Zobrazeno 1 - 10
of 38
pro vyhledávání: '"S. Q. Mehdi"'
Autor:
D. M. Walsh, S. H. Shah, M. A. Simpson, N. V. Morgan, S. Khaliq, R. C. Trembath, S. Q. Mehdi, E. R. Maher
Publikováno v:
Scientifica, Vol 2012 (2012)
Autosomal recessive congenital ichthyosis (ARCI) is a rare genetically heterogeneous disorder characterized by hyperkeratosis in addition to dry, scaly skin. There are six genes currently known to be associated with the disease. Exome sequencing data
Externí odkaz:
https://doaj.org/article/7861d82f08e9480484f8360783d98a35
Autor:
Aisha Mohyuddin, Kenneth K. Kidd, William C. Speed, Shagufta Khaliq, S Q Mehdi, M-Y Lee, A.J. Pakstis, Namita Mukherjee, J.R. Kidd
Publikováno v:
The Pharmacogenomics Journal. 8:349-356
Cytochrome P450 2E1, gene symbol CYP2E1, is one of a family of enzymes with a central role in activating and detoxifying xenobiotics and endogenous compounds. Genetic variation at this gene has been reported in different human populations, and some a
Autor:
S. Q. Mehdi, A. Mohyuddin
Publikováno v:
Tissue Antigens. 66:691-695
The Parsis of Pakistan are descendants of Zoroastrians from Iran who fled to Gujarat in India after the Arab invasion in 900 AD. A small group eventually migrated from India to Karachi in Pakistan. In this study, the Parsis from Pakistan were analyze
Publikováno v:
Clinical Genetics. 68:182-184
Autor:
S. Q. Mehdi, Eamonn R. Maher, Shagufta Khaliq, Neil V. Morgan, S. H. Shah, Diana Walsh, Richard C. Trembath, Michael A. Simpson
Publikováno v:
Scientifica
Scientifica, Vol 2012 (2012)
Scientifica, Vol 2012 (2012)
Autosomal recessive congenital ichthyosis (ARCI) is a rare genetically heterogeneous disorder characterized by hyperkeratosis in addition to dry, scaly skin. There are six genes currently known to be associated with the disease. Exome sequencing data
Autor:
F. Ramos, S. Q. Mehdi, Fernando Tobias Silveira, Shannon Atkinson, F. Kaukab, Hazel M. Dockrell, Marie-Anne Shaw, Jenefer M. Blackwell, Z. Lins-Lainson, Rabia Hussain, J. J. Shaw, S. A. Khaliq, T. Chiang
Publikováno v:
Scopus-Elsevier
The mycobacterial diseases leprosy and tuberculosis (TB) and the leishmaniases are characterized by a wide spectrum of disease phenotypes, and by the fact that the majority of individuals exposed to the causative organisms Mycobacterium leprae, M. tu
Publikováno v:
Aggressive behavior. 35(1)
Studies show that personality dimensions such as aggression are influenced by genetic factors and that allelic variants located on the Y chromosome influence such behavior. We investigated polymorphisms on the male-specific region of the human Y chro
Autor:
George M. Hahn, S. Q. Mehdi
Publikováno v:
International Journal of Hyperthermia. 6:553-561
The effect of hyperthermia, fractionated heat and the synthesis of heat shock proteins on the lateral diffusion of H-2Kk was examined in RDM-4, Ch-1 and mouse L cells. Cells in suspension were examined immediately after heating, adaptation to growth
Autor:
N S Enattah, A Trudeau, V Pimenoff, L Maiuri, S Auricchio, L Creco, M Rossi, M Lentze, J K Seo, S Rahgozar, I Khalil, M Alifrangis, S Natah, L Groop, N Shaat, A Kozlov, G Verschubskaya, D Comas, K Bulaeva, S Q Mehdi, J D Terwilliger, T Sahi, E Savilahti
Publikováno v:
American journal of human genetics 81(3) (2007): 615–625.
info:cnr-pdr/source/autori:N S Enattah, A Trudeau, V Pimenoff, L Maiuri, S Auricchio, L Creco, M Rossi, M Lentze, J K Seo, S Rahgozar, I Khalil, M Alifrangis, S Natah, L Groop, N Shaat, A Kozlov, G Verschubskaya, D Comas, K Bulaeva, S Q Mehdi, J D Terwilliger, T Sahi, E Savilahti,/titolo:Evidence for still ongoing convergence evolution of the lactase persistence T-13910 alleles in humans/doi:/rivista:American journal of human genetics/anno:2007/pagina_da:615/pagina_a:625/intervallo_pagine:615–625/volume:81(3)
info:cnr-pdr/source/autori:N S Enattah, A Trudeau, V Pimenoff, L Maiuri, S Auricchio, L Creco, M Rossi, M Lentze, J K Seo, S Rahgozar, I Khalil, M Alifrangis, S Natah, L Groop, N Shaat, A Kozlov, G Verschubskaya, D Comas, K Bulaeva, S Q Mehdi, J D Terwilliger, T Sahi, E Savilahti,/titolo:Evidence for still ongoing convergence evolution of the lactase persistence T-13910 alleles in humans/doi:/rivista:American journal of human genetics/anno:2007/pagina_da:615/pagina_a:625/intervallo_pagine:615–625/volume:81(3)
A single nucleotide variant, C/T-13910, located 14 kb upstream from the lactase (LCT) gene has been shown to be completely correlated with lactase persistence (LP) in Northern Europeans. Here we analysed the allelic background of the alleles carrying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::e67847f35957e4f0faf664c236ff1809
https://publications.cnr.it/doc/45801
https://publications.cnr.it/doc/45801
Publikováno v:
Tissue antigens. 61(4)
The extreme polymorphism found at some loci of the HLA system has made it an invaluable tool for population genetic analyses. In this study eight diverse ethnic groups from Pakistan were analyzed at the HLA-A locus using sequence specific primers for