Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hafiza Noor Ul Ayan"'
Autor:
Hafiza Noor Ul Ayan, Yvonne Nitschke, Abdul Razzaq Mughal, Holger Thiele, Naveed Altaf Malik, Ijaz Hussain, Syed Muhammad Ijlal Haider, Frank Rutsch, Jeanette Erdmann, Muhammad Tariq, Zouhair Aherrahrou, Ilyas Ahmad
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract ENPP1 (ectonucleotide pyrophosphatase/phosphodiesterase 1) plays a critical role by converting extracellular ATP to AMP, generating extracellular PPi, a potential inhibitor of calcification. Pathogenic variants in the ENPP1 cause generalized
Externí odkaz:
https://doaj.org/article/99f8a7384195499cb0725455db5cf3c2
Autor:
Hafiza Noor Ul Ayan, Pir Sheeraz Ali, Asad Aslam Korejo, Holger Thiele, Peter Nürnberg, Muhammad Tariq, Syed Zahid Jamal, Jeanette Erdmann, Ilyas Ahmad
Publikováno v:
Clinical Genetics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::842562bd75fac4a76a4d61c9d11df821
https://doi.org/10.1111/cge.14321
https://doi.org/10.1111/cge.14321
Autor:
Hafiza Noor Ul Ayan, Muhammad Tariq
Genome-wide association studies (GWAS) are designed to find associations between genomic variants and a phenotype, usually a complex multifactorial disease. The idea for association studies in a large cohort was floated after linkage analysis, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6718e53d66970082e34f9e2195ad690
https://doi.org/10.2174/9789815079517122010008
https://doi.org/10.2174/9789815079517122010008
Autor:
Peter Nürnberg, Abdul Razzaq Mughal, Holger Thiele, Syed Zahid Jamal, Sheraz Jamal Khan, Shafaq Ramzan, Asad Aslam Korejo, Muhammad Tariq, Hafiza Noor Ul Ayan, Stephanie Tennstedt, Ilyas Ahmad, Shahid Mahmood Baig, Jeanette Erdmann, Aamir Ali, Matthias Munz
Publikováno v:
Genes
Volume 12
Issue 8
Genes, Vol 12, Iss 1282, p 1282 (2021)
Volume 12
Issue 8
Genes, Vol 12, Iss 1282, p 1282 (2021)
Cardiac conduction disease (CCD), which causes altered electrical impulse propagation in the heart, is a life-threatening condition with high morbidity and mortality. It exhibits genetic and clinical heterogeneity with diverse pathomechanisms, but in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a3c28b3476459faccf937653d2b7d19
Autor:
Shafaq, Ramzan, Stephanie, Tennstedt, Muhammad, Tariq, Sheraz, Khan, Hafiza, Noor Ul Ayan, Aamir, Ali, Matthias, Munz, Holger, Thiele, Asad Aslam, Korejo, Abdul Razzaq, Mughal, Syed Zahid, Jamal, Peter, Nürnberg, Shahid Mahmood, Baig, Jeanette, Erdmann, Ilyas, Ahmad
Publikováno v:
Genes
Cardiac conduction disease (CCD), which causes altered electrical impulse propagation in the heart, is a life-threatening condition with high morbidity and mortality. It exhibits genetic and clinical heterogeneity with diverse pathomechanisms, but in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a837f298442bb0c4e0a78fd0ef3c7777
https://pubmed.ncbi.nlm.nih.gov/34440456
https://pubmed.ncbi.nlm.nih.gov/34440456