Evaluation of sucrose esters as alternative surfactants in microencapsulation of proteins by the solvent evaporation method

Por Youan, Bi-Botti C., Hussain, Alamdar, Nguyen, Nga T.
Publicado em 2003

Remediation of Hemorrhagic Shock-Induced Intestinal Barrier Dysfunction by Treatment with Diphenyldihaloketones EF24 and CLEFMA

Por Yadav, Vivek R., Hussain, Alamdar, Sahoo, Kaustuv, Awasthi, Vibhudutta
Publicado em 2014

The salutary effects of diphenyldifluoroketone EF24 in liver of a rat hemorrhagic shock model

Por Yadav, Vivek R, Hussain, Alamdar, Xie, Jun, Kosanke, Stanley, Awasthi, Vibhudutta
Publicado no Scand J Trauma Resusc Emerg Med (2015)

Positively Charged Polyethylenimines Enhance Nasal Absorption of the Negatively Charged Drug, Low Molecular Weight Heparin

Por Yang, Tianzhi, Hussain, Alamdar, Bai, Shuhua, Khalil, Ikramy A., Harashima, Hideyoshi, Ahsan, Fakhrul
Publicado em 2006

The brain metabolic activity after resuscitation with liposome-encapsulated hemoglobin in a rat model of hypovolemic shock

Por Rao, Geeta, Hedrick, Andria F, Yadav, Vivek R, Xie, Jun, Hussain, Alamdar, Awasthi, Vibhudutta
Publicado no J Cereb Blood Flow Metab (2015)

Dual Phosphorylation of Btk by Akt/Protein Kinase B Provides Docking for 14-3-3ζ, Regulates Shuttling, and Attenuates both Tonic and Induced Signaling in B Cells

Por Mohammad, Dara K., Nore, Beston F., Hussain, Alamdar, Gustafsson, Manuela O., Mohamed, Abdalla J., Smith, C. I. Edvard
Publicado em 2013

Comprehensive Registration of DNA Sequence Variants Associated with Inherited Retinal Diseases in Leiden Open Variation Databases

Por Cremers, Frans P. M., den Dunnen, Johan T., Ajmal, Muhammad, Hussain, Alamdar, Preising, Markus N., Daiger, Stephen P., Qamar, Raheel
Publicado em 2014

Signaling of the ITK (Interleukin 2-inducible T Cell Kinase)-SYK (Spleen Tyrosine Kinase) Fusion Kinase Is Dependent on Adapter SLP-76 and on the Adapter Function of the Kinases SY...

Por Hussain, Alamdar, Mohammad, Dara K., Gustafsson, Manuela O., Uslu, Merve, Hamasy, Abdulrahman, Nore, Beston F., Mohamed, Abdalla J., Smith, C. I. Edvard
Publicado em 2013

Regulation of Nucleocytoplasmic Shuttling of Bruton's Tyrosine Kinase (Btk) through a Novel SH3-Dependent Interaction with Ankyrin Repeat Domain 54 (ANKRD54)

Por Gustafsson, Manuela O., Hussain, Alamdar, Mohammad, Dara K., Mohamed, Abdalla J., Nguyen, Vivian, Metalnikov, Pavel, Colwill, Karen, Pawson, Tony, Smith, C. I. Edvard, Nore, Beston F.
Publicado em 2012

Ischemia-Reperfusion Injury and Pregnancy Initiate Time-Dependent and Robust Signs of Up-Regulation of Cardiac Progenitor Cells

Por Genead, Rami, Fischer, Helene, Hussain, Alamdar, Jaksch, Marie, Andersson, Agneta B., Ljung, Karin, Bulatovic, Ivana, Franco-Cereceda, Anders, Elsheikh, Elzafir, Corbascio, Matthias, Smith, C. I. Edvard, Sylvén, Christer, Grinnemo, Karl-Henrik
Publicado em 2012

Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families

Por Shafique, Sobia, Siddiqi, Saima, Schraders, Margit, Oostrik, Jaap, Ayub, Humaira, Bilal, Ammad, Ajmal, Muhammad, Seco, Celia Zazo, Strom, Tim M., Mansoor, Atika, Mazhar, Kehkashan, Shah, Syed Tahir A., Hussain, Alamdar, Azam, Maleeha, Kremer, Hannie, Qamar, Raheel
Publicado em 2014

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa

Por Azam, Maleeha, Khan, Muhammad Imran, Gal, Andreas, Hussain, Alamdar, Shah, Syed Tahir Abbas, Khan, Muhammad Shakil, Sadeque, Ahmed, Bokhari, Habib, Collin, Rob W.J., Orth, Ulrike, van Genderen, Maria M., den Hollander, A.I., Cremers, Frans P. M., Qamar, Raheel
Publicado em 2009

Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia

Por Azam, Maleeha, Collin, Rob W.J., Shah, Syed Tahir Abbas, Shah, Aftab Ali, Khan, Muhammad Imran, Hussain, Alamdar, Sadeque, Ahmed, Strom, Tim M., Thiadens, Alberta A.H.J., Roosing, Susanne, den Hollander, Anneke I., Cremers, Frans P.M., Qamar, Raheel
Publicado em 2010

Homozygosity Mapping and Targeted Sanger Sequencing Reveal Genetic Defects Underlying Inherited Retinal Disease in Families from Pakistan

Por Maria, Maleeha, Ajmal, Muhammad, Azam, Maleeha, Waheed, Nadia Khalida, Siddiqui, Sorath Noorani, Mustafa, Bilal, Ayub, Humaira, Ali, Liaqat, Ahmad, Shakeel, Micheal, Shazia, Hussain, Alamdar, Shah, Syed Tahir Abbas, Ali, Syeda Hafiza Benish, Ahmed, Waqas, Khan, Yar Muhammad, den Hollander, Anneke I., Haer-Wigman, Lonneke, Collin, Rob W. J., Khan, Muhammad Imran, Qamar, Raheel, Cremers, Frans P. M.
Publicado no PLoS One (2015)