Search Results - "Baig, S. M."

ACE inhibitors, angiotensin receptor blockers and endothelial injury in COVID‐19 by Tetlow, S., Segiet‐Swiecicka, A., O’Sullivan, R., O’Halloran, S., Kalb, K., Brathwaite‐Shirley, C., Alger, L., Ankuli, A., Baig, M.S., Catmur, F., Chan, T., Dudley, D., Fisher, J., Iqbal, M.U., Puczynska, J., Wilkins, R., Bygate, R., Roberts, P.

“…Background COVID‐19 is caused by the coronavirus SARS‐CoV‐2, which uses angiotensin‐converting enzyme 2 (ACE‐2) as a receptor for cellular entry. It is…”
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Identification of novel inhibitors targeting TIRAP interactions with BTK and PKCδ in inflammation through an in silico approach by Rajpoot, S., Srivastava, G., Siddiqi, M.I., Saqib, U., Parihar, S.P., Hirani, N., Baig, M.S.

“…Advanced computational tools focusing on protein-protein interaction (PPI) based drug development is a powerful platform to accelerate the therapeutic…”
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Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndrome by Lohan, S., Spielmann, M., Doelken, S.C., Flöttmann, R., Muhammad, F., Baig, S.M., Wajid, M., Hülsemann, W., Habenicht, R., Kjaer, K.W., Patil, S.J., Girisha, K.M., Abarca-Barriga, H.H., Mundlos, S., Klopocki, E.

“…Laurin‐Sandrow syndrome (LSS) is a rare autosomal dominant disorder characterized by polysyndactyly of hands and/or feet, mirror image duplication of the feet,…”
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Homozygosity for a missense variant in COMP gene associated with severe pseudoachondroplasia by Tariq, M., Khan, T.N., Lundin, L., Jameel, M., Lönnerholm, T., Baig, S.M., Dahl, N., Klar, J.

“…The phenotypic spectrum associated with heterozygous mutations in cartilage oligomeric matrix protein gene (COMP) range from a mild form of multiple epiphyseal…”
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Genetic heterogeneity in Pakistani microcephaly families by Sajid Hussain, M, Marriam Bakhtiar, S, Farooq, M, Anjum, I, Janzen, E, Reza Toliat, M, Eiberg, H, Kjaer, KW, Tommerup, N, Noegel, AA, Nürnberg, P, Baig, SM, Hansen, L

“…Autosomal recessive primary microcephaly (MCPH) is caused by mutations in at least eight different genes involved either in cell division or DNA repair. Most…”
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Cerebral involvement in benign tertian malaria by Beg, M A, Khan, R, Baig, S M, Gulzar, Z, Hussain, R, Smego, Jr, R A

“…Although Plasmodium vivax usually causes benign uncomplicated malaria, it can occasionally result in severe disease with life-threatening, end-organ…”
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Homology modeling and docking studies of Comamonas testosteroni B-356 biphenyl-2,3-dioxygenase involved in degradation of polychlorinated biphenyls by Baig, M.S., Manickam, N.

“…Biphenyl dioxygenase is a microbial enzyme which catalyzes the stereospecific dioxygenation of aromatic rings of biphenyl congeners leading to their…”
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Identifying the inhibition of TIR proteins involved in TLR signalling as an anti-inflammatory strategy by Saqib, U., Baig, M. S.

“…Toll/IL1 receptor (TIR) adaptor proteins continue to be an integral part of Toll-like receptors' (TLR) signalling involved in inflammation. Signalling is…”
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Time domain diversity combining with delay-and-advanced operation in two layered asymmetrically clipped optical OFDM system by Baig, M. S. Salman, Abas, A. F., Alresheedi, M. T., Mahdi, M. A.

“…This paper demonstrates the advantage of application of time domain diversity combining (TDDC) at the transmitter over the time domain diversity combining…”
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Prediction of viral loads for diagnosis of Hepatitis C infection in human plasma samples using Raman spectroscopy coupled with partial least squares regression analysis by Nawaz, H., Rashid, N., Saleem, M., Asif Hanif, M., Irfan Majeed, M., Amin, I., Iqbal, M., Rahman, M., Ibrahim, Ola, Baig, S. M., Ahmed, M., Bonnier, F., Byrne, H. J.

