Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jamila Iqbal"'
Autor:
Melissa A. Nehls, Jamila Iqbal Ranavaya, Sydney Smith-Graham, Micah Ray, Aryana Misaghi, Jennie Yoost, Kelly Cummings
Publikováno v:
Marshall Journal of Medicine, Vol 8, Iss 3 (2022)
In recent times, there has been an increase in drug abuse in not only the general population, but in women of reproductive age. Our objectives were to identify, classify, and describe the spectrum of complications, the average number of admissions, a
Externí odkaz:
https://doaj.org/article/fbd15fe74d4a486e8a76fcb485c7fa1a
Autor:
Laura M. Rantanen, Maina Bitar, Riikka Lampinen, Romal Stewart, Hazel Quek, Lotta E. Oikari, Carla Cunί-Lόpez, Ratneswary Sutharsan, Gayathri Thillaiyampalam, Jamila Iqbal, Daniel Russell, Elina Penttilä, Heikki Löppönen, Juha-Matti Lehtola, Toni Saari, Sanna Hannonen, Anne M. Koivisto, Larisa M. Haupt, Alan Mackay-Sim, Alexandre S. Cristino, Katja M. Kanninen, Anthony R. White
Publikováno v:
Cells, Vol 11, Iss 20, p 3258 (2022)
An early symptom of Alzheimer’s disease (AD) is an impaired sense of smell, for which the molecular basis remains elusive. Here, we generated human olfactory neurosphere-derived (ONS) cells from people with AD and mild cognitive impairment (MCI), a
Externí odkaz:
https://doaj.org/article/dca05e7e61d14b3aa34487459c0f0668
Autor:
Steven R. Bentley, Suliman Khan, Marco Öchsner, Susitha Premarathne, Zain Aslam, Javed Y. Fowdar, Jamila Iqbal, Muhammad Naeem, Christopher A. Love, Stephen A. Wood, George D. Mellick, Alex M. Sykes
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
The study of consanguineous families has provided novel insights into genetic causes of monogenic parkinsonism. Here, we present a family from the rural Khyber Pakhtunkhwa province, Pakistan, where three siblings were diagnosed with early-onset parki
Externí odkaz:
https://doaj.org/article/5a51418bc4344b788a604a11a65095cc
Autor:
William Gang Miao, Thanh Nguyen, Jamila Iqbal, Gregory K. Pierens, Linlin Ma, Des R. Richardson, Stephen A. Wood, George D. Mellick, Ronald J. Quinn, Yunjiang Feng
Publikováno v:
ACS Chemical Neuroscience. 13:2565-2578
Autor:
Laura M. Rantanen, Maina Bitar, Riikka Lampinen, Romal Stewart, Hazel Quek, Lotta E. Oikari, Carla Cunί-Lόpez, Ratneswary Sutharsan, Gayathri Thillaiyampalam, Jamila Iqbal, Daniel Russell, Elina Penttilä, Heikki Löppönen, Juha-Matti Lehtola, Toni Saari, Sanna Hannonen, Anne M Koivisto, Larisa M. Haupt, Alan Mackay-Sim, Alexandre S. Cristino, Katja M. Kanninen, Anthony R. White
An early symptom of Alzheimer’s disease (AD) is an impaired sense of smell, for which the molecular basis remains elusive. Here, we generated human olfactory neurosphere-derived (ONS) cells from people with AD and mild cognitive impairment (MCI), a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::354e428e616eaf06921774d3cad236a1
https://doi.org/10.1101/2022.08.22.504884
https://doi.org/10.1101/2022.08.22.504884
Autor:
Jianying Han, Jamila Iqbal, Duy Thanh Nguyen, Stephen A. Wood, George D. Mellick, Yunjiang Feng, Gregory K. Pierens
Publikováno v:
Bioorganicmedicinal chemistry. 28(21)
Cytological profiling (CP) assay against a human olfactory neuroshpere-derived (hONS) cell line using a library of traditional Chinese medicinal plant extracts gave indications that the ethanolic extract of Macleaya cordata (Willd) R. Br. elicited st
Autor:
Christopher Love, George D. Mellick, Susitha Premarathne, Javed Fowdar, Zain Aslam, Alex M. Sykes, Jamila Iqbal, Marco Öchsner, Stephen A. Wood, Steven R. Bentley, Muhammad Naeem, Suliman Khan
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Frontiers in Neurology
Frontiers in Neurology
The study of consanguineous families has provided novel insights into genetic causes of monogenic parkinsonism. Here, we present a family from the rural Khyber Pakhtunkhwa province, Pakistan, where three siblings were diagnosed with early-onset parki
Autor:
Giulia Venturini, Sundus Sajid, Muhammad Ansar, Afeefa Jarral, Carlo Rivolta, Konstantinos Nikopoulos, Rabia Bibi, Ehsan Ullah, Jamila Iqbal, Koji M. Nishiguchi, Muhammad Arif Nadeem Saqib, Falak Sher Khan
Publikováno v:
Scientific Reports, vol. 5, pp. 9965
Scientific Reports
Scientific Reports
Inherited retinal dystrophies are phenotypically and genetically heterogeneous. This extensive heterogeneity poses a challenge when performing molecular diagnosis of patients, especially in developing countries. In this study, we applied homozygosity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7ee7f3cd871a84cebcc1414f5070228
https://edoc.unibas.ch/81715/
https://edoc.unibas.ch/81715/