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Definition, causes, and consequences of Hamm (idiom of distress in Arabic) in the Palestinian context: a qualitative study.

Nasir AA, Salah R, Ahmad AS, Hijleh SA, Kattab SA, Kurd AA, Sharif RA, Amro R, Khatib A, Mousa H, Shamasnah W, Shqerat K, Giacaman R.

Lancet. 2018 Feb 21;391 Suppl 2:S1. doi: 10.1016/S0140-6736(18)30367-2. Epub 2018 Feb 21.


Novel synergistic hydrous iron-nickel-manganese (HINM) trimetal oxide for hazardous arsenite removal.

Nasir AM, Goh PS, Ismail AF.

Chemosphere. 2018 Jun;200:504-512. doi: 10.1016/j.chemosphere.2018.02.126. Epub 2018 Feb 23.


Identification of novel L2HGDH mutation in a large consanguineous Pakistani family- a case report.

Ullah MI, Nasir A, Ahmad A, Harlalka GV, Ahmad W, Hassan MJ, Baple EL, Crosby AH, Chioza BA.

BMC Med Genet. 2018 Feb 20;19(1):25. doi: 10.1186/s12881-018-0532-x.


A novel homozygous missense variant in NECTIN4 (PVRL4) causing ectodermal dysplasia cutaneous syndactyly syndrome.

Ahmad F, Nasir A, Thiele H, Umair M, Borck G, Ahmad W.

Ann Hum Genet. 2018 Feb 12. doi: 10.1111/ahg.12244. [Epub ahead of print]


The Many Faces of Intestinal Tract Gastric Heterotopia; A Series of Four Cases Highlighting Clinical and Pathological Heterogeneity.

Nasir A, Amateau SK, Khan S, Simpson RW, Snover DC, Amin K.

Hum Pathol. 2018 Jan 7. pii: S0046-8177(18)30004-2. doi: 10.1016/j.humpath.2018.01.003. [Epub ahead of print]


A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family.

Khan AK, Muhammad N, Khan SA, Ullah W, Nasir A, Afzal S, Ramzan K, Basit S, Khan S.

Ann Hum Genet. 2017 Dec 28. doi: 10.1111/ahg.12239. [Epub ahead of print]


Engineering an aldehyde dehydrogenase toward its substrates, 3-hydroxypropanal and NAD+, for enhancing the production of 3-hydroxypropionic acid.

Park YS, Choi UJ, Nam NH, Choi SJ, Nasir A, Lee SG, Kim KJ, Jung GY, Choi S, Shim JY, Park S, Yoo TH.

Sci Rep. 2017 Dec 7;7(1):17155. doi: 10.1038/s41598-017-15400-x.


Novel duplication mutation of the DYSF gene in a Pakistani family with Miyoshi Myopathy.

Ullah MI, Ahmad A, Zarkovic M, Shah SS, Nasir A, Mahmood S, Ahmad W, Hubner CA, Hassan MJ.

Saudi Med J. 2017 Dec;38(12):1190-1195. doi: 10.15537/smj.2017.12.20989.


Clinical outcomes after open locked intramedullary nailing of closed femoral shaft fractures for adult patients in a Nigerian Hospital.

Salawu ON, Ibraheem GH, Babalola OM, Kadir DM, Ahmed BA, Agaja SB, Olawepo A, Nasir AA.

Niger J Clin Pract. 2017 Oct;20(10):1316-1321. doi: 10.4103/njcp.njcp_294_16.


Do Viruses Exchange Genes across Superkingdoms of Life?

Malik SS, Azem-E-Zahra S, Kim KM, Caetano-Anollés G, Nasir A.

Front Microbiol. 2017 Oct 31;8:2110. doi: 10.3389/fmicb.2017.02110. eCollection 2017.


Retention of Interstitial Genes between TMPRSS2 and ERG Is Associated with Low-Risk Prostate Cancer.

Murphy SJ, Kosari F, Karnes RJ, Nasir A, Johnson SH, Gaitatzes AG, Smadbeck JB, Rangel LJ, Vasmatzis G, Cheville JC.

Cancer Res. 2017 Nov 15;77(22):6157-6167. doi: 10.1158/0008-5472.CAN-17-0529. Epub 2017 Nov 10.


A phase 2a randomized controlled study to evaluate the pharmacokinetic, safety, tolerability and clinical effect of topically applied Umeclidinium in subjects with primary axillary hyperhidrosis.

Nasir A, Bissonnette R, Maari C, DuBois J, Pene Dumitrescu T, Haddad J, Yamaguchi Y, Dalessandro M.

