Instant nano-hydroxyapatite: a continuous and rapid hydrothermal synthesis (2006)
Chaudhry, A.A., Haque, S., Kellici, S., Boldrin, P., Rehman, I., Khalid, F.A., ...
Nano-particle hydroxyapatite (HA) rods, were rapidly synthesised using a three pump continuous hydrothermal process (using a water feed at up to 400 °C and at 24 MPa): the product was obtained as a...
Interfacial electron transfer in dye sensitized TiO2 photoelectrochemical solar cells (2006)
Durrant, J. R., Tachibana, Y., Haque, S., Klug, D. R., Moser, J. E., Gratzel, M.
S. Srinivasan, D.P. Mital, S. Haque
This study reports the design and successful implementation of a decision support system for use by a multi-purpose health worker or in any situation where there is no immediate pediatric or neonatal...
Zaidi, SH, King, LM, Haque, S, Patel, M, Ahmad, M, ...
Split-hand/split-foot malformation (SHFM) is a genetically heterogeneous disorder, with five known loci, that causes a lack of median digital rays, syndactyly, and aplasia or hypoplasia of the...
A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1 (2005)
Rafiq, MA, Ud, Din, Malik, S, Sohail, M, Anwar, M, ...
Ectodermal dysplasia (ED) represents a heterogeneous group of genetic disorders characterized by the absence or deformity in two or more of the ectodermal appendages. We have studied an autosomal...
Ahmad, W, Zaidi, SHE, Hussain, SS, Haque, S, Cohn, DH, ...
Multiple hereditary exostoses (HME) is an autosomal dominant developmental disorder exhibiting multiple osteocartilaginous bone tumors that generally arise near the ends of growing long bones. Here,...
Ahmad, W, Zaidi, SHE, Haque, S, Teebi, AS, Ahmad, M, ...
The present authors have previously described a consanguineous Pakistani family with fibular hypoplasia and complex brachydactyly (DuPan syndrome) inherited as an autosomal recessive trait. All...
Ahmad, W, Wahab, A, Haque, S, Azim, AC, Zaidi, SHE, ...
Grebe-type chondrodysplasia exhibits a severe form of limb shortening and appendicular bone dysmorphogenesis. Here we report a family with seven males and six females who inherited the disorder in an...
Some advances in the theory of succesive over-relaxation. (1980)
Thesis (Ph. D.)--University of Aberdeen, 1980.
Some advances in the theory of successive over-relaxation. (1980)
Haque, S, Aberdeen Univ. (GB).
Thesis (Ph.D.)
A Toxoplasma gondii-derived factor(s) stimulates immune downregulation: an in vitro model.
Haque, S, Haque, A, Kasper, L H
Suppression of the T-cell lymphoproliferative response and downregulation of interleukin 2 (IL-2) production by Toxoplasma gondii has been observed following in vivo infection. In this study, an...
Identification of murine protective epitopes on the Porphyromonas gingivalis fimbrillin molecule.
Deslauriers, M, Haque, S, Flood, P M
Fimbriae from Porphyromonas gingivalis are believed to play an important role in the pathogenesis of periodontal diseases. The aim of the present study was to identify the fimbrial protective T-cell...
Washington, O R, Deslauriers, M, Stevens, D P, Lyford, L K, Haque, S, Yan, Y, ...
Fimbrillin is the major subunit protein of fimbriae from the human periodontal pathogen Porphyromonas (Bacteroides) gingivalis. We describe here the generation and initial characterization of...
Haque, S, Khan, I, Haque, A, Kasper, L
Depression of the cellular immune response to Toxoplasma gondii has been reported in both mice and humans. The present study was undertaken to determine the kinetics and mechanism of the observed...
A gene for universal congenital alopecia maps to chromosome 8p21-22.
Nöthen, M M, Cichon, S, Vogt, I R, Hemmer, S, Kruse, R, Knapp, M, ...
Complete or partial congenital absence of hair (congenital alopecia) may occur either in isolation or with associated defects. The majority of families with isolated congenital alopecia has been...
A Toxoplasma gondii-derived factor(s) stimulates immune downregulation: an in vitro model.
Haque, S, Haque, A, Kasper, L H
Suppression of the T-cell lymphoproliferative response and downregulation of interleukin 2 (IL-2) production by Toxoplasma gondii has been observed following in vivo infection. In this study, an...
Identification of murine protective epitopes on the Porphyromonas gingivalis fimbrillin molecule.
Deslauriers, M, Haque, S, Flood, P M
Fimbriae from Porphyromonas gingivalis are believed to play an important role in the pathogenesis of periodontal diseases. The aim of the present study was to identify the fimbrial protective T-cell...
Washington, O R, Deslauriers, M, Stevens, D P, Lyford, L K, Haque, S, Yan, Y, ...
Fimbrillin is the major subunit protein of fimbriae from the human periodontal pathogen Porphyromonas (Bacteroides) gingivalis. We describe here the generation and initial characterization of...
Haque, S, Khan, I, Haque, A, Kasper, L
Depression of the cellular immune response to Toxoplasma gondii has been reported in both mice and humans. The present study was undertaken to determine the kinetics and mechanism of the observed...
A gene for universal congenital alopecia maps to chromosome 8p21-22.
Nöthen, M M, Cichon, S, Vogt, I R, Hemmer, S, Kruse, R, Knapp, M, ...
Complete or partial congenital absence of hair (congenital alopecia) may occur either in isolation or with associated defects. The majority of families with isolated congenital alopecia has been...
Haque, A, Chamekh, M, Cornelis, J, Capron, A, Haque, S
In order to elucidate the relationship between the structure and function of proteins encoded for by the Ly-6 gene complex, a cDNA was constructed for a Ly-6.2 specificity and then monoclonal...
HAQUE, A, RACHINEL, N, QUDDUS, M R, HAQUE, S, KASPER, L H, USHERWOOD, E
In order to study the interaction between a γ-herpesvirus and malaria we established a co-infection model that involves infection of mice with murine γ-herpesvirus (MHV-68) and Plasmodium yoelii...