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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
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March 17, 2023
Macrophages M2 polarization is involved in lapatinib-mediated chemopreventive effects in the lung cancer
Muhammad Tariq, Nadia Hussain, Kanwal Rehman, et al.
Human Mutation
|
August 27, 2009
Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies
Sibel Ugur Iseri, Robert J Osborne, Martin Farrall, et al.
Genetics Research
|
October 13, 2023
A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family
Ghazanfar Ali, Sadia Sadia, Syeda Ain-Ul-Batool, et al.
Plant Physiology and Biochemistry : PPB
|
November 30, 2025
Trait-based insights into hypercold resilient Haller's sedge (Carex halleriana Asso) along elevation gradient
Ansa Asghar, Farooq Ahmad, Mansoor Hameed, et al.
Frontiers in Genetics
|
January 20, 2026
Expanding the mutational spectrum of congenital microcephaly in Pakistani families
Sundas Farooq, Maria Asif, Ansar A Abbasi, et al.
The Journal of International Medical Research
|
February 4, 2025
Intravenous amino acids for kidney protection in patients undergoing cardiac surgery: A systematic review and meta-analysis of randomized controlled trials
Malik Waleed Zeb Khan, Aizaz Ali, Amna Hussain, et al.
Genes
|
October 23, 2021
A Homozygous <i>AKNA</i> Frameshift Variant Is Associated with Microcephaly in a Pakistani Family
Syeda Seema Waseem, Abubakar Moawia, Birgit Budde, et al.
Molecular Genetics and Genomics : MGG
|
December 23, 2016
CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly
Salil K Sukumaran, Maria Stumpf, Sarah Salamon, et al.
Medicine
|
February 23, 2024
Brain natriuretic peptide in acute heart failure and its association with glomerular filtration rate: A systematic review and meta-analysis
Hamdah Bashir Mughal, Ayesha Isani Majeed, Maria Aftab, et al.
Genes
|
January 21, 2023
Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual Disability
Maria Asif, Maryam Anayat, Faiza Tariq, et al.
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Search research articles
Search
Showing results (611-620 of 657) with videos related to
Sort By:
Page
of 66
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
March 17, 2023
Macrophages M2 polarization is involved in lapatinib-mediated chemopreventive effects in the lung cancer
Muhammad Tariq, Nadia Hussain, Kanwal Rehman, et al.
Human Mutation
|
August 27, 2009
Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies
Sibel Ugur Iseri, Robert J Osborne, Martin Farrall, et al.
Genetics Research
|
October 13, 2023
A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family
Ghazanfar Ali, Sadia Sadia, Syeda Ain-Ul-Batool, et al.
Plant Physiology and Biochemistry : PPB
|
November 30, 2025
Trait-based insights into hypercold resilient Haller's sedge (Carex halleriana Asso) along elevation gradient
Ansa Asghar, Farooq Ahmad, Mansoor Hameed, et al.
Frontiers in Genetics
|
January 20, 2026
Expanding the mutational spectrum of congenital microcephaly in Pakistani families
Sundas Farooq, Maria Asif, Ansar A Abbasi, et al.
The Journal of International Medical Research
|
February 4, 2025
Intravenous amino acids for kidney protection in patients undergoing cardiac surgery: A systematic review and meta-analysis of randomized controlled trials
Malik Waleed Zeb Khan, Aizaz Ali, Amna Hussain, et al.
Genes
|
October 23, 2021
A Homozygous <i>AKNA</i> Frameshift Variant Is Associated with Microcephaly in a Pakistani Family
Syeda Seema Waseem, Abubakar Moawia, Birgit Budde, et al.
Molecular Genetics and Genomics : MGG
|
December 23, 2016
CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly
Salil K Sukumaran, Maria Stumpf, Sarah Salamon, et al.
Medicine
|
February 23, 2024
Brain natriuretic peptide in acute heart failure and its association with glomerular filtration rate: A systematic review and meta-analysis
Hamdah Bashir Mughal, Ayesha Isani Majeed, Maria Aftab, et al.
Genes
|
January 21, 2023
Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual Disability
Maria Asif, Maryam Anayat, Faiza Tariq, et al.
Page
of 66