J Eur Acad Dermatol Venereol. 2018 Jan;32(1):145-151. doi: 10.1111/jdv.14651. Epub 2017 Nov 7.


NUMBL Interacts with TAK1, TRAF6 and NEMO to Negatively Regulate NF-κB Signaling During Osteoclastogenesis.

Swarnkar G, Chen TH, Arra M, Nasir AM, Mbalaviele G, Abu-Amer Y.

Sci Rep. 2017 Oct 3;7(1):12600. doi: 10.1038/s41598-017-12707-7.


The great impostor: Lues maligna in an HIV-infected male.

Mena Lora AJ, Braniecki M, Nasir A, Brito M.

SAGE Open Med Case Rep. 2017 Sep 19;5:2050313X17731050. doi: 10.1177/2050313X17731050. eCollection 2017.


The Interplay of Genetics and Environmental Factors in the Development of Obesity.

Sheikh AB, Nasrullah A, Haq S, Akhtar A, Ghazanfar H, Nasir A, Afzal RM, Bukhari MM, Chaudhary AY, Naqvi SW.

Cureus. 2017 Jul 6;9(7):e1435. doi: 10.7759/cureus.1435. Review.


A Preliminary List of Horizontally Transferred Genes in Prokaryotes Determined by Tree Reconstruction and Reconciliation.

Jeong H, Nasir A.

Front Genet. 2017 Aug 28;8:112. doi: 10.3389/fgene.2017.00112. eCollection 2017.


Disparities in patient record completeness with respect to the health care utilization project.

Nasir A, Liu X, Gurupur V, Qureshi Z.

Health Informatics J. 2017 Jul 1:1460458217716005. doi: 10.1177/1460458217716005. [Epub ahead of print]


A Unique Case of Empyema Secondary to Amoebic Liver Abscess.

Nasrullah A, Haq S, Ghazanfar H, Sheikh AB, Akhtar A, Zafar R, Nasir A, Shaukat F, Abbas AH.

Cureus. 2017 Jun 21;9(6):e1377. doi: 10.7759/cureus.1377.


Phylogenetic Tracings of Proteome Size Support the Gradual Accretion of Protein Structural Domains and the Early Origin of Viruses from Primordial Cells.

Nasir A, Kim KM, Caetano-Anollés G.

Front Microbiol. 2017 Jun 23;8:1178. doi: 10.3389/fmicb.2017.01178. eCollection 2017.


Cross-Platform Comparison of Computer-assisted Image Analysis Quantification of In Situ mRNA Hybridization in Investigative Pathology.

Holzer TR, Hanson JC, Wray EM, Bailey JA, Kennedy KR, Finnegan PR, Nasir A, Credille KM.

Appl Immunohistochem Mol Morphol. 2017 Jul 4. doi: 10.1097/PAI.0000000000000542. [Epub ahead of print]


Hybrid spiral-dynamic bacteria-chemotaxis algorithm with application to control two-wheeled machines.

Goher KM, Almeshal AM, Agouri SA, Nasir ANK, Tokhi MO, Alenezi MR, Al Zanki T, Fadlallah SO.

Robotics Biomim. 2017;4(1):3. doi: 10.1186/s40638-017-0059-1. Epub 2017 Jun 16.


Genomic rearrangements in sporadic lymphangioleiomyomatosis: an evolving genetic story.

Murphy SJ, Terra SB, Harris FR, Nasir A, Voss JS, Smadbeck JB, Johnson SH, Serla V, Ryu JH, Yi ES, Kipp BR, Vasmatzis G, Carmona EM.

Mod Pathol. 2017 Sep;30(9):1223-1233. doi: 10.1038/modpathol.2017.52. Epub 2017 Jun 23.


Long-term evolution of viruses: A Janus-faced balance.

Nasir A, Kim KM, Caetano-Anollés G.

Bioessays. 2017 Aug;39(8). doi: 10.1002/bies.201700026. Epub 2017 Jun 16. Review.


Lokiarchaea are close relatives of Euryarchaeota, not bridging the gap between prokaryotes and eukaryotes.

Da Cunha V, Gaia M, Gadelle D, Nasir A, Forterre P.

PLoS Genet. 2017 Jun 12;13(6):e1006810. doi: 10.1371/journal.pgen.1006810. eCollection 2017 Jun.


Modeling Congenital Hyperinsulinism with ABCC8-Deficient Human Embryonic Stem Cells Generated by CRISPR/Cas9.

