zolotov AN, Zhu Y, Xia L, He W, Sutton R, Szatmary P, Mukherjee R, Burridge IS, Wauchope E, Francisco E, [...] Hegyi P
Sci Rep, 13(1):22109, 13 Dec 2023
Cited by: 2 articles | PMID: 38092809 | PMCID: PMC10719286
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Optimization of Greedy Randomized Adaptive Search Procedure
Tlili A, Chikhi S
Preprints.org, 02 Jan 2024
Cited by: 0 articles | PPR: PPR781423
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Primary cystic echinococcosis of the peritoneum: a case report.
Kardoun N, Fendri S, Rejab H, Youssef M, Tlili A, Triki M, Toumi N, Trigui A, Boujelbene S
J Med Case Rep, 17(1):541, 14 Dec 2023
Cited by: 0 articles | PMID: 38093379 | PMCID: PMC10720152
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Timing of Cholecystectomy After Moderate and Severe Acute Biliary Pancreatitis.
Di Martino M, Ielpo B, Pata F, Pellino G, Di Saverio S, Catena F, De Simone B, Coccolini F, Sartelli M, Damaskos D, Mole D, Murzi V, Leppaniemi A, Pisanu A, Podda M, MANCTRA-1 Collaborative Group
JAMA Surg, 158(10):e233660, 11 Oct 2023
Cited by: 8 articles | PMID: 37610760 | PMCID: PMC10448376
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A Novel Mutation in the MAP7D3 Gene in Two Siblings with Severe Intellectual Disability and Autistic Traits: Concurrent Assessment of BDNF Functional Polymorphism, X-Inactivation and Oxidative Stress to Explain Disease Severity.
Kharrat M, Issa AB, Tlili A, Jallouli O, Alila-Fersi O, Maalej M, Chouchen J, Ghouylia Y, Kamoun F, Triki C, Fakhfakh F
J Mol Neurosci, 73(9-10):853-864, 10 Oct 2023
Cited by: 0 articles | PMID: 37817054
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A novel homozygous PIGO mutation associated with severe infantile epileptic encephalopathy, profound developmental delay and psychomotor retardation: structural and 3D modelling investigations and genotype-phenotype correlation.
Aguech A, Sfaihi L, Alila-Fersi O, Kolsi R, Tlili A, Kammoun T, Fendri A, Fakhfakh F
Metab Brain Dis, 38(8):2665-2678, 01 Sep 2023
Cited by: 0 articles | PMID: 37656370
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Synthesis of Fluorinated Amines: A Personal Account.
Yang Y, Taponard A, Vantourout JC, Tlili A
ACS Org Inorg Au, 3(6):364-370, 05 Sep 2023
Cited by: 1 article | PMID: 38075451 | PMCID: PMC10704584
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Photochemically Driven Nickel-Catalyzed Carboxylative C-N Coupling: Scope and Mechanism.
Abid S, Quirion KP, Yang Y, Tang R, Mai BK, Liu P, Tlili A
Chemistry, 29(44):e202301271, 06 Jul 2023
Cited by: 2 articles | PMID: 37184082
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1-25 of 187 results

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Search life-sciences literature (45,104,145 articles, preprints and more)

Suggested authors matching "AUTH:Tlili A" with an ORCID

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Identification of Genes Associated with Familial Focal Segmental Glomerulosclerosis Through Transcriptomics and In Silico Analysis, Including <i>RPL27</i>, <i>TUBB6</i>, and <i>PFDN5</i>.

Impact of missense mutations on the structure-function relationship of human succinyl-CoA synthetase using in silico analysis.

Photochemically Driven Palladium- Phosphinoacridine Catalysis: A Carboxylative Approach for Arylcarbamate Synthesis.

Formate Salt as a Bifunctional Reagent for Hydroxylation and Carbonylation Reactions Under Photochemically Driven Nickel Catalysis.

Congenital anomalies of the kidney and urinary tract.

Genetic analysis of 106 sporadic cases with hearing loss in the UAE population.

How do Chinese and Egyptian science textbooks differ? A cross-country comparative research.

Designing a Simple Electrochemical Genosensor for the Detection of Urinary PCA3, a Prostate Cancer Biomarker.

The Segregation of p.Arg68Ter-CLDN14 Mutation in a Syrian Deaf Family, Phenotypic Variations, and Comparative Analysis with the GJB2 Gene.

Goodbye Hartmann trial: a prospective, international, multicenter, observational study on the current use of a surgical procedure developed a century ago.

Glass-Like Phonon Dynamics and Thermal Transport in a GeTe Nano-Composite at Low Temperature.

Fate and effects of microplastic particles in a periphyton-grazer system.

Mitochondrial genes modulate the phenotypic expression of congenital scoliosis syndrome caused by mutations in the TBXT gene.

Expanding the genetic and phenotypic spectrum of TRAPPC9 and MID2-related neurodevelopmental disabilities: report of two novel mutations, 3D-modelling, and molecular docking studies.

Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity.

Experimental data and modeling of sulfadiazine adsorption onto raw and modified clays from Tunisia.

Highly efficient, label free, ultrafast plasmonic SERS biosensor (silver nanoarrays/Si) to detect GJB2 gene expressed deafness mutations in real time validated with PCR studies.

Discharge protocol in acute pancreatitis: an international survey and cohort analysis.

Optimization of Greedy Randomized Adaptive Search Procedure

Primary cystic echinococcosis of the peritoneum: a case report.

Timing of Cholecystectomy After Moderate and Severe Acute Biliary Pancreatitis.

A Novel Mutation in the MAP7D3 Gene in Two Siblings with Severe Intellectual Disability and Autistic Traits: Concurrent Assessment of BDNF Functional Polymorphism, X-Inactivation and Oxidative Stress to Explain Disease Severity.

A novel homozygous PIGO mutation associated with severe infantile epileptic encephalopathy, profound developmental delay and psychomotor retardation: structural and 3D modelling investigations and genotype-phenotype correlation.

Synthesis of Fluorinated Amines: A Personal Account.

Photochemically Driven Nickel-Catalyzed Carboxylative C-N Coupling: Scope and Mechanism.

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Suggested authors matching "AUTH:Tlili A" with an ORCID