Air pollution and associated self-reported effects on the exposed students at Malakand division, Pakistan

por Ullah, Sana, Ullah, Naeem, Rajper, Sohail Ahmed, Ahmad, Ilyas, Li, Zhongqiu
Publicado 2021

Capsicum chinense MYB Transcription Factor Genes: Identification, Expression Analysis, and Their Conservation and Diversification With Other Solanaceae Genomes

por Islam, Khushbu, Rawoof, Abdul, Ahmad, Ilyas, Dubey, Meenakshi, Momo, John, Ramchiary, Nirala
Publicado 2021

Phytomediated Selenium Nanoparticles Improved Physio-morphological, Antioxidant, and Oil Bioactive Compounds of Sesame under Induced Biotic Stress

por Ahmad, Ilyas, Younas, Zohaib, Mashwani, Zia-ur-Rehman, Raja, Naveed Iqbal, Akram, Abida
Publicado 2023

Integrated analysis of DNA methylation, transcriptome, and global metabolites in interspecific heterotic Capsicum F(1) hybrid

por Jaiswal, Vandana, Rawoof, Abdul, Gahlaut, Vijay, Ahmad, Ilyas, Chhapekar, Sushil S., Dubey, Meenakshi, Ramchiary, Nirala
Publicado 2022

Mechanistic Approaches to the Application of Nano-Zinc in the Poultry and Biomedical Industries: A Comprehensive Review of Future Perspectives and Challenges

por Younas, Zohaib, Mashwani, Zia Ur Rehman, Ahmad, Ilyas, Khan, Maarij, Zaman, Shah, Sawati, Laraib, Sohail
Publicado 2023

Plant in vitro cultures: A promising and emerging technology for the feasible production of antidiabetic metabolites in Caralluma tuberculata

por Ali, Amir, Mashwani, Zia-ur-Rehman, Ahmad, Ilyas, Raja, Naveed Iqbal, Mohammad, Sher, Khan, Safir Ullah
Publicado 2022

Comprehensive Approaches of Nanoparticles for Growth Performance and Health Benefits in Poultry: An Update on the Current Scenario

por Ahmad, Ilyas, Mashwani, Zia-Ur-Rehman, Raja, Naveed Iqbal, Kazmi, Abeer, Wahab, Abdul, Ali, Amir, Younas, Zohaib, Yaqoob, Saman, Rahimi, Mehdi
Publicado 2022

A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family

por Ahmad, Ilyas, Khan, Ayaz, Noor Ul Ayan, Hafiza, Budde, Birgit, Altmüller, Janine, Korejo, Asad Aslam, Nürnberg, Gudrun, Thiele, Holger, Tariq, Muhmmad, Nürnberg, Peter, Erdmann, Jeanette
Publicado 2022

Report of Hermansky–Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes

por Zaman, Qaiser, Sadeeda, Anas, Muhammad, Rehman, Gauhar, Khan, Qadeem, Iftikhar, Aiman, Ahmad, Mashal, Owais, Muhammad, Ahmad, Ilyas, Muthaffar, Osama Yousef, Abdulkareem, Angham Abdulrhman, Bibi, Fehmida, Jelani, Musharraf, Naseer, Muhammad Imran
Publicado 2023

The interleukin-11 receptor variant p.W307R results in craniosynostosis in humans

por Ahmad, Ilyas, Lokau, Juliane, Kespohl, Birte, Malik, Naveed Altaf, Baig, Shahid Mahmood, Hartig, Roland, Behme, Daniel, Schwab, Roland, Altmüller, Janine, Jameel, Muhammad, Mucha, Sören, Thiele, Holger, Tariq, Muhammad, Nürnberg, Peter, Erdmann, Jeanette, Garbers, Christoph
Publicado 2023

A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family

por Ramzan, Shafaq, Tennstedt, Stephanie, Tariq, Muhammad, Khan, Sheraz, Noor Ul Ayan, Hafiza, Ali, Aamir, Munz, Matthias, Thiele, Holger, Korejo, Asad Aslam, Mughal, Abdul Razzaq, Jamal, Syed Zahid, Nürnberg, Peter, Baig, Shahid Mahmood, Erdmann, Jeanette, Ahmad, Ilyas
Publicado 2021

Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot–Marie–Tooth and Spastic Ataxia of Charlevoix–Saguenay Type Diseases

por Zaman, Qaiser, Khan, Muhammad Abbas, Sahar, Kalsoom, Rehman, Gauhar, Khan, Hamza, Rehman, Mehwish, Najumuddin, Ahmad, Ilyas, Tariq, Muhmmad, Muthaffar, Osama Yousef, Abdulkareem, Angham Abdulrhman, Bibi, Fehmida, Naseer, Muhammad Imran, Faisal, Muhammad Shah, Wasif, Naveed, Jelani, Musharraf
Publicado 2023

CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly

por Sukumaran, Salil K., Stumpf, Maria, Salamon, Sarah, Ahmad, Ilyas, Bhattacharya, Kurchi, Fischer, Sarah, Müller, Rolf, Altmüller, Janine, Budde, Birgit, Thiele, Holger, Tariq, Muhammad, Malik, Naveed Altaf, Nürnberg, Peter, Baig, Shahid Mahmood, Hussain, Muhammad Sajid, Noegel, Angelika A.
Publicado 2016

An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan

por Rasool, Sajida, Baig, Jamshaid Mahmood, Moawia, Abubakar, Ahmad, Ilyas, Iqbal, Maria, Waseem, Syeda Seema, Asif, Maria, Abdullah, Uzma, Makhdoom, Ehtisham Ul Haq, Kaygusuz, Emrah, Zakaria, Muhammad, Ramzan, Shafaq, Haque, Saif ul, Mir, Asif, Anjum, Iram, Fiaz, Mehak, Ali, Zafar, Tariq, Muhammad, Saba, Neelam, Hussain, Wajid, Budde, Birgit, Irshad, Saba, Noegel, Angelika Anna, Höning, Stefan, Baig, Shahid Mahmood, Nürnberg, Peter, Hussain, Muhammad Sajid
Publicado 2020

Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy

por Martin, Carol-Anne, Ahmad, Ilyas, Klingseisen, Anna, Hussain, Muhammad Sajid, Bicknell, Louise S, Leitch, Andrea, Nürnberg, Gudrun, Toliat, Mohammad Reza, Murray, Jennie E, Hunt, David, Khan, Fawad, Ali, Zafar, Tinschert, Sigrid, Ding, James, Keith, Charlotte, Harley, Margaret E, Heyn, Patricia, Müller, Rolf, Hoffmann, Ingrid, Cormier-Daire, Valérie, Dollfus, Hélène, Dupuis, Lucie, Bashamboo, Anu, McElreavey, Kenneth, Kariminejad, Ariana, Mendoza-Londono, Roberto, Moore, Anthony T, Saggar, Anand, Schlechter, Catie, Weleber, Richard, Thiele, Holger, Altmüller, Janine, Höhne, Wolfgang, Hurles, Matthew E, Noegel, Angelika Anna, Baig, Shahid Mahmood, Nürnberg, Peter, Jackson, Andrew P
Publicado 2014