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Results 1 - 20 of 118  for All Library Resources

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1
Clinical impact of IDH1 mutations and MGMT methylation in adult glioblastoma
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Clinical impact of IDH1 mutations and MGMT methylation in adult glioblastoma

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.1-12 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-024-00516-3

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2
Understanding the role of adipokines and adipogenesis family in hepatocellular carcinoma
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Understanding the role of adipokines and adipogenesis family in hepatocellular carcinoma

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.1-14 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-023-00401-5

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3
Association between leukocyte telomere length and COVID-19 severity
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Association between leukocyte telomere length and COVID-19 severity

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.1-8 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-023-00415-z

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4
Novel pyrroline-5-carboxylate reductase 2 (PYCR2) mutation in an Iranian patient with hypomyelinating leukodystrophy: findings of molecular and in silico investigations
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Novel pyrroline-5-carboxylate reductase 2 (PYCR2) mutation in an Iranian patient with hypomyelinating leukodystrophy: findings of molecular and in silico investigations

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.1-8 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-023-00393-2

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5
Dipyridamole and adenosinergic pathway in Covid-19: a juice or holy grail
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Dipyridamole and adenosinergic pathway in Covid-19: a juice or holy grail

Egyptian Journal of Medical Human Genetics, 2022-12, Vol.23 (1), p.1-6 [Peer Reviewed Journal]

The Author(s) 2022 ;COPYRIGHT 2022 Springer ;The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00354-1

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6
The role of miRNA20a and miRNA320 in Iraqi patients with COVID-19: a case–control study
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The role of miRNA20a and miRNA320 in Iraqi patients with COVID-19: a case–control study

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.1-8 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-023-00451-9

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7
Association of p53 codon 72 polymorphism with weight and metabolic diseases in a Central Indian population
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Association of p53 codon 72 polymorphism with weight and metabolic diseases in a Central Indian population

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.1-9 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-024-00472-y

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8
Association of SLC30A8 rs13266634 gene polymorphism with type 2 diabetes mellitus (T2DM) in a population of Noakhali, Bangladesh: a case–control study
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Association of SLC30A8 rs13266634 gene polymorphism with type 2 diabetes mellitus (T2DM) in a population of Noakhali, Bangladesh: a case–control study

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.1-11 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-024-00484-8

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9
Retinoic Acid-Induced 1 gene variants associated with Smith–Magenis syndrome circadian phenotypes enriched in autism spectrum disorder: whole-genome sequencing study
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Retinoic Acid-Induced 1 gene variants associated with Smith–Magenis syndrome circadian phenotypes enriched in autism spectrum disorder: whole-genome sequencing study

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.55-7 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-024-00508-3

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10
ADGRG1-related polymicrogyria syndrome: report on a large consanguineous family with a novel variant and review
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ADGRG1-related polymicrogyria syndrome: report on a large consanguineous family with a novel variant and review

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.54-7 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-024-00499-1

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11
Germline variants in the Von Hippel-Lindau tumor suppressor gene in Cuban patients
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Article
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Germline variants in the Von Hippel-Lindau tumor suppressor gene in Cuban patients

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.1-6 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-024-00506-5

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12
Evaluating of the association between ABO blood groups and coronavirus disease 2019 (COVID-19) in Iraqi patients
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Evaluating of the association between ABO blood groups and coronavirus disease 2019 (COVID-19) in Iraqi patients

Egyptian Journal of Medical Human Genetics, 2020-09, Vol.21 (1), p.1-6 [Peer Reviewed Journal]

The Author(s) 2020 ;COPYRIGHT 2020 Springer ;The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-020-00097-x

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13
Explore the distribution of (rs35742686, rs3892097 and rs1065852) genetic polymorphisms of cytochrome P4502D6 gene in the Moroccan population
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Explore the distribution of (rs35742686, rs3892097 and rs1065852) genetic polymorphisms of cytochrome P4502D6 gene in the Moroccan population

Egyptian Journal of Medical Human Genetics, 2022-11, Vol.23 (1), p.1-9 [Peer Reviewed Journal]

The Author(s) 2022 ;COPYRIGHT 2022 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00369-8

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14
Genetic diversity of Mycobacterium tuberculosis isolates from northwest of Iran during COVID-19 era
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Article
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Genetic diversity of Mycobacterium tuberculosis isolates from northwest of Iran during COVID-19 era

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.1-6 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-023-00383-4

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15
Association between genetic polymorphisms and other attributing factors with lipid profiles among statin users: a cross-sectional retrospective study
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Association between genetic polymorphisms and other attributing factors with lipid profiles among statin users: a cross-sectional retrospective study

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.53-13 [Peer Reviewed Journal]

The Author(s) 2024 ;COPYRIGHT 2024 Springer ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-024-00523-4

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16
Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic backgrounds
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Article
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Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic backgrounds

Egyptian Journal of Medical Human Genetics, 2022-12, Vol.23 (1), p.1-8 [Peer Reviewed Journal]

The Author(s) 2022 ;COPYRIGHT 2022 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00374-x

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17
Mutual interaction of lncRNAs and epigenetics: focusing on cancer
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Article
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Mutual interaction of lncRNAs and epigenetics: focusing on cancer

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.1-14 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-023-00404-2

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18
In silico analysis of missense SNPs in GABRA1, GABRB1, and GABRB3 genes associated with some diseases in neurodevelopmental disorders
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Article
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In silico analysis of missense SNPs in GABRA1, GABRB1, and GABRB3 genes associated with some diseases in neurodevelopmental disorders

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.1-12 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-023-00446-6

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19
Understanding polycystic ovary syndrome in light of associated key genes
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Article
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Understanding polycystic ovary syndrome in light of associated key genes

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.1-15 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-023-00418-w

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20
Effects of ABCG2 C421A and ABCG2 G34A genetic polymorphisms on clinical outcome and response to imatinib mesylate, in Iranian chronic myeloid leukemia patients
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Effects of ABCG2 C421A and ABCG2 G34A genetic polymorphisms on clinical outcome and response to imatinib mesylate, in Iranian chronic myeloid leukemia patients

Egyptian Journal of Medical Human Genetics, 2023-12, Vol.24 (1), p.1-7 [Peer Reviewed Journal]

The Author(s) 2023 ;COPYRIGHT 2023 Springer ;ISSN: 1110-8630 ;EISSN: 2090-2441 ;DOI: 10.1186/s43042-022-00379-6

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Results 1 - 20 of 118  for All Library Resources

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