Ajmal M - Search Results

1

Decreased serum PON1 arylesterase activity in familial hypercholesterolemia patients with a mutated LDLR gene.

Idrees M, Siddiq AR, Ajmal M, Akram M, Khalid RR, Hussain A, Qamar R, Bokhari H. Idrees M, et al. Among authors: ajmal m. Genet Mol Biol. 2018 Jul/Sept.;41(3):570-577. doi: 10.1590/1678-4685-GMB-2016-0287. Epub 2018 Jul 23. Genet Mol Biol. 2018. PMID: 30044465 Free PMC article.

2

Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia.

Ajmal M, Ahmed W, Sadeque A, Ali SH, Bokhari SH, Ahmed N, Qamar R. Ajmal M, et al. Mol Biol Rep. 2010 Dec;37(8):3869-75. doi: 10.1007/s11033-010-0043-0. Epub 2010 Mar 10. Mol Biol Rep. 2010. PMID: 20217239

3

Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patients.

Ahmed W, Ajmal M, Sadeque A, Whittall RA, Rafiq S, Putt W, Khawaja A, Imtiaz F, Ahmed N, Azam M, Humphries SE, Qamar R. Ahmed W, et al. Among authors: ajmal m. Mol Biol Rep. 2012 Jul;39(7):7365-72. doi: 10.1007/s11033-012-1568-1. Epub 2012 Feb 7. Mol Biol Rep. 2012. PMID: 22311046

4

Role of tissue plasminogen activator and plasminogen activator inhibitor polymorphism in myocardial infarction.

Ahmed W, Malik M, Saeed I, Khan AA, Sadeque A, Kaleem U, Ahmed N, Ajmal M, Azam M, Qamar R. Ahmed W, et al. Among authors: ajmal m. Mol Biol Rep. 2011 Apr;38(4):2541-8. doi: 10.1007/s11033-010-0392-8. Epub 2010 Nov 17. Mol Biol Rep. 2011. PMID: 21082259

5

A novel pathogenic nonsense triple-nucleotide mutation in the low-density lipoprotein receptor gene and its clinical correlation with familial hypercholesterolemia.

Ajmal M, Ahmed W, Akhtar N, Sadeque A, Khalid A, Benish Ali SH, Ahmed N, Azam M, Qamar R. Ajmal M, et al. Genet Test Mol Biomarkers. 2011 Sep;15(9):601-6. doi: 10.1089/gtmb.2010.0184. Epub 2011 Apr 3. Genet Test Mol Biomarkers. 2011. PMID: 21457052

6

The genetic spectrum of familial hypercholesterolemia in Pakistan.

Ahmed W, Whittall R, Riaz M, Ajmal M, Sadeque A, Ayub H, Qamar R, Humphries SE. Ahmed W, et al. Among authors: ajmal m. Clin Chim Acta. 2013 Jun 5;421:219-25. doi: 10.1016/j.cca.2013.03.017. Epub 2013 Mar 25. Clin Chim Acta. 2013. PMID: 23535506 Free PMC article.

7

Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosa.

Ajmal M, Khan MI, Micheal S, Ahmed W, Shah A, Venselaar H, Bokhari H, Azam A, Waheed NK, Collin RW, den Hollander AI, Qamar R, Cremers FP. Ajmal M, et al. Mol Vis. 2012;18:1226-37. Epub 2012 May 10. Mol Vis. 2012. PMID: 22665969 Free PMC article.

8

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: ajmal m. Mol Vis. 2009 Sep 5;15:1788-93. Mol Vis. 2009. PMID: 19753316 Free PMC article.

9

Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts.

Ayub H, Khan MI, Micheal S, Akhtar F, Ajmal M, Shafique S, Ali SH, den Hollander AI, Ahmed A, Qamar R. Ayub H, et al. Among authors: ajmal m. Mol Vis. 2010 Jan 11;16:18-25. Mol Vis. 2010. PMID: 20069064 Free PMC article.

10

A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular coloboma.

Ajmal M, Khan MI, Neveling K, Khan YM, Azam M, Waheed NK, Hamel CP, Ben-Yosef T, De Baere E, Koenekoop RK, Collin RW, Qamar R, Cremers FP. Ajmal M, et al. J Med Genet. 2014 Jul;51(7):444-8. doi: 10.1136/jmedgenet-2014-102316. Epub 2014 Apr 15. J Med Genet. 2014. PMID: 24737827

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