MicroRNA-125b-5p regulates IL-1β induced inflammatory genes via targeting TRAF6-mediated MAPKs and NF-κB signaling in human osteoarthritic chondrocytes

por Rasheed, Zafar, Rasheed, Naila, Abdulmonem, Waleed Al, Khan, Muhammad Ismail
Publicado 2019

Author Correction: MicroRNA-125b-5p regulates IL-1β induced inflammatory genes via targeting TRAF6-mediated MAPKs and NF-κB signaling in human osteoarthritic chondrocytes

por Rasheed, Zafar, Rasheed, Naila, Abdulmonem, Waleed Al, Khan, Muhammad Ismail
Publicado 2019

Hydroxyl Radical Modification of Immunoglobulin G Generated Cross-Reactive Antibodies: Its Potential Role in Systemic Lupus Erythematosus

por Al-Shobaili, Hani A., Al Robaee, Ahmad A., Alzolibani, Abdullateef, Khan, Muhammad Ismail, Rasheed, Zafar
Publicado 2011

Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

por Khan, Amjad, Wang, Rongrong, Han, Shirui, Umair, Muhammad, Abbas, Safdar, Khan, Muhammad Ismail, Alshabeeb, Mohammad A., Alfadhel, Majid, Zhang, Xue
Publicado 2019

Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

por Khan, Amjad, Wang, Rongrong, Han, Shirui, Umair, Muhammad, Abbas, Safdar, Khan, Muhammad Ismail, Alshabeeb, Mohammad A., Alfadheland, Majid, Zhang, Xue
Publicado 2019

Novel homozygous variant in the TPO gene associated with congenital hypothyroidism and mild-intellectual disability

por Khan, Amjad, Umair, Muhammad, Sharaf, Rania Abdulfattah, Khan, Muhammad Ismail, Ullah, Amir, Abbas, Safdar, Shaheen, Nargis, Bilal, Muhammad, Ahamd, Farooq
Publicado 2020

Interleukin-6 polymorphisms in HCC patients chronically infected with HCV

por Adnan, Faisal, Khan, Najeeb Ullah, Iqbal, Aqib, Ali, Ijaz, Petruzziello, Arnolfo, Sabatino, Rocco, Guzzo, Annunziata, Loquercio, Giovanna, Botti, Gerardo, Khan, Sanaullah, Naeem, Muhammad, Khan, Muhammad Ismail
Publicado 2020

Biallelic inheritance in a single Pakistani family with intellectual disability implicates new candidate gene RDH14

por Pastore, Stephen F., Muhammad, Tahir, Harripaul, Ricardo, Lau, Rebecca, Khan, Muhammad Tariq Masood, Khan, Muhammad Ismail, Islam, Omar, Kang, Changsoo, Ayub, Muhammad, Jelani, Musharraf, Vincent, John B.
Publicado 2021

Highly Recurrent Copy Number Variations in GABRB2 Associated With Schizophrenia and Premenstrual Dysphoric Disorder

por Ullah, Ata, Long, Xi, Mat, Wai-Kin, Hu, Taobo, Khan, Muhammad Ismail, Hui, Li, Zhang, Xiangyang, Sun, Peng, Gao, Mingzhou, Wang, Jieqiong, Wang, Haijun, Li, Xia, Sun, Wenjun, Qiao, Mingqi, Xue, Hong
Publicado 2020

A mutation in the major autophagy gene, WIPI2, associated with global developmental abnormalities

por Jelani, Musharraf, Dooley, Hannah C., Gubas, Andrea, Mohamoud, Hussein Sheikh Ali, Khan, Muhammad Tariq Masood, Ali, Zahir, Kang, Changsoo, Rahim, Fazal, Jan, Amin, Vadgama, Nirmal, Khan, Muhammad Ismail, Al-Aama, Jumana Yousuf, Khan, Asifullah, Tooze, Sharon A, Nasir, Jamal
Publicado 2019