Shah ST - Search Results

1

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.

Azam M, Khan MI, Gal A, Hussain A, Shah ST, Khan MS, Sadeque A, Bokhari H, Collin RW, Orth U, van Genderen MM, den Hollander AI, Cremers FP, Qamar R. Azam M, et al. Among authors: shah st. Mol Vis. 2009 Dec 3;15:2526-34. Mol Vis. 2009. PMID: 19960070 Free PMC article.

2

A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.

Azam M, Collin RW, Khan MI, Shah ST, Qureshi N, Ajmal M, den Hollander AI, Qamar R, Cremers FP. Azam M, et al. Among authors: shah st. Mol Vis. 2009 Sep 5;15:1788-93. Mol Vis. 2009. PMID: 19753316 Free PMC article.

3

Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia.

Azam M, Collin RW, Shah ST, Shah AA, Khan MI, Hussain A, Sadeque A, Strom TM, Thiadens AA, Roosing S, den Hollander AI, Cremers FP, Qamar R. Azam M, et al. Among authors: shah st, shah aa. Mol Vis. 2010 Apr 29;16:774-81. Mol Vis. 2010. PMID: 20454696 Free PMC article.

4

Toxic metals signature in the human seminal plasma of Pakistani population and their potential role in male infertility.

Zafar A, Eqani SA, Bostan N, Cincinelli A, Tahir F, Shah ST, Hussain A, Alamdar A, Huang Q, Peng S, Shen H. Zafar A, et al. Among authors: shah st. Environ Geochem Health. 2015 Jun;37(3):515-27. doi: 10.1007/s10653-014-9666-8. Epub 2014 Dec 4. Environ Geochem Health. 2015. PMID: 25471479

5

Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.

Maria M, Ajmal M, Azam M, Waheed NK, Siddiqui SN, Mustafa B, Ayub H, Ali L, Ahmad S, Micheal S, Hussain A, Shah ST, Ali SH, Ahmed W, Khan YM, den Hollander AI, Haer-Wigman L, Collin RW, Khan MI, Qamar R, Cremers FP. Maria M, et al. Among authors: shah st. PLoS One. 2015 Mar 16;10(3):e0119806. doi: 10.1371/journal.pone.0119806. eCollection 2015. PLoS One. 2015. PMID: 25775262 Free PMC article.

6

Increased expression levels of Syntaxin 1A and Synaptobrevin 2/Vesicle-Associated Membrane Protein-2 are associated with the progression of bladder cancer.

Raja SA, Abbas S, Shah STA, Tariq A, Bibi N, Yousuf A, Khawaja A, Nawaz M, Mehmood A, Khan MJ, Hussain A. Raja SA, et al. Genet Mol Biol. 2019 Jan-Mar;42(1):40-47. doi: 10.1590/1678-4685-GMB-2017-0339. Epub 2019 Jan 21. Genet Mol Biol. 2019. PMID: 30672978 Free PMC article.

7

Caveolin-1 and dynamin-2 overexpression is associated with the progression of bladder cancer.

Raja SA, Shah STA, Tariq A, Bibi N, Sughra K, Yousuf A, Khawaja A, Nawaz M, Mehmood A, Khan MJ, Hussain A. Raja SA, et al. Oncol Lett. 2019 Jul;18(1):219-226. doi: 10.3892/ol.2019.10310. Epub 2019 May 3. Oncol Lett. 2019. PMID: 31289491 Free PMC article.

8

Environmental exposure pathway analysis of trace elements and autism risk in Pakistani children population.

Nabgha-E-Amen, Eqani SAMAS, Khuram F, Alamdar A, Tahir A, Shah STA, Nasir A, Javed S, Bibi N, Hussain A, Rasheed H, Shen H. Nabgha-E-Amen, et al. Sci Total Environ. 2020 Apr 10;712:136471. doi: 10.1016/j.scitotenv.2019.136471. Epub 2020 Jan 7. Sci Total Environ. 2020. PMID: 31927446

9

Effect of gasotransmitters treatment on expression of hypertension, vascular and cardiac remodeling and hypertensive nephropathy genes in left ventricular hypertrophy.

Ahmad A, Riaz Z, Sattar MA, Khan SA, John EJ, Rashid S, Shah STA, Rafiq MA, Azam M, Qamar R. Ahmad A, et al. Gene. 2020 May 5;737:144479. doi: 10.1016/j.gene.2020.144479. Epub 2020 Feb 14. Gene. 2020. PMID: 32068124

10

Association analysis of single nucleotide polymorphisms in autophagy related 7 (ATG7) gene in patients with coronary artery disease.

Sarosh M, Nurulain SM, Shah STA, Jadoon Khan M, Muneer Z, Bibi N, Shah SFA, Hussain S. Sarosh M, et al. Medicine (Baltimore). 2022 Jul 1;101(26):e29776. doi: 10.1097/MD.0000000000029776. Medicine (Baltimore). 2022. PMID: 35777002 Free PMC article.

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