Guo D, Liu H, Ruzi A, Gao G, Nasir A, Liu Y, Yang F, Wu F, Xu G, Li YX.

Sci Rep. 2017 Jun 9;7(1):3156. doi: 10.1038/s41598-017-03349-w.


A homozygous potentially pathogenic variant in the PAXBP1 gene in a large family with global developmental delay and myopathic hypotonia.

Alharby E, Albalawi AM, Nasir A, Alhijji SA, Mahmood A, Ramzan K, Abdusamad F, Aljohani A, Abdelsalam O, Eldardear A, Basit S.

Clin Genet. 2017 Dec;92(6):579-586. doi: 10.1111/cge.13051. Epub 2017 Sep 15.


Differential expression of VEGFR2 protein in HER2 positive primary human breast cancer: potential relevance to anti-angiogenic therapies.

Nasir A, Holzer TR, Chen M, Man MZ, Schade AE.

Cancer Cell Int. 2017 May 19;17:56. doi: 10.1186/s12935-017-0427-5. eCollection 2017.


Complete genome of a metabolically-diverse marine bacterium Shewanella japonica KCTC 22435T.

Kim KM, Choe H, Kim BK, Nasir A.

Mar Genomics. 2017 Oct;35:39-42. doi: 10.1016/j.margen.2017.05.004. Epub 2017 May 15.


Psychometric properties of Conversion Disorder Scale- Revised (CDS) for children.

Ijaz T, Nasir A, Sarfraz N, Ijaz S.

J Pak Med Assoc. 2017 May;67(5):725-730.


EGFR mediates activation of RET in lung adenocarcinoma with neuroendocrine differentiation characterized by ASCL1 expression.

Bhinge K, Yang L, Terra S, Nasir A, Muppa P, Aubry MC, Yi J, Janaki N, Kovtun IV, Murphy SJ, Halling G, Rahi H, Mansfield A, de Andrade M, Yang P, Vasmatzis G, Peikert T, Kosari F.

Oncotarget. 2017 Apr 18;8(16):27155-27165. doi: 10.18632/oncotarget.15676.


Accessory Spleen in the Greater Omentum: Embryology and Revisited Prevalence Rates.

Gill N, Nasir A, Douglin J, Pretterklieber B, Steinke H, Pretterklieber M, Cotofana S.

Cells Tissues Organs. 2017;203(6):374-378. doi: 10.1159/000458754. Epub 2017 Apr 19.


A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family.

Khan AK, Muhammad N, Aziz A, Khan SA, Shah K, Nasir A, Khan MA, Khan S.

BMC Med Genet. 2017 Apr 12;18(1):42. doi: 10.1186/s12881-017-0402-y.


Isolation of Saccharomyces Cerevisiae from Pineapple and Orange and Study of Metal's Effectiveness on Ethanol Production.

Nasir A, Rahman SS, Hossain MM, Choudhury N.

Eur J Microbiol Immunol (Bp). 2017 Feb 27;7(1):76-91. doi: 10.1556/1886.2016.00035. eCollection 2017 Mar.


Identification of Capsid/Coat Related Protein Folds and Their Utility for Virus Classification.

Nasir A, Caetano-Anollés G.

Front Microbiol. 2017 Mar 10;8:380. doi: 10.3389/fmicb.2017.00380. eCollection 2017.


Corrigendum to "Clinical and genetic studies in patients with Lafora disease from Pakistan"[J. Neurol. Sci. 373 (2017) 263-267].

Ahmad A, Dad R, Ullah MI, Baig TA, Ahmad IN, Nasir A, Hübner CA, Hassan MJ.

J Neurol Sci. 2017 Apr 15;375:281. doi: 10.1016/j.jns.2017.02.010. Epub 2017 Feb 12. No abstract available.


Phase 1 study of narnatumab, an anti-RON receptor monoclonal antibody, in patients with advanced solid tumors.

LoRusso PM, Gounder M, Jalal SI, André V, Kambhampati SRP, Loizos N, Hall J, Holzer TR, Nasir A, Cosaert J, Kauh J, Chiorean EG.

Invest New Drugs. 2017 Aug;35(4):442-450. doi: 10.1007/s10637-016-0413-0. Epub 2017 Feb 4.


Clinical and genetic studies in patients with Lafora disease from Pakistan.

Ahmad A, Dad R, Ullah MI, Baig TA, Ahmad IN, Nasir A, Hübner CA, Hassan MJ.

J Neurol Sci. 2017 Feb 15;373:263-267. doi: 10.1016/j.jns.2017.01.010. Epub 2017 Jan 4.


