Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Naaila Tamkeen"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-19 (2024)
Abstract Background Turner syndrome (TS) is a rare disorder associated either with complete or partial loss of one X chromosome in women. The information on the genotype–phenotype relationship in TS is inadequate. Comparing the healthy and Turner s
Externí odkaz:
https://doaj.org/article/2480c17b574a4b69ad3d56d794cf9788
Autor:
Anam Farooqui, Alaa Alhazmi, Shafiul Haque, Naaila Tamkeen, Mahboubeh Mehmankhah, Safia Tazyeen, Sher Ali, Romana Ishrat
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-19 (2021)
Abstract The information on the genotype–phenotype relationship in Turner Syndrome (TS) is inadequate because very few specific candidate genes are linked to its clinical features. We used the microarray data of TS to identify the key regulatory ge
Externí odkaz:
https://doaj.org/article/94ede9a90ee449ef9b8933cb652f26d5
Autor:
Mohd Murshad Ahmed, Romana Ishrat, Safia Tazyeen, Aftab Alam, Anam Farooqui, Rafat Ali, Nikhat Imam, Naaila Tamkeen, Shahnawaz Ali, Md Zubbair Malik, Armiya Sultan
Publikováno v:
Bioinformatics and Biology Insights, Vol 15 (2021)
Cardiorenal syndromes constellate primary dysfunction of either heart or kidney whereby one organ dysfunction leads to the dysfunction of another. The role of several microRNAs (miRNAs) has been implicated in number of diseases, including hypertensio
Externí odkaz:
https://doaj.org/article/476c6bdd0dcb4eafb928de5dcd129d6e
Autor:
Naaila Tamkeen, Suliman Yousef AlOmar, Saeed Awad M. Alqahtani, Abdullah Al-jurayyan, Anam Farooqui, Safia Tazyeen, Nadeem Ahmad, Romana Ishrat
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Spina Bifida (SB) is a congenital spinal cord malformation. Efforts to discern the key regulators (KRs) of the SB protein-protein interaction (PPI) network are requisite for developing its successful interventions. The architecture of the SB network,
Externí odkaz:
https://doaj.org/article/af31609f45b54c78811099f26cc2bd1b
Autor:
Aftab Alam, Nikhat Imam, Mohd Murshad Ahmed, Safia Tazyeen, Naaila Tamkeen, Anam Farooqui, Md. Zubbair Malik, Romana Ishrat
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Tuberculosis (TB) is one of deadly transmissible disease that causes death worldwide; however, only 10% of people infected with Mycobacteriumtuberculosis develop disease, indicating that host genetic factors may play key role in determining susceptib
Externí odkaz:
https://doaj.org/article/31e65c687e984c9a962c6f165e64ef73
Autor:
Naaila Tamkeen, Anam Farooqui, Aftab Alam, null Najma, Safia Tazyeen, Mohd. Murshad Ahmad, Nadeem Ahmad, Romana Ishrat
Publikováno v:
Journal of Biomolecular Structure and Dynamics. :1-16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1dff96185d57d43ff37923c8b3d977b
https://doi.org/10.1080/07391102.2023.2199080
https://doi.org/10.1080/07391102.2023.2199080
Turner Syndrome (TS) is a rare disorder associated either with complete or partial loss of one X chromosome in women. Comparing the healthy and individuals with Turner Syndrome may help elucidate the mechanisms involved in TS pathophysiology. Gene ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2ccef74d9760e31d142579d483fdafd
https://doi.org/10.22541/au.167948136.63410950/v1
https://doi.org/10.22541/au.167948136.63410950/v1
Autor:
Shahnawaz Ali, Aftab Alam, Nikhat Imam, Rafat Ali, Naaila Tamkeen, Romana Ishrat, Anam Farooqui, Armiya Sultan, Safia Tazyeen, Mohd Murshad Ahmed, Zubbair Malik
Publikováno v:
Bioinformatics and Biology Insights
Bioinformatics and Biology Insights, Vol 15 (2021)
Bioinformatics and Biology Insights, Vol 15 (2021)
Cardiorenal syndromes constellate primary dysfunction of either heart or kidney whereby one organ dysfunction leads to the dysfunction of another. The role of several microRNAs (miRNAs) has been implicated in number of diseases, including hypertensio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0c510c457326a5009b05be236aaa0c0
http://europepmc.org/articles/PMC8256246
http://europepmc.org/articles/PMC8256246
Autor:
Naaila Tamkeen, Romana Ishrat, Mahboubeh Mehmankhah, Alaa Alhazmi, Sher Ali, Shafiul Haque, Anam Farooqui, Safia Tazyeen
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-19 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-19 (2021)
The information on the genotype–phenotype relationship in Turner Syndrome (TS) is inadequate because very few specific candidate genes are linked to its clinical features. We used the microarray data of TS to identify the key regulatory genes impli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::852936b3bf67996aa6b639ded322a2e2
https://doi.org/10.1038/s41598-021-90171-0
https://doi.org/10.1038/s41598-021-90171-0
Autor:
Naaila Tamkeen, Anam Farooqui, Romana Ishrat, Zubbair Malik, Safia Tazyeen, Nikhat Imam, Rafat Ali, Mohd Murshad Ahmed, Shahnawaz Ali, Aftab Alam
Publikováno v:
Bioinformation
Cardio-renal syndrome (CRS) is a rapidly recognized clinical entity which refers to the inextricably connection between heart and renal impairment, whereby abnormality to one organ directly promotes deterioration of the other one. Biological markers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b43945ce033a21e3d16e3c6b43ef298
https://pubmed.ncbi.nlm.nih.gov/34393423
https://pubmed.ncbi.nlm.nih.gov/34393423