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Items: 28


Phenotypic dissection of the mouse Ren1d knockout by complementation with human renin.

Buckley C, Nelson RJ, Mullins LJ, Sharp MGF, Fleming S, Kenyon CJ, Semprini S, Steppan D, Peti-Peterdi J, Kurtz A, Christian H, Mullins JJ.

J Biol Chem. 2018 Jan 26;293(4):1151-1162. doi: 10.1074/jbc.RA117.000160. Epub 2017 Nov 9.


HIV-1 early and late diagnosis in the Emilia Romagna Region (Italy): a three year study.

Musumeci G, Magnani G, Bon I, Longo S, Bertoldi A, Degli Antoni AM, Rossi MR, Ruggeri A, Sambri V, Semprini S, Sighinolfi L, Ursitti MA, Zerbini A, Colangeli V, Calza L, Finarelli AC, Massimiliani E, Re MC.

New Microbiol. 2016 Oct;39(4):241-246. Epub 2016 Sep 13.


Three-year retrospective analysis of the incidence of Toxoplasma gondii infection in pregnant women living in the Greater Romagna Area (northeastern Italy).

Billi P, Della Strada M, Pierro A, Semprini S, Tommasini N, Sambri V.

Clin Microbiol Infect. 2016 Jun;22(6):572.e1-3. doi: 10.1016/j.cmi.2016.02.010. Epub 2016 Mar 9.


Role of Estrogen Response Element in the Human Prolactin Gene: Transcriptional Response and Timing.

McNamara AV, Adamson AD, Dunham LS, Semprini S, Spiller DG, McNeilly AS, Mullins JJ, Davis JR, White MR.

Mol Endocrinol. 2016 Feb;30(2):189-200. doi: 10.1210/me.2015-1186. Epub 2015 Dec 21.


Reply to "Better method for evaluating a new laboratory test for syphilis".

Enders M, Gleich M, Mühlbacher A, Sakuldamrongpanich T, Turhan A, Sertöz R, Semprini S, Sambri V.

Clin Vaccine Immunol. 2015 May;22(5):607-8. doi: 10.1128/CVI.00109-15. No abstract available.


Performance evaluation of the Elecsys syphilis assay for the detection of total antibodies to Treponema pallidum.

Enders M, Hunjet A, Gleich M, Imdahl R, Mühlbacher A, Schennach H, Chaiwong K, Sakuldamrongpanich T, Turhan A, Sertöz R, Wolf E, Mayer W, Tao C, Wang LL, Semprini S, Sambri V.

Clin Vaccine Immunol. 2015 Jan;22(1):17-26. doi: 10.1128/CVI.00505-14. Epub 2014 Oct 29.


Use of fiber optic technology to measure the effects of anesthesia on luciferase reaction kinetics.

Semprini S, Saunter CD, Ludwig M, Girkin JM, Mullins JJ.

J Am Assoc Lab Anim Sci. 2012 Nov;51(6):820-4.


Micro-endoscope for in vivo widefield high spatial resolution fluorescent imaging.

Saunter CD, Semprini S, Buckley C, Mullins J, Girkin JM.

Biomed Opt Express. 2012 Jun 1;3(6):1274-8. doi: 10.1364/BOE.3.001274. Epub 2012 May 4.


Peritonitis activates transcription of the human prolactin locus in myeloid cells in a humanized transgenic rat model.

Semprini S, McNamara AV, Awais R, Featherstone K, Harper CV, McNeilly JR, Patist A, Rossi AG, Dransfield I, McNeilly AS, Davis JR, White MR, Mullins JJ.

Endocrinology. 2012 Jun;153(6):2724-34. doi: 10.1210/en.2011-1926. Epub 2012 Apr 11.


Pulsatile patterns of pituitary hormone gene expression change during development.

Featherstone K, Harper CV, McNamara A, Semprini S, Spiller DG, McNeilly J, McNeilly AS, Mullins JJ, White MR, Davis JR.

J Cell Sci. 2011 Oct 15;124(Pt 20):3484-91. doi: 10.1242/jcs.088500. Epub 2011 Oct 7.


Dynamic analysis of stochastic transcription cycles.

Harper CV, Finkenstädt B, Woodcock DJ, Friedrichsen S, Semprini S, Ashall L, Spiller DG, Mullins JJ, Rand DA, Davis JR, White MR.

PLoS Biol. 2011 Apr;9(4):e1000607. doi: 10.1371/journal.pbio.1000607. Epub 2011 Apr 12.


Dynamic organisation of prolactin gene expression in living pituitary tissue.

Harper CV, Featherstone K, Semprini S, Friedrichsen S, McNeilly J, Paszek P, Spiller DG, McNeilly AS, Mullins JJ, Davis JR, White MR.

J Cell Sci. 2010 Feb 1;123(Pt 3):424-30. doi: 10.1242/jcs.060434.


Real-time visualization of human prolactin alternate promoter usage in vivo using a double-transgenic rat model.

Semprini S, Friedrichsen S, Harper CV, McNeilly JR, Adamson AD, Spiller DG, Kotelevtseva N, Brooker G, Brownstein DG, McNeilly AS, White MR, Davis JR, Mullins JJ.

Mol Endocrinol. 2009 Apr;23(4):529-38. doi: 10.1210/me.2008-0399. Epub 2009 Jan 15.


Human prolactin gene promoter regulation by estrogen: convergence with tumor necrosis factor-alpha signaling.

Adamson AD, Friedrichsen S, Semprini S, Harper CV, Mullins JJ, White MR, Davis JR.

Endocrinology. 2008 Feb;149(2):687-94. Epub 2007 Nov 15.


Cryptic loxP sites in mammalian genomