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Blood Cells, Molecules & Diseases
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May 30, 2025
Thalidomide confers therapeutic benefit in beta thalassemia patients by enhancing hemoglobin and hematopoietic gene expression: A non-randomized clinical trial
Inayat Ur Rahman, Muhammad Tariq Masood Khan, Zahid Ali, et al.
Veterinary World
|
November 7, 2024
Prevalence of trypanosomiasis caused by <i>Trypanosoma evansi</i> (Kinetoplastea, <i>Trypanosomatidae</i>) in domestic ruminants from Southern Punjab, Pakistan
Muhammad Tariq, Farhad Badshah, Muhammad Salman Khan, et al.
Plant Physiology and Biochemistry : PPB
|
May 15, 2020
Deciphering metal toxicity responses of flax (Linum usitatissimum L.) with exopolysaccharide and ACC-deaminase producing bacteria in industrially contaminated soils
Nida Zainab, Amna, Bashir Ud Din, et al.
Patient Education and Counseling
|
June 4, 2025
A cross-sectional study to assess patients' perception of physicians' communication skills: 15 minutes is what it takes
Namra Qadeer Shaikh, Noreen Afzal, Komal Abdul Rahim, et al.
Human Genetics
|
October 14, 2021
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss
Farid Ullah, Waqar Rauf, Kamal Khan, et al.
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.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
July 9, 2019
Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families
Shumaila Zulfiqar, Muhammad Tariq, Zafar Ali, et al.
Genes
|
August 27, 2021
A Novel Missense Mutation in <i>TNNI3K</i> Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family
Shafaq Ramzan, Stephanie Tennstedt, Muhammad Tariq, et al.
International Journal of Biological Macromolecules
|
November 7, 2021
Kinetically modelled approach of xanthan production using different carbon sources: A study on molecular weight and rheological properties of xanthan
Ali Mohsin, Kanagat Akbota Akyliyaevna, Waqas Qamar Zaman, 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.
Page
of 95
Search research articles
Search
Showing results (901-910 of 945) with videos related to
Sort By:
Page
of 95
Blood Cells, Molecules & Diseases
|
May 30, 2025
Thalidomide confers therapeutic benefit in beta thalassemia patients by enhancing hemoglobin and hematopoietic gene expression: A non-randomized clinical trial
Inayat Ur Rahman, Muhammad Tariq Masood Khan, Zahid Ali, et al.
Veterinary World
|
November 7, 2024
Prevalence of trypanosomiasis caused by <i>Trypanosoma evansi</i> (Kinetoplastea, <i>Trypanosomatidae</i>) in domestic ruminants from Southern Punjab, Pakistan
Muhammad Tariq, Farhad Badshah, Muhammad Salman Khan, et al.
Plant Physiology and Biochemistry : PPB
|
May 15, 2020
Deciphering metal toxicity responses of flax (Linum usitatissimum L.) with exopolysaccharide and ACC-deaminase producing bacteria in industrially contaminated soils
Nida Zainab, Amna, Bashir Ud Din, et al.
Patient Education and Counseling
|
June 4, 2025
A cross-sectional study to assess patients' perception of physicians' communication skills: 15 minutes is what it takes
Namra Qadeer Shaikh, Noreen Afzal, Komal Abdul Rahim, et al.
Human Genetics
|
October 14, 2021
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss
Farid Ullah, Waqar Rauf, Kamal Khan, et al.
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.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
July 9, 2019
Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families
Shumaila Zulfiqar, Muhammad Tariq, Zafar Ali, et al.
Genes
|
August 27, 2021
A Novel Missense Mutation in <i>TNNI3K</i> Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family
Shafaq Ramzan, Stephanie Tennstedt, Muhammad Tariq, et al.
International Journal of Biological Macromolecules
|
November 7, 2021
Kinetically modelled approach of xanthan production using different carbon sources: A study on molecular weight and rheological properties of xanthan
Ali Mohsin, Kanagat Akbota Akyliyaevna, Waqas Qamar Zaman, 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.
Page
of 95