THE EFFECT OF HEXOESTROL ON CALCIUM METABOLISM IN THE SHEEP = EFFET DE L'HEXOESTROL SUR LE METABOLISME DE CA CHEZ LE MOUTONBRAITHWAITE GD; GLASCOCK RF; RIAZUDDIN S et al.1972; BRIT. J. NUTRIT.; G.B.; DA. 1972; VOL. 28; NO 2; PP. 269-273; BIBL. 20REF.Article

The molecular genetics of Usher syndromeAHMED, Z. M; RIAZUDDIN, S; RIAZUDDIN, S et al.RIAZUDDIN, S; RIAZUDDIN, S et al.Clinical genetics. 2003, Vol 63, Num 6, pp 431-444, issn 0009-9163, 14 p.Article

New approaches to generate disease-resistant GladiolusIDREES AHMAD NASIR; RIAZUDDIN, S.World journal of microbiology & biotechnology. 2008, Vol 24, Num 3, pp 367-373, issn 0959-3993, 7 p.Article

Strain and cultivar specificity in the Agrobacterium-chickpea interactionISLAM, R; MALIK, T; HUSNAIN, T et al.Plant cell reports (Print). 1994, Vol 13, Num 10, pp 561-563, issn 0721-7714Article

Determination of receptor binding properties of Bacillus thuringiensis δ-endotoxins to cotton bollworm (Helicoverpa zea) and pink bollworm (Pectinophora gossypiella) midgut brush border membrane vesiclesKARIM, S; RIAZUDDIN, S; GOULD, F et al.Pesticide biochemistry and physiology (Print). 2000, Vol 67, Num 3, pp 198-216, issn 0048-3575Article

Methyl transferases induced during chemical adaptation of M. luteusRIAZUDDIN, S; ATHAR, A; SOHAIL, A et al.Nucleic acids research. 1987, Vol 15, Num 22, pp 9471-9486, issn 0305-1048Article

Mutagenicity testing of some medicinal herbsRIAZUDDIN, S; MALIK, M. M; NASIM, A et al.Environmental and molecular mutagenesis (Print). 1987, Vol 10, Num 2, pp 141-148, issn 0893-6692Article

DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3ALI, R. A; REHMAN, A. U; KHAN, S. N et al.Clinical genetics. 2012, Vol 81, Num 5, pp 498-500, issn 0009-9163, 3 p.Article

The myth of plant transformationABDUL QAYYUM RAO; BAKHSH, Allah; KIANI, Sarfraz et al.Biotechnology advances. 2009, Vol 27, Num 6, pp 753-763, issn 0734-9750, 11 p.Article

DNA glycosylase enzymes induced during chemical adaptation of M. luteusRIAZUDDIN, S; ATHAR, A; AHMED, Z et al.Nucleic acids research. 1987, Vol 15, Num 16, pp 6607-6624, issn 0305-1048Article

Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in PakistanCHOI, B. Y; AHMED, Z. M; RIAZUDDIN, S et al.RIAZUDDIN, S et al.Clinical genetics. 2009, Vol 75, Num 3, pp 237-243, issn 0009-9163, 7 p.Article

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunctionNAZ, S; GRIFFITH, A. J; RIAZUDDIN, S et al.Journal of medical genetics. 2004, Vol 41, Num 8, pp 591-595, issn 0022-2593, 5 p.Article

Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in PakistanKITAJIRI, S.-I; MCNAMARA, R; MAKISHIMA, T et al.Clinical genetics. 2007, Vol 72, Num 6, pp 546-550, issn 0009-9163, 5 p.Article

Distinctive audiometric profile associated with DFNB21 alleles of TECTANAZ, S; ALASTI, F; MOWJOODI, A et al.Journal of medical genetics. 2003, Vol 40, Num 5, pp 360-363, issn 0022-2593, 4 p.Article

Production of the phytotoxins, solanapyrones A and C and cytochalasin D among nine isolates of Ascochyta rabieiLATIF, Z; STRANGE, R. N; BILTON, J et al.Plant pathology. 1993, Vol 42, Num 2, pp 172-180, issn 0032-0862Article

Adaptive response of Micrococcus luteus to alkylating chemicalsATHER, A; AHMED, Z; RIAZUDDIN, S et al.Nucleic acids research. 1984, Vol 12, Num 4, pp 2111-2126, issn 0305-1048Article

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15WARYAH, A. M; REHMAN, A; AHMED, Z. M et al.Clinical genetics. 2009, Vol 76, Num 3, pp 270-275, issn 0009-9163, 6 p.Article

USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23AHMED, Z. M; RIAZUDDIN, S; KHAN, S. N et al.RIAZUDDIN, S; Clinical genetics. 2009, Vol 75, Num 1, pp 86-91, issn 0009-9163, 6 p.Article

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessPARK, H.-J; SHAUKAT, S; RIAZUDDIN, S et al.Journal of medical genetics. 2003, Vol 40, Num 4, pp 242-248, issn 0022-2593, 7 p.Article

CDH23 mutation and phenotype heterogeneity: A profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessASTUTO, L. M; BORK, J. M; KREMER, H et al.American journal of human genetics. 2002, Vol 71, Num 2, pp 262-275, issn 0002-9297Article

Variability in expression of insecticidal Cry1Ab gene in Indica Basmati riceHUSNAIN, Tayyab; ASAD, Jan; MAQBOOL, Shahina B et al.Euphytica. 2002, Vol 128, Num 1, pp 121-128, issn 0014-2336, 8 p.Article

Studies on the expression of marker genes in chickpeaHUSNAIN, T; MALIK, T; RIAZUDDIN, S et al.Plant cell, tissue and organ culture. 1997, Vol 49, Num 1, pp 7-16, issn 0167-6857Article

Linkage of a Mild Late-Onset Phenotype of Fuchs Corneal Dystrophy to a Novel Locus at 5q33.1-q35.2AMER RIAZUDDIN, S; EGHRARI, Allen O; AL-SAIF, Amr et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 12, pp 5667-5671, issn 0146-0404, 5 p.Article

A Novel Locus for Autosomal Recessive Retinitis Pigmentosa in a Consanguineous Pakistani Family Maps to Chromosome 2pNAZ, Shagufta; AMER RIAZUDDIN, S; LIN LI et al.American journal of ophthalmology. 2010, Vol 149, Num 5, pp 861-866, issn 0002-9394, 6 p.Article

Progression of Fuchs Corneal Dystrophy in a Family Linked to the FCD1 LocusMEADOWS, Danielle N; BGHRARI, Allen O; AMER RIAZUDDIN, S et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 12, pp 5662-5666, issn 0146-0404, 5 p.Article