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Heliyon
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September 17, 2024
Discovery of a novel mutation F184S (c.551T>C) in GATA4 gene causing congenital heart disease in a consanguineous Saudi family
Mahmood Rasool, Peter Natesan Pushparaj, Absarul Haque, et al.
CNS & Neurological Disorders Drug Targets
|
September 25, 2013
A nanotechnological approach to the management of Alzheimer disease and type 2 diabetes
Qamre Alam, Mohammad ZubairAlam, Sajjad Karim, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 5, 2018
A novel homozygous nonsense mutation in CCDC88A gene cause PEHO-like syndrome in consanguineous Saudi family
Angham Abdulrahman Abdulkareem, Khalid Omar Abulnaja, Mohammad M Jan, et al.
Cancer Cell International
|
January 23, 2025
The mutational spectrum of NRAS gene discovers a novel frameshift mutation (E49R) in Saudi colorectal cancer patients
Mahmood Rasool, Absarul Haque, Mohammed Alharthi, et al.
Bioinformation
|
June 22, 2019
Genomic amplification of chromosome 7 in the Doxorubicin resistant K562 cell line
Sara M Ibrahim, Sajjad Karim, Heba Abusamra, et al.
Anticancer Research
|
March 6, 2014
Expression of matrix metalloproteinases (MMPs) in primary human breast cancer: MMP-9 as a potential biomarker for cancer invasion and metastasis
Adnan Merdad, Sajjad Karim, Hans-Juergen Schulten, et al.
Plos One
|
March 20, 2015
Molecular interaction of a kinase inhibitor midostaurin with anticancer drug targets, S100A8 and EGFR: transcriptional profiling and molecular docking study for kidney cancer therapeutics
Zeenat Mirza, Hans-Juergen Schulten, Hasan Ma Farsi, et al.
Life (Basel, Switzerland)
|
January 21, 2022
Two Novel Homozygous <i>HPS6</i> Mutations (Double Mutant) Identified by Whole-Exome Sequencing in a Saudi Consanguineous Family Suspected for Oculocutaneous Albinism
Sajjad Karim, Samah Saharti, Nofe Alganmi, et al.
BMC Genomics
|
October 22, 2016
e-GRASP: an integrated evolutionary and GRASP resource for exploring disease associations
Sajjad Karim, Hend Fakhri NourEldin, Heba Abusamra, et al.
Asian Pacific Journal of Cancer Prevention : APJCP
|
December 19, 2012
CA 15-3 (Mucin-1) and physiological characteristics of breast cancer from Lahore, Pakistan
Mumtaz Begum, Sajjad Karim, Arif Malik, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 81) with videos related to
Sort By:
Page
of 9
Heliyon
|
September 17, 2024
Discovery of a novel mutation F184S (c.551T>C) in GATA4 gene causing congenital heart disease in a consanguineous Saudi family
Mahmood Rasool, Peter Natesan Pushparaj, Absarul Haque, et al.
CNS & Neurological Disorders Drug Targets
|
September 25, 2013
A nanotechnological approach to the management of Alzheimer disease and type 2 diabetes
Qamre Alam, Mohammad ZubairAlam, Sajjad Karim, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 5, 2018
A novel homozygous nonsense mutation in CCDC88A gene cause PEHO-like syndrome in consanguineous Saudi family
Angham Abdulrahman Abdulkareem, Khalid Omar Abulnaja, Mohammad M Jan, et al.
Cancer Cell International
|
January 23, 2025
The mutational spectrum of NRAS gene discovers a novel frameshift mutation (E49R) in Saudi colorectal cancer patients
Mahmood Rasool, Absarul Haque, Mohammed Alharthi, et al.
Bioinformation
|
June 22, 2019
Genomic amplification of chromosome 7 in the Doxorubicin resistant K562 cell line
Sara M Ibrahim, Sajjad Karim, Heba Abusamra, et al.
Anticancer Research
|
March 6, 2014
Expression of matrix metalloproteinases (MMPs) in primary human breast cancer: MMP-9 as a potential biomarker for cancer invasion and metastasis
Adnan Merdad, Sajjad Karim, Hans-Juergen Schulten, et al.
Plos One
|
March 20, 2015
Molecular interaction of a kinase inhibitor midostaurin with anticancer drug targets, S100A8 and EGFR: transcriptional profiling and molecular docking study for kidney cancer therapeutics
Zeenat Mirza, Hans-Juergen Schulten, Hasan Ma Farsi, et al.
Life (Basel, Switzerland)
|
January 21, 2022
Two Novel Homozygous <i>HPS6</i> Mutations (Double Mutant) Identified by Whole-Exome Sequencing in a Saudi Consanguineous Family Suspected for Oculocutaneous Albinism
Sajjad Karim, Samah Saharti, Nofe Alganmi, et al.
BMC Genomics
|
October 22, 2016
e-GRASP: an integrated evolutionary and GRASP resource for exploring disease associations
Sajjad Karim, Hend Fakhri NourEldin, Heba Abusamra, et al.
Asian Pacific Journal of Cancer Prevention : APJCP
|
December 19, 2012
CA 15-3 (Mucin-1) and physiological characteristics of breast cancer from Lahore, Pakistan
Mumtaz Begum, Sajjad Karim, Arif Malik, et al.
Page
of 9