“…Raman spectroscopy has been used to identify the biochemical changes associated with the presence of the Hepatitis C virus (HCV) in infected human blood plasma…”
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Human cervicovaginal mucus contains an activity that hinders HIV-1 movement by Shukair, S A, Allen, S A, Cianci, G C, Stieh, D J, Anderson, M R, Baig, S M, Gioia, C J, Spongberg, E J, Kauffman, S M, McRaven, M D, Lakougna, H Y, Hammond, C, Kiser, P F, Hope, T J

“…Cervical and vaginal epithelia are primary barriers against HIV type I (HIV-1) entry during male-to-female transmission. Cervical mucus (CM) is produced by the…”
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Genetic heterogeneity in Pakistani microcephaly families revisited by Ahmad, I., Baig, S. M., Abdulkareem, A. R., Hussain, M. S., Sur, I., Toliat, M. R., Nürnberg, G., Dalibor, N., Moawia, A., Waseem, S. S., Asif, M., Nagra, H., Sher, M., Khan, M. M. A., Hassan, I., Rehman, S. ur, Thiele, H., Altmüller, J., Noegel, A. A., Nürnberg, P.

“…Autosomal recessive primary microcephaly (MCPH) is a rare and heterogeneous genetic disorder characterized by reduced head circumference, low cognitive prowess…”
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Ischemic Stroke subtypes in Pakistan: The Aga Khan University Stroke data bank by SYED, N. A, KHEALANI, B. A, WASAY, M, SECTION, Neurology, MEDICINE, Department Of, UNIVERSITY, The Aga, KARACHI, ALI, S, HASAN, A, AKHTAR, N, BROHI, H, MOZAFFAR, T, AHMED, N, HAMEED, A, BAIG, S. M

“…Frequency of ischemic stroke subtypes is influenced by ethnic and geographic variables. Our objective was to identify various stroke subtypes and its…”
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Probing PARP1-inhibitor complexes for the development of novel inhibitors by Saqib, U, Baig, M S

“…Poly (ADP-ribose) polymerase 1 (PARP1) is the most important member of the PARP family which has been shown to have a direct involvement in the development of…”
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Biochemical characterization of dipeptidylcarboxypeptidase of Leishmania donovani by Baig, M S, Gangwar, S, Goyal, N

“…The incidence of parasitic infection, leishmaniasis, has been steadily increasing worldwide. Since, the existing chemotherapy of these diseases suffers from…”
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Molecular and population genetic analyses of β‐Thalassemia in Turkey by Tadmouri, G.O., Tüzmen, Ş., Özçelik, H., Özer, A., Baig, S.M., Senga, E.B., Başak, A.N.

“…In this report we describe the molecular analysis of 795 chromosomes derived from unrelated Turkish β‐thalassemia and sickle cell anemia carriers identified in…”
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Cenani–Lenz syndrome restricted to limb and kidney anomalies associated with a novel LRP4 missense mutation by Khan, Tahir Naeem, Klar, J, Ali, Zafar, Khan, F, Baig, S.M, Dahl, N

“…Abstract Cenani–Lenz syndrome (CLS) is a rare autosomal recessive developmental disorder of the limbs. The disorder is characterized by complete syndactyly…”
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Identifying human disease genes: advances in molecular genetics and computational approaches by Bakhtiar, S M, Ali, A, Baig, S M, Barh, D, Miyoshi, A, Azevedo, V

“…The human genome project is one of the significant achievements that have provided detailed insight into our genetic legacy. During the last two decades,…”
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Spectrum of complications and mortality of Bacterial meningitis: an experience from a developing country by RABBANI, M. A, KHAN, A. A, ALI, S. S, AHMAD, B, BAIG, S. M, KHAN, M. A, WASAY, M

“…The aim of this study was to obtain data on predisposing factors, causative organisms and their associated mortality and complications related to acute…”
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Anti-purified protein derivative cell-enzyme-linked immunosorbent assay, a sensitive method for early diagnosis of tuberculous meningitis by Baig, S M

“…Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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