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The Archaeome's Role in Colorectal Cancer: Unveiling the DPANN Group and Investigating Archaeal Functional Signatures.
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- Microorganisms, 2023, v. 11, n. 11, p. 2742, doi. 10.3390/microorganisms11112742
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Virulence Factors in Colorectal Cancer Metagenomes and Association of Microbial Siderophores with Advanced Stages.
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- Microorganisms, 2022, v. 10, n. 12, p. 2365, doi. 10.3390/microorganisms10122365
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Can leukocytospermia predict prostate cancer via its effects on mitochondrial DNA?
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- Andrologia, 2021, v. 53, n. 8, p. 1, doi. 10.1111/and.14129
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Detection of a novel mutation in a Tunisian child with polycystic kidney disease.
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- IUBMB Life, 2020, v. 72, n. 8, p. 1799, doi. 10.1002/iub.2309
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- Article
A novel de novo splicing mutation c.1444‐2A>T in the TSC2 gene causes exon skipping and premature termination in a patient with tuberous sclerosis syndrome.
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- IUBMB Life, 2019, v. 71, n. 12, p. 1937, doi. 10.1002/iub.2134
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Analysis of Genetic Alterations in Tunisian Patients with Lung Adenocarcinoma.
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- Cells (2073-4409), 2019, v. 8, n. 6, p. 514, doi. 10.3390/cells8060514
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A novel C-terminal truncated mutation in hCDKL5 protein causing a severe West syndrome: Comparison with previous truncated mutations and genotype/phenotype correlation.
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- International Journal of Developmental Neuroscience, 2019, v. 72, p. 22, doi. 10.1016/j.ijdevneu.2018.09.006
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Clinical, Molecular, and Computational Analysis Showed a Novel Homozygous Mutation Among the Substrate-Binding Site of ARSA Protein in Consanguineous Family with Late-Infantile MLD.
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- Journal of Molecular Neuroscience, 2018, v. 66, n. 1, p. 17, doi. 10.1007/s12031-018-1141-z
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Thyroid Hypoplasia in Congenital Hypothyroidism Associated with Thyroid Peroxidase Mutations.
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- Thyroid, 2018, v. 28, n. 7, p. 941, doi. 10.1089/thy.2017.0502
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Do GSTM1 and GSTT1 polymorphisms influence the risk of developing mitochondrial diseases in a Tunisian population?
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- Environmental Science & Pollution Research, 2018, v. 25, n. 6, p. 5779, doi. 10.1007/s11356-017-0775-7
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Clinical, Molecular, and Computational Analysis in Patients With a Novel Double Mutation and a New Synonymous Variant in MeCP2: Report of the First Missense Mutation Within the AT-hook1 Cluster in Rett Syndrome.
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- Journal of Child Neurology, 2017, v. 32, n. 8, p. 694, doi. 10.1177/0883073817701622
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- Article
Routine assessment of occupational exposure and its relation to semen quality in infertile men: a cross-sectional study.
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- Turkish Journal of Medical Sciences, 2017, v. 47, n. 3, p. 902, doi. 10.3906/sag-1605-47
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Phenotypic variability in two infants sharing the same MECP2 mutation: evidence of chromosomal rearrangements and high sister-chromatid exchange levels in Rett syndrome.
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- Acta Neurologica Belgica, 2017, v. 117, n. 1, p. 251, doi. 10.1007/s13760-016-0667-5
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Variabilité inter et intra-opérateur de l’analyse des paramètres spermatiques: résultat d’un programme de contrôle de qualité.
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- Pan African Medical Journal, 2016, v. 25, p. 1, doi. 10.11604/pamj.2016.25.115.9158
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- Article
Fertility outcome in male and female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
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- Middle East Fertility Society Journal, 2014, v. 19, n. 2, p. 89, doi. 10.1016/j.mefs.2013.05.006
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- Article
Identification of a novel m.9588G > A missense mutation in the mitochondrial COIII gene in asthenozoospermic Tunisian infertile men.
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- Journal of Assisted Reproduction & Genetics, 2014, v. 31, n. 5, p. 595, doi. 10.1007/s10815-014-0187-2
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Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men.
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- Molecular Biology Reports, 2013, v. 40, n. 8, p. 4705, doi. 10.1007/s11033-013-2566-7
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A novel m.6307A>G mutation in the mitochondrial COXI gene in asthenozoospermic infertile men.
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- Molecular Reproduction & Development, 2013, v. 80, n. 7, p. 581, doi. 10.1002/mrd.22197
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Chromosomal defects in infertile men with poor semen quality.
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- Journal of Assisted Reproduction & Genetics, 2012, v. 29, n. 5, p. 451, doi. 10.1007/s10815-012-9737-7
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Dimethoate-induced oxidative stress in human erythrocytes and the protective effect of Vitamins C and E in vitro.
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- Environmental Toxicology, 2011, v. 26, n. 3, p. 287, doi. 10.1002/tox.20555
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Sperm DNA fragmentation and oxidation are independent of malondialdheyde.
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- Reproductive Biology & Endocrinology, 2011, v. 9, n. 1, p. 47, doi. 10.1186/1477-7827-9-47
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Genetic association between AZF region polymorphism and Klinefelter syndrome.
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- Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2009, v. 19, n. 4, p. 547, doi. 10.1016/j.rbmo.2009.05.006
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Lipid peroxidation and antioxidant enzyme activities in infertile men: correlation with semen parameter.
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- Journal of Clinical Laboratory Analysis, 2009, v. 23, n. 2, p. 99, doi. 10.1002/jcla.20297
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Combining Autosomal and Y-Chromosomal Short Tandem Repeat Data in Paternity Testing with Male Child: Methods and Application.
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- Journal of Forensic Sciences, 2007, v. 52, n. 5, p. 1068, doi. 10.1111/j.1556-4029.2007.00513.x
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