13 results for author:"Siddique N." in Literature citations
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| Sequence and phylogenetic analysis of highly pathogenic avian influenza H5N1 viruses isolated during 2006-2008 outbreaks in Pakistan reveals genetic diversity. Siddique N., Naeem K., Abbas M.A., Ahmed Z., Malik S.A. Virol. J. 9:300-300(2012) · UniProtKB (32) |
| Isolation, identification, and phylogenetic analysis of reassortant low-pathogenic avian influenza virus H3N1 from Pakistan. Siddique N., Naeem K., Ahmed Z., Abbas M.A., Farooq S., Malik S.A. Poult. Sci. 91:129-138(2012) · UniProtKB (11) |
| SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis. Fecto F., Yan J., Vemula S.P., Liu E., Yang Y., Chen W., Zheng J.G., Shi Y., Siddique N., Arrat H. et al. Arch. Neurol. 68:1440-1446(2011) · Mapped (3) |
| Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Deng H.X., Chen W., Hong S.T., Boycott K.M., Gorrie G.H., Siddique N., Yang Y., Fecto F., Shi Y., Zhai H. et al. |
| Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations. Deng H.X., Bigio E.H., Zhai H., Fecto F., Ajroud K., Shi Y., Yan J., Mishra M., Ajroud-Driss S., Heller S. et al. Arch. Neurol. 68:1057-1061(2011) · Mapped (9) |
| Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4. Deng H.X., Klein C.J., Yan J., Shi Y., Wu Y., Fecto F., Yau H.J., Yang Y., Zhai H., Siddique N. et al. Nat. Genet. 42:165-169(2010) · UniProtKB (1) |
| Age and founder effect of SOD1 A4V mutation causing ALS. Saeed M., Yang Y., Deng H.X., Hung W.Y., Siddique N., Dellefave L., Gellera C., Andersen P.M., Siddique T. Neurology 72:1634-1639(2009) · Mapped (2) |
| Riluzole metabolism and CYP1A1/2 polymorphisms in patients with ALS. Ajroud-Driss S., Saeed M., Khan H., Siddique N., Hung W.Y., Sufit R., Heller S., Armstrong J., Casey P., Siddique T. et al. Amyotroph Lateral Scler 8:305-309(2007) · Mapped (12) |
| Lack of association of VEGF promoter polymorphisms with sporadic ALS. Chen W., Saeed M., Mao H., Siddique N., Dellefave L., Hung W.Y., Deng H.X., Sufit R.L., Heller S.L., Haines J.L. et al. Neurology 67:508-510(2006) · Mapped (7) |
| Paraoxonase cluster polymorphisms are associated with sporadic ALS. Saeed M., Siddique N., Hung W.Y., Usacheva E., Liu E., Sufit R.L., Heller S.L., Haines J.L., Pericak-Vance M., Siddique T. Neurology 67:771-776(2006) · Mapped (12) |
| Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis. Li Y.J., Pericak-Vance M.A., Haines J.L., Siddique N., McKenna-Yasek D., Hung W.Y., Sapp P., Allen C.I., Chen W., Hosler B. et al. Neurogenetics 5:209-213(2004) · Mapped (5) |
| A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset, incomplete penetrance and a sensory neuropathy. Rezania K., Yan J., Dellefave L., Deng H.X., Siddique N., Pascuzzi R.T., Siddique T., Roos R.P. Amyotroph. Lateral Scler. Other Motor Neuron Disord. 4:162-166(2003) · Mapped (2) |
| Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis. Siddique T., Pericak-Vance M.A., Caliendo J., Hong S.T., Hung W.Y., Kaplan J., McKenna-Yasek D., Rimmler J.B., Sapp P., Saunders A.M. et al. Neurogenetics 1:213-216(1998) · Mapped (5) |