PubMed

Production of tylosin in solid-state fermentation by Streptomyces fradiae NRRL-2702 and its gamma-irradiated mutant (gamma-1).

Khaliq S, Rashid N, Akhtar K, Ghauri MA.

Lett Appl Microbiol. 2009 Nov;49(5):635-40. Epub 2009 Aug 22.PMID: 19780953 [PubMed - in process]Related articles

RNAi as a new therapeutic strategy against HCV.

Khaliq S, Khaliq SA, Zahur M, Ijaz B, Jahan S, Ansar M, Riazuddin S, Hassan S.

Biotechnol Adv. 2009 Sep 1. [Epub ahead of print]PMID: 19729057 [PubMed - as supplied by publisher]Related articles

Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variant.

Li H, Borinskaya S, Yoshimura K, Kal'ina N, Marusin A, Stepanov VA, Qin Z, Khaliq S, Lee MY, Yang Y, Mohyuddin A, Gurwitz D, Mehdi SQ, Rogaev E, Jin L, Yankovsky NK, Kidd JR, Kidd KK.

Ann Hum Genet. 2009 May;73(Pt 3):335-45.PMID: 19456322 [PubMed - indexed for MEDLINE]Related articles

Repeated administration of fresh garlic increases memory retention in rats.

Haider S, Naz N, Khaliq S, Perveen T, Haleem DJ.

J Med Food. 2008 Dec;11(4):675-9.PMID: 19053859 [PubMed - indexed for MEDLINE]Related articles

Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene.

Lee MY, Mukherjee N, Pakstis AJ, Khaliq S, Mohyuddin A, Mehdi SQ, Speed WC, Kidd JR, Kidd KK.

Pharmacogenomics J. 2008 Oct;8(5):349-56. Epub 2008 Jul 29.PMID: 18663376 [PubMed - indexed for MEDLINE]Related articles

m-CPP induced hypolocomotion does not interfere in the assessment of memory functions in rats.

Khaliq S, Irfan B, Haider S, Haleem DJ.

Pak J Pharm Sci. 2008 Apr;21(2):139-43.PMID: 18390444 [PubMed - indexed for MEDLINE]Related articles

Fiber-optic liquid-level sensor using a long-period grating.

Khaliq S, James SW, Tatam RP.

Opt Lett. 2001 Aug 15;26(16):1224-6.PMID: 18049567 [PubMed - in process]Related articles

Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2.

Khaliq S, Abid A, White DR, Johnson CA, Ismail M, Khan A, Ayub Q, Sultana S, Maher ER, Mehdi SQ.

Am J Med Genet A. 2007 Dec 1;143A(23):2768-74.PMID: 17975799 [PubMed - indexed for MEDLINE]Related articles

A statistical model to allow the phasing out of the animal testing of demineralised bone matrix products.

Murray SS, Brochmann EJ, Harker JO, King E, Lollis RJ, Khaliq SA.

Altern Lab Anim. 2007 Aug;35(4):405-9.PMID: 17850186 [PubMed - indexed for MEDLINE]Related articles

Geographically separate increases in the frequency of the derived ADH1B*47His allele in eastern and western Asia.

Li H, Mukherjee N, Soundararajan U, Tarnok Z, Barta C, Khaliq S, Mohyuddin A, Kajuna SL, Mehdi SQ, Kidd JR, Kidd KK.

Am J Hum Genet. 2007 Oct;81(4):842-6. Epub 2007 Aug 24.PMID: 17847010 [PubMed - indexed for MEDLINE]Related articlesFree article

Change in colony morphology and kinetics of tylosin production after UV and gamma irradiation mutagenesis of Streptomyces fradiae NRRL-2702.

Khaliq S, Akhtar K, Afzal Ghauri M, Iqbal R, Mukhtar Khalid A, Muddassar M.

Microbiol Res. 2009;164(4):469-77. Epub 2007 May 2.PMID: 17475458 [PubMed - indexed for MEDLINE]Related articles

Enhanced serotonergic neurotransmission in the hippocampus following tryptophan administration improves learning acquisition and memory consolidation in rats.

Haider S, Khaliq S, Haleem DJ.

Pharmacol Rep. 2007 Jan-Feb;59(1):53-7.PMID: 17377206 [PubMed - indexed for MEDLINE]Related articlesFree article

Comparative effects of single dose and repeated oral tryptophan administration on indoleamine synthesis and memory functions in rats.

