1. 158 ANTENATAL INDOMETHACIN SUPPRESSES LUNG MATRIX METALLOPROTEINASE ACTIVITY AND VASCULAR ENDOTHELIAL GROWTH FACTOR LEVELS IN FETAL RABBITS. (1st January 2006) Authors: Gharraee, Z.; Beharry, K. D.; Fortson, W.; Hasan, J.; Jan, A.; Abad-Santos, P.; Sills, J. H.; Valencia, A. M.; Modanlou, H. D. Journal: Journal of investigative medicine Issue: Volume 54:Number 1(2006) Page Start: S107 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 467 EFFECT OF INDOMETHACIN AND IBUPROFEN ON RAT LUNG VASCULAR ENDOTHELIAL GROWTH FACTOR AND SOLUBLE VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTORS DURING EARLY POSTNATAL DEVELOPMENT. (1st January 2006) Authors: Gharraee, Z.; Beharry, K. D.; Hasan, J.; Abad-Santos, P.; Jan, A.; Sills, J. H.; Aranda, J. V.; Modanlou, H. D. Journal: Journal of investigative medicine Issue: Volume 54:Number 1(2006) Page Start: S159 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel deletion mutation in the DSG4 gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families. (1st January 2015) Authors: Ullah, A.; Raza, S. I.; Ali, R. H.; Naveed, A. K.; Jan, A.; Rizvi, S. D. A.; Satti, R.; Ahmad, W. Journal: Clinical and experimental dermatology Issue: Volume 40:Number 1(2015) Page Start: 78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A novel deletion mutation in the DSG4 gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families. (23rd September 2014) Authors: Ullah, A.; Raza, S. I.; Ali, R. H.; Naveed, A. K.; Jan, A.; Rizvi, S. D. A.; Satti, R.; Ahmad, W. Journal: Clinical and experimental dermatology Issue: Volume 40:Number 1(2015) Page Start: 78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Efficiency of thermal outgassing for tritium retention measurement and removal in ITER. (August 2017) Authors: De Temmerman, G.; Baldwin, M.J.; Anthoine, D.; Heinola, K.; Jan, A.; Jepu, I.; Likonen, J.; Lungu, C.P.; Porosnicu, C.; Pitts, R.A. Journal: Nuclear materials and energy Issue: Volume 12(2017) Page Start: 267 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Frequency and antimicrobial sensitivity of Escherichia coli 0157:h7 in healthy farm/abattoir/poultry workers of Peshawar, Pakistan. (August 2018) Authors: Jan, A. Journal: International journal of infectious diseases Issue: Volume 73(2018)Supplement Page Start: 393 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Homozygous SLCO2A1 translation initiation codon mutation in a Pakistani family with recessive isolated congenital nail clubbing. (1st August 2017) Authors: Shah, K.; Ferrara, T.M.; Jan, A.; Umair, M.; Irfanullah, ; Khan, S.; Ahmad, W.; Spritz, R.A. Journal: British journal of dermatology Issue: Volume 177:Number 2(2017) Page Start: 546 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Homozygous SLCO2A1 translation initiation codon mutation in a Pakistani family with recessive isolated congenital nail clubbing. (22nd June 2017) Authors: Shah, K.; Ferrara, T.M.; Jan, A.; Umair, M.; Irfanullah, ; Khan, S.; Ahmad, W.; Spritz, R.A. Journal: British journal of dermatology Issue: Volume 177:Number 2(2017) Page Start: 546 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families. (23rd May 2018) Authors: Ahmad, F.; Shah, K.; Umair, M.; Jan, A.; Irfanullah, ; Khan, S.; Muhammad, D.; Basit, S.; Wakil, S. M.; Ramzan, K.; Ahmad, W. Journal: Clinical and experimental dermatology Issue: Volume 43:Number 6(2018) Page Start: 752 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families. (1st August 2018) Authors: Ahmad, F.; Shah, K.; Umair, M.; Jan, A.; Irfanullah, ; Khan, S.; Muhammad, D.; Basit, S.; Wakil, S. M.; Ramzan, K.; Ahmad, W. Journal: Clinical and experimental dermatology Issue: Volume 43:Number 6(2018) Page Start: 752 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