Arguments Reinforcing the Three-Domain View of Diversified Cellular Life.

Nasir A, Kim KM, Da Cunha V, Caetano-Anollés G.

Archaea. 2016 Dec 5;2016:1851865. doi: 10.1155/2016/1851865. eCollection 2016. Review.


Erratum to: Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant.

Moiz B, Nasir A, Khan SA, Kherani SA, Qadir M.

BMC Pediatr. 2016 Dec 9;16(1):209. No abstract available.


Complete Genome Sequence of Nitrilotriacetate-Degrading Aminobacter aminovorans KCTC 2477T.

Lee SH, Choe H, Nasir A, Park DS, Kim KM.

Genome Announc. 2016 Dec 8;4(6). pii: e01363-16. doi: 10.1128/genomeA.01363-16.


Synchronous Microscopic Epstein-Barr Virus-Positive Diffuse Large B-Cell Lymphoma of the Adrenal and Lymphoplasmacytic Lymphoma: De Novo Disease or Transformation?

Moonim MT, Nasir A, Hubbard J, Ketley N, Fields P.

Int J Surg Pathol. 2017 Jun;25(4):326-332. doi: 10.1177/1066896916681843. Epub 2016 Dec 4.


Intraoperative diagnosis of mitral valve endocarditis secondary to Paenibacillus provencensis.

Pinho-Gomes AC, Nasir A, Mosca R, Mirza S, Kadir I.

Ann R Coll Surg Engl. 2017 Feb;99(2):e54-e55. doi: 10.1308/rcsann.2016.0312. Epub 2016 Oct 28.


Serological, molecular detection and potential risk factors associated with camel brucellosis in Pakistan.

Fatima S, Khan I, Nasir A, Younus M, Saqib M, Melzer F, Neubauer H, El-Adawy H.

Trop Anim Health Prod. 2016 Dec;48(8):1711-1718. Epub 2016 Sep 27.


Two-hourly versus 3-hourly feeding for very low birthweight infants: a randomised controlled trial.

Ibrahim NR, Kheng TH, Nasir A, Ramli N, Foo JLK, Syed Alwi SH, Van Rostenberghe H.

Arch Dis Child Fetal Neonatal Ed. 2017 May;102(3):F225-F229. doi: 10.1136/archdischild-2015-310246. Epub 2016 Sep 26.


Novel homozygous sequence variants in the GDF5 gene underlie acromesomelic dysplasia type-grebe in consanguineous families.

Umair M, Rafique A, Ullah A, Ahmad F, Ali RH, Nasir A, Ansar M, Ahmad W.

Congenit Anom (Kyoto). 2017 Mar;57(2):45-51. doi: 10.1111/cga.12187.


Markedly Increased Rate of Primary Liver Malignancies at Autopsy in Male US Veterans.

Nasir A, Manivel JC, Yousaf H, Albrecht JH, Dykoski R, Mesa H.

Clin Gastroenterol Hepatol. 2017 Feb;15(2):316-318. doi: 10.1016/j.cgh.2016.08.025. Epub 2016 Aug 26. No abstract available.


Hypomorphic MKS1 mutation in a Pakistani family with mild Joubert syndrome and atypical features: Expanding the phenotypic spectrum of MKS1-related ciliopathies.

Irfanullah, Khan S, Ullah I, Nasir A, Meijer CA, Laurense-Bik M, den Dunnen JT, Ruivenkamp CA, Hoffer MJ, Santen GW, Ahmad W.

Am J Med Genet A. 2016 Dec;170(12):3289-3293. doi: 10.1002/ajmg.a.37934. Epub 2016 Aug 29.


Dissemination and spread of New Delhi Metallo-beta-lactamase-1 Superbugs in hospital settings.

Khan E, Irfan S, Sultan BA, Nasir A, Hasan R.

J Pak Med Assoc. 2016 Aug;66(8):999-1004.


A New Paradigm to Analyze Data Completeness of Patient Data.

Nasir A, Gurupur V, Liu X.

Appl Clin Inform. 2016 Aug 3;7(3):745-64. doi: 10.4338/ACI-2016-04-RA-0063.


A novel homozygous mutation disrupting the initiation codon in the SLURP1 gene underlies mal de Meleda in a consanguineous family.

Shah K, Nasir A, Irfanullah, Shahzad S, Khan S, Ahmad W.

Clin Exp Dermatol. 2016 Aug;41(6):675-679. doi: 10.1111/ced.12864. Epub 2016 Jul 5.


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