Khaliq S, Haider S, Haleem DJ.

Pak J Pharm Sci. 2007 Jan;20(1):71-6.PMID: 17337433 [PubMed - indexed for MEDLINE]Related articles

Phytochemical investigation of Perovskia abrotanoides.

Khaliq S, Volk FJ, Frahm AW.

Planta Med. 2007 Jan;73(1):77-83.PMID: 17315312 [PubMed - indexed for MEDLINE]Related articles

Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan.

Firasat S, Khaliq S, Mohyuddin A, Papaioannou M, Tyler-Smith C, Underhill PA, Ayub Q.

Eur J Hum Genet. 2007 Jan;15(1):121-6. Epub 2006 Oct 18.PMID: 17047675 [PubMed - indexed for MEDLINE]Related articlesFree article

Refinement of the locus for autosomal recessive cone-rod dystrophy (CORD8) linked to chromosome 1q23-q24 in a Pakistani family and exclusion of candidate genes.

Ismail M, Abid A, Anwar K, Mehdi SQ, Khaliq S.

J Hum Genet. 2006;51(9):827-31. Epub 2006 Aug 3.PMID: 16897189 [PubMed - indexed for MEDLINE]Related articles

Long-term tryptophan administration enhances cognitive performance and increases 5HT metabolism in the hippocampus of female rats.

Haider S, Khaliq S, Ahmed SP, Haleem DJ.

Amino Acids. 2006 Nov;31(4):421-5. Epub 2006 May 15.PMID: 16699826 [PubMed - indexed for MEDLINE]Related articles

DC-SIGN interacts with Mycobacterium leprae but sequence variation in this lectin is not associated with leprosy in the Pakistani population.

Barreiro LB, Quach H, Krahenbuhl J, Khaliq S, Mohyuddin A, Mehdi SQ, Gicquel B, Neyrolles O, Quintana-Murci L.

Hum Immunol. 2006 Jan-Feb;67(1-2):102-7. Epub 2006 Apr 5.PMID: 16698431 [PubMed - indexed for MEDLINE]Related articles

Relationship of brain tryptophan and serotonin in improving cognitive performance in rats.

Khaliq S, Haider S, Ahmed SP, Perveen T, Haleem DJ.

Pak J Pharm Sci. 2006 Jan;19(1):11-5.PMID: 16632446 [PubMed - indexed for MEDLINE]Related articles

Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases.

Abid A, Ismail M, Mehdi SQ, Khaliq S.

J Med Genet. 2006 Apr;43(4):378-81. Epub 2005 Sep 30.PMID: 16199541 [PubMed - indexed for MEDLINE]Related articlesFree article

Identification of novel TYR and TYRP1 mutations in oculocutaneous albinism.

Forshew T, Khaliq S, Tee L, Smith U, Johnson CA, Mehdi SQ, Maher ER.

Clin Genet. 2005 Aug;68(2):182-4. No abstract available. PMID: 15996218 [PubMed - indexed for MEDLINE]Related articles

Gene symbol: AIPL1. Disease: LCA4.

Khaliq S, Abid A, Hameed A, Anwar K, Mohyuddin A, Ismail M, Mehdi SQ.

Hum Genet. 2005 May;116(6):542. No abstract available. PMID: 15991325 [PubMed - indexed for MEDLINE]Related articles

Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations.

Forshew T, Johnson CA, Khaliq S, Pasha S, Willis C, Abbasi R, Tee L, Smith U, Trembath RC, Mehdi SQ, Moore AT, Maher ER.

Hum Genet. 2005 Sep;117(5):452-9. Epub 2005 Jun 16.PMID: 15959809 [PubMed - indexed for MEDLINE]Related articles

Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa.

Khaliq S, Abid A, Ismail M, Hameed A, Mohyuddin A, Lall P, Aziz A, Anwar K, Mehdi SQ.

J Med Genet. 2005 May;42(5):436-8. No abstract available. PMID: 15863674 [PubMed - indexed for MEDLINE]Related articlesFree article

Association between the angiotensin-converting enzyme gene insertion/deletion polymorphism and essential hypertension in young Pakistani patients.

Ismail M, Akhtar N, Nasir M, Firasat S, Ayub Q, Khaliq S.

J Biochem Mol Biol. 2004 Sep 30;37(5):552-5.PMID: 15479618 [PubMed - indexed for MEDLINE]Related articlesFree article

The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations.

Dharmaraj S, Leroy BP, Sohocki MM, Koenekoop RK, Perrault I, Anwar K, Khaliq S, Devi RS, Birch DG, De Pool E, Izquierdo N, Van Maldergem L, Ismail M, Payne AM, Holder GE, Bhattacharya SS, Bird AC, Kaplan J, Maumenee IH.

Arch Ophthalmol. 2004 Jul;122(7):1029-37.PMID: 15249368 [PubMed - indexed for MEDLINE]Related articlesFree article

Prevalence of Chlamydia trachomatis infection among women in a Middle Eastern community.

Ghazal-Aswad S, Badrinath P, Osman N, Abdul-Khaliq S, Mc Ilvenny S, Sidky I.

BMC Womens Health. 2004 May 27;4(1):3.PMID: 15163348 [PubMed - as supplied by publisher]Related articlesFree article

Investigation of the Greek ancestry of populations from northern Pakistan.

Mansoor A, Mazhar K, Khaliq S, Hameed A, Rehman S, Siddiqi S, Papaioannou M, Cavalli-Sforza LL, Mehdi SQ, Ayub Q.

Hum Genet. 2004 Apr;114(5):484-90. Epub 2004 Feb 25.PMID: 14986106 [PubMed - indexed for MEDLINE]Related articles

Reconstruction of human evolutionary tree using polymorphic autosomal microsatellites.

Ayub Q, Mansoor A, Ismail M, Khaliq S, Mohyuddin A, Hameed A, Mazhar K, Rehman S, Siddiqi S, Papaioannou M, Piazza A, Cavalli-Sforza LL, Mehdi SQ.

Am J Phys Anthropol. 2003 Nov;122(3):259-68.PMID: 14533184 [PubMed - indexed for MEDLINE]Related articles

Evidence of RPGRIP1 gene mutations associated with recessive cone-rod dystrophy.

Hameed A, Abid A, Aziz A, Ismail M, Mehdi SQ, Khaliq S.

J Med Genet. 2003 Aug;40(8):616-9. No abstract available. PMID: 12920076 [PubMed - indexed for MEDLINE]Related articlesFree article

Atomistic protein folding simulations on the submillisecond time scale using worldwide distributed computing.

Pande VS, Baker I, Chapman J, Elmer SP, Khaliq S, Larson SM, Rhee YM, Shirts MR, Snow CD, Sorin EJ, Zagrovic B.

Biopolymers. 2003 Jan;68(1):91-109.PMID: 12579582 [PubMed - indexed for MEDLINE]Related articles

Mutation screening of Pakistani families with congenital eye disorders.

Khaliq S, Abid A, Hameed A, Anwar K, Mohyuddin A, Azmat Z, Shami SA, Ismail M, Mehdi SQ.

Exp Eye Res. 2003 Mar;76(3):343-8.PMID: 12573663 [PubMed - indexed for MEDLINE]Related articles

HLA polymorphism in six ethnic groups from Pakistan.

Mohyuddin A, Ayub Q, Khaliq S, Mansoor A, Mazhar K, Rehman S, Mehdi SQ.

Tissue Antigens. 2002 Jun;59(6):492-501.PMID: 12445319 [PubMed - indexed for MEDLINE]Related articles

Native-like mean structure in the unfolded ensemble of small proteins.

Zagrovic B, Snow CD, Khaliq S, Shirts MR, Pande VS.

J Mol Biol. 2002 Oct 11;323(1):153-64.PMID: 12368107 [PubMed - indexed for MEDLINE]Related articles

Frequency of CCR5 Gene 32-bp deletion in Pakistani ethnic groups.

Khaliq S, Hameed A, Ayub Q, Mazhar K, Mohyuddin A, Mansoor A, Mehdi SQ.

Genet Test. 2002 Summer;6(2):123-7.PMID: 12215252 [PubMed - indexed for MEDLINE]Related articles

A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani family.

Khaliq S, Hameed A, Ismail M, Anwar K, Mehdi SQ.

Invest Ophthalmol Vis Sci. 2002 Jul;43(7):2083-7.PMID: 12091400 [PubMed - indexed for MEDLINE]Related articlesFree article

Determination of femoral artery endothelial function by phase contrast magnetic resonance imaging.

Alexander MR, Kitzman DW, Khaliq S, Darty SN, Hamilton CA, Herrington DM, Link KM, Hundley WG.

Am J Cardiol. 2001 Nov 1;88(9):1070-4. No abstract available. PMID: 11704017 [PubMed - indexed for MEDLINE]Related articles

Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreous.

Khaliq S, Hameed A, Ismail M, Anwar K, Leroy B, Payne AM, Bhattacharya SS, Mehdi SQ.

Invest Ophthalmol Vis Sci. 2001 Sep;42(10):2225-8.PMID: 11527934 [PubMed - indexed for MEDLINE]Related articlesFree article

A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family.

Hameed A, Khaliq S, Ismail M, Anwar K, Mehdi SQ, Bessant D, Payne AM, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2001 Jun;42(7):1436-8.PMID: 11381043 [PubMed - indexed for MEDLINE]Related articlesFree article

RP1 protein truncating mutations predominate at the RP1 adRP locus.

Payne A, Vithana E, Khaliq S, Hameed A, Deller J, Abu-Safieh L, Kermani S, Leroy BP, Mehdi SQ, Moore AT, Bird AC, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2000 Dec;41(13):4069-73.PMID: 11095597 [PubMed - indexed for MEDLINE]Related articlesFree article

Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24.

Khaliq S, Hameed A, Ismail M, Anwar K, Leroy BP, Mehdi SQ, Payne AM, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2000 Nov;41(12):3709-12.PMID: 11053266 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations in a new photoreceptor-pineal gene on 17p cause leber congenital amaurosis. Nat gen 2000;24:79-83

Sohoki MM, Browne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Mehdi SQ, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP.

Am J Ophthalmol. 2000 Jun;129(6):834-5. No abstract available. PMID: 10927016 [PubMed - as supplied by publisher]Related articles

P53 mutations, polymorphisms, and haplotypes in Pakistani ethnic groups and breast cancer patients.

Khaliq S, Hameed A, Khaliq T, Ayub Q, Qamar R, Mohyuddin A, Mazhar K, Qasim-Mehdi S.

Genet Test. 2000;4(1):23-9.PMID: 10794357 [PubMed - indexed for MEDLINE]Related articles

A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13.

Hameed A, Khaliq S, Ismail M, Anwar K, Ebenezer ND, Jordan T, Mehdi SQ, Payne AM, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2000 Mar;41(3):629-33.PMID: 10711674 [PubMed - indexed for MEDLINE]Related articlesFree article

HLA polymorphisms in ethnic groups from Pakistan.

Mohyuddin A, Ayub Q, Qamar R, Khaliq S, Mansoor A, Mehdi SQ.

Transplant Proc. 1999 Dec;31(8):3350-1. No abstract available. PMID: 10616502 [PubMed - indexed for MEDLINE]Related articles

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.

Sohocki MM, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP.

Nat Genet. 2000 Jan;24(1):79-83.PMID: 10615133 [PubMed - indexed for MEDLINE]Related articlesFree article

African and Levantine origins of Pakistani YAP+ Y chromosomes.

Qamar R, Ayub Q, Khaliq S, Mansoor A, Karafet T, Mehdi SQ, Hammer MF.

Hum Biol. 1999 Oct;71(5):745-55.PMID: 10510568 [PubMed - indexed for MEDLINE]Related articles

Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin.

Berry V, Mackay D, Khaliq S, Francis PJ, Hameed A, Anwar K, Mehdi SQ, Newbold RJ, Ionides A, Shiels A, Moore T, Bhattacharya SS.

Hum Genet. 1999 Jul-Aug;105(1-2):168-70.PMID: 10480374 [PubMed - indexed for MEDLINE]Related articles

Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.

Khaliq S, Hameed A, Ismail M, Mehdi SQ, Bessant DA, Payne AM, Bhattacharya SS.

Am J Hum Genet. 1999 Aug;65(2):571-4. No abstract available. PMID: 10417302 [PubMed - indexed for MEDLINE]Related articlesFree article

Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32.

Bessant DA, Anwar K, Khaliq S, Hameed A, Ismail M, Payne AM, Mehdi SQ, Bhattacharya SS.

Br J Ophthalmol. 1999 Aug;83(8):919-22.PMID: 10413693 [PubMed - indexed for MEDLINE]Related articlesFree article