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Evidence for Association of the E23K Variant of KCNJ11 Gene with Type 2 Diabetes in Tunisian Population: Population-Based Study and Meta-Analysis.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Evidence for Association of the E23K Variant of KCNJ11 Gene with Type 2 Diabetes in Tunisian Population: Population-Based Study and Meta-Analysis.
- Published in:
- BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/265274
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- Publication type:
- Article
Branched-Chain Amino Acid Database Integrated in MEDIPAD Software as a Tool for Nutritional Investigation of Mediterranean Populations.
- Published in:
- Nutrients, 2018, v. 10, n. 10, p. 1392, doi. 10.3390/nu10101392
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- Publication type:
- Article
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family.
- Published in:
- Human Heredity, 2020, v. 85, n. 1, p. 35, doi. 10.1159/000512712
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- Publication type:
- Article
A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational Analysis.
- Published in:
- Human Heredity, 2019, v. 84, n. 6, p. 272, doi. 10.1159/000510062
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- Publication type:
- Article
Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.
- Published in:
- Human Heredity, 2019, v. 84, n. 3, p. 109, doi. 10.1159/000503450
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- Publication type:
- Article
Chromosomal Abnormalities in Patients with Intellectual Disability: A 21-Year Retrospective Study.
- Published in:
- Human Heredity, 2018, v. 83, n. 5, p. 274, doi. 10.1159/000499710
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- Publication type:
- Article
Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene Polymorphism with Coronary Artery Disease in Moroccan Subjects: A Case-Control Study and an Updated Meta-Analysis.
- Published in:
- Cardiology Research & Practice, 2020, p. 1, doi. 10.1155/2020/5981971
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- Publication type:
- Article
Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis.
- Published in:
- Diabetology & Metabolic Syndrome, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13098-022-00794-0
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- Publication type:
- Article
The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 3, p. 322, doi. 10.1038/ejhg.2013.151
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- Publication type:
- Article
AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men.
- Published in:
- Asian Journal of Andrology, 2007, v. 9, n. 5, p. 674, doi. 10.1111/j.1745-7262.2007.00290.x
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- Publication type:
- Article
An Unusual Case of Gullo’s Syndrome Concomitant with Serious Endometriosis Disease in a Postmenopausal Woman.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the<bold><italic> R-spondin1 </italic></bold>Gene Associated with Familial 46,XX DSD.
- Published in:
- Sexual Development, 2017, v. 11, n. 5/6, p. 269, doi. 10.1159/000485393
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- Publication type:
- Article
Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile.
- Published in:
- BMC Research Notes, 2017, v. 10, p. 1, doi. 10.1186/s13104-017-3042-6
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- Publication type:
- Article
Clinical and genetic investigations of three Moroccan families with retinitis pigmentosa phenotypes.
- Published in:
- Molecular Vision, 2021, v. 27, p. 17
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- Publication type:
- Article
Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 3, p. 499, doi. 10.1007/s10815-018-1373-4
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- Publication type:
- Article
In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure.
- Published in:
- Journal of Diabetes Research, 2019, p. 1, doi. 10.1155/2019/4951627
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- Publication type:
- Article
H Syndrome: Two new morrocan cases.
- Published in:
- Our Dermatology Online / Nasza Dermatologia Online, 2022, v. 13, p. 49, doi. 10.7241/ourd.2022S2.6
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- Publication type:
- Article
H Syndrome: Two new morrocan cases.
- Published in:
- Our Dermatology Online / Nasza Dermatologia Online, 2022, v. 13, p. 49, doi. 10.7241/ourd.2022S2.6
- By:
- Publication type:
- Article
Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa.
- Published in:
- Bioscience Reports, 2020, v. 40, n. 8, p. 1, doi. 10.1042/BSR20200706
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- Publication type:
- Article
Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families.
- Published in:
- Journal of Clinical Immunology, 2020, v. 40, n. 1, p. 96, doi. 10.1007/s10875-019-00706-4
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- Publication type:
- Article
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 3, p. 187, doi. 10.1007/s10875-016-0251-z
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- Publication type:
- Article
Molecular Modelling and Dynamics Study of nsSNP in STXBP1 Gene in Early Infantile Epileptic Encephalopathy Disease.
- Published in:
- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/4872101
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- Publication type:
- Article
Prediction and Structural Comparison of Deleterious Coding Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in Human LEP Gene Associated with Obesity.
- Published in:
- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/1832084
- By:
- Publication type:
- Article
Association of Spermatogenic Failure with the b2/b3 Partial AZFc Deletion.
- Published in:
- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0034902
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- Publication type:
- Article
Association of the MTHFR A1298C Variant with Unexplained Severe Male Infertility.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0034111
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- Publication type:
- Article
Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09740-x
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- Publication type:
- Article
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.
- Published in:
- Biochemical Genetics, 2024, v. 62, n. 3, p. 1914, doi. 10.1007/s10528-023-10515-5
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- Publication type:
- Article
Genetic Association of LEP Gene Polymorphisms with Obesity in Moroccan Individuals: Case–Control Study and Updated Meta-analysis.
- Published in:
- Biochemical Genetics, 2023, v. 61, n. 5, p. 1758, doi. 10.1007/s10528-023-10342-8
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- Publication type:
- Article
Association Analysis of IGF2BP2, KCNJ11, and CDKAL1 Polymorphisms with Type 2 Diabetes Mellitus in a Moroccan Population: A Case-Control Study and Meta-analysis.
- Published in:
- Biochemical Genetics, 2014, v. 52, n. 9/10, p. 430, doi. 10.1007/s10528-014-9658-5
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- Publication type:
- Article
Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.
- Published in:
- Lipids in Health & Disease, 2014, v. 13, n. 1, p. 60, doi. 10.1186/1476-511X-13-60
- By:
- Publication type:
- Article
A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report.
- Published in:
- 2015
- By:
- Publication type:
- journal article
The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
- Published in:
- PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0176516
- By:
- Publication type:
- Article
Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Identification of a novel BLM missense mutation (2706T>C) in a Moroccan patient with Bloom's syndrome.
- Published in:
- Human Mutation, 2000, v. 15, n. 6, p. 584, doi. 10.1002/1098-1004(200006)15:6<584::AID-HUMU28>3.0.CO;2-I
- By:
- Publication type:
- Article
Computational Analysis of nsSNPs of Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study.
- Published in:
- BioMed Research International, 2020, p. 1, doi. 10.1155/2020/7614634
- By:
- Publication type:
- Article
Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients.
- Published in:
- BMC Cancer, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12885-015-1040-4
- By:
- Publication type:
- Article
Clinicopathological Features and Molecular Analysis of Primary Glioblastomas in Moroccan Patients.
- Published in:
- Journal of Molecular Neuroscience, 2013, v. 49, n. 3, p. 567, doi. 10.1007/s12031-012-9868-4
- By:
- Publication type:
- Article
Novel pathogenic WHRN variant causing hearing loss in a moroccan family.
- Published in:
- Molecular Biology Reports, 2023, v. 50, n. 12, p. 10663, doi. 10.1007/s11033-023-08901-8
- By:
- Publication type:
- Article
First characterization of congenital myasthenic syndrome type 5 in North Africa.
- Published in:
- Molecular Biology Reports, 2021, v. 48, n. 10, p. 6999, doi. 10.1007/s11033-021-06530-7
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- Publication type:
- Article
Novel compound heterozygous mutations in the GPR98 ( USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.
- Published in:
- Molecular Biology Reports, 2017, v. 44, n. 5, p. 429, doi. 10.1007/s11033-017-4129-9
- By:
- Publication type:
- Article
TNF A −308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis.
- Published in:
- Molecular Biology Reports, 2014, v. 41, n. 9, p. 5805, doi. 10.1007/s11033-014-3454-5
- By:
- Publication type:
- Article
The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.
- Published in:
- Molecular Biology Reports, 2012, v. 39, n. 12, p. 11011, doi. 10.1007/s11033-012-2003-3
- By:
- Publication type:
- Article
Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.
- Published in:
- Human Mutation, 2015, v. 36, n. 11, p. E2441, doi. 10.1002/humu.22835
- By:
- Publication type:
- Article
GNE Myopathy and Duchenne Muscular Dystrophy in Two Moroccans Families.
- Published in:
- Muscles, Ligaments & Tendons Journal (MLTJ), 2023, v. 13, n. 4, p. 653, doi. 10.32098/mltj.04.2023.18
- By:
- Publication type:
- Article
Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21‐year single‐center experience.
- Published in:
- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 8, p. 1516, doi. 10.1002/ajmg.a.61257
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- Publication type:
- Article
Contribution of CDKAL1 rs7756992 and IGF2BP2 rs4402960 polymorphisms in type 2 diabetes, diabetic complications, obesity risk and hypertension in the Tunisian population 在突尼斯人群中, CDKAL1 rs7756992与 IGF2BP2 rs4402960的多态性对2型糖尿病、糖尿病并发症、肥胖风险以及高血压的影响
- Published in:
- Journal of Diabetes, 2015, v. 7, n. 1, p. 102, doi. 10.1111/1753-0407.12147
- By:
- Publication type:
- Article
c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.
- Published in:
- Archives of Dermatological Research, 2013, v. 305, n. 1, p. 53, doi. 10.1007/s00403-012-1299-0
- By:
- Publication type:
- Article