Temporomandibular disorder and comorbid pain conditions

Por Lim, Pei Feng, Maixner, William, Khan, Asma A.
Publicado em 2011

The Effect of Calcium Hydroxide on Pro-Inflammatory Cytokines and Neuropeptides

Por Khan, Asma A., Sun, Xiaoling, Hargreaves, Kenneth M.
Publicado no J Endod (2008)

Endosomal TLR-8 Senses microRNA-1294 Resulting in the Production of NFḱB Dependent Cytokines

Por Pluta, Linda, Yousefi, Babak, Damania, Blossom, Khan, Asma A.
Publicado no Front Immunol (2019)

Expression of COX −1 and −2 in a Clinical Model of Acute Inflammation

Por Khan, Asma A., Iadarola, Michael, Yang, Hsiu-Ying T., Dionne, Raymond A.
Publicado em 2007

Gene expression profile of pulpitis

Por Galicia, Johnah C., Henson, Brett R., Parker, Joel S., Khan, Asma A.
Publicado no Genes Immun (2016)

The relationship between resting arterial blood pressure and acute postoperative pain in endodontic patients

Por King, James Wayne, Bair, Eric, Duggan, Derek, Maixner, William, Khan, Asma A.
Publicado em 2012

Genetic Variants in Cyclooxygenase- 2 Contribute to Post-treatment Pain among Endodontic Patients

Por Applebaum, Elizabeth, Nackley, Andrea G., Bair, Eric, Maixner, William, Khan, Asma A.
Publicado no J Endod (2015)

Genetic and Epigenetic Characterization of Pulpal and Periapical Inflammation

Por Fouad, Ashraf F., Khan, Asma A., Silva, Renato M., Kang, Mo K.
Publicado no Front Physiol (2020)

A standardized novel method to measure radiographic root changes following endodontic therapy in immature teeth

Por Flake, Natasha M., Gibbs, Jennifer L., Diogenes, Anibal, Hargreaves, Kenneth M., Khan, Asma A.
Publicado em 2013

MiRNA-181a regulates Toll-like receptor agonist-induced inflammatory response in human fibroblasts

Por Galicia, Johnah C., Naqvi, Afsar R., Ko, Ching-Chang, Nares, Salvador, Khan, Asma A.
Publicado em 2014

MicroRNA expression profiles differentiate chronic pain condition subtypes

Por Ciszek, Brittney P., Khan, Asma A., Dang, Hong, Slade, Gary D., Smith, Shad, Bair, Eric, Maixner, William, Zolnoun, Denniz, Nackley, Andrea G.
Publicado no Transl Res (2015)

A Common Ancestral Mutation in CRYBB3 Identified in Multiple Consanguineous Families with Congenital Cataracts

Por Jiao, Xiaodong, Kabir, Firoz, Irum, Bushra, Khan, Arif O., Wang, Qiwei, Li, David, Khan, Asma A., Husnain, Tayyab, Akram, Javed, Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado no PLoS One (2016)

Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

Por Jiaox, Xiaodong, Khan, Shahid Y., Irum, Bushra, Khan, Arif O., Wang, Qiwei, Kabir, Firoz, Khan, Asma A., Husnain, Tayyab, Akram, Javed, Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado no PLoS One (2015)

Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

Por Jiao, Xiaodong, Khan, Shahid Y., Irum, Bushra, Khan, Arif O., Wang, Qiwei, Kabir, Firoz, Khan, Asma A., Husnain, Tayyab, Akram, Javed, Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado no PLoS One (2017)

Mutational and Phenotypic Spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome

Por Faridi, Rabia, Tona, Risa, Brofferio, Alessandra, Hoa, Michael, Olszewski, Rafal, Schrauwen, Isabelle, Assir, Muhammad Z.K., Bandesha, Akhtar A., Khan, Asma A., Rehman, Atteeq U., Brewer, Carmen, Ahmed, Wasim, Leal, Suzanne M., Riazuddin, Sheikh, Boyden, Steven E., Friedman, Thomas B.
Publicado no Hum Mutat (2018)

Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly

Por Richard, Elodie M., Polla, Daniel L., Assir, Muhammad Zaman, Contreras, Minerva, Shahzad, Mohsin, Khan, Asma A., Razzaq, Attia, Akram, Javed, Tarar, Moazzam N., Blanpied, Thomas A., Ahmed, Zubair M., Abou Jamra, Rami, Wieczorek, Dagmar, van Bokhoven, Hans, Riazuddin, Sheikh, Riazuddin, Saima
Publicado no Am J Hum Genet (2019)

Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86

Por Rehman, Atteeq U., Santos-Cortez, Regie Lyn P., Morell, Robert J., Drummond, Meghan C., Ito, Taku, Lee, Kwanghyuk, Khan, Asma A., Basra, Muhammad Asim R., Wasif, Naveed, Ayub, Muhammad, Ali, Rana A., Raza, Syed I., Nickerson, Deborah A., Shendure, Jay, Bamshad, Michael, Riazuddin, Saima, Billington, Neil, Khan, Shaheen N., Friedman, Penelope L., Griffith, Andrew J., Ahmad, Wasim, Riazuddin, Sheikh, Leal, Suzanne M., Friedman, Thomas B.
Publicado em 2014

Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss

Por Richard, Elodie M., Santos-Cortez, Regie LP., Faridi, Rabia, Rehman, Atteeq U., Lee, Kwanghyuk, Shahzad, Mohsin, Acharya, Anushree, Khan, Asma A., Imtiaz, Ayesha, Chakchouk, Imen, Takla, Christina, Abbe, Izoduwa, Rafeeq, Maria, Liaqat, Khurram, Chaudhry, Taimur, Bamshad, Michael J., Schrauwen, Isabelle, Khan, Shaheen N., Morell, Robert J., Zafar, Saba, Ansar, Muhammad, Ahmed, Zubair M., Ahmad, Wasim, Riazuddin, Sheik, Friedman, Thomas B., Leal, Suzanne M., Riazuddin, Saima
Publicado no Hum Mutat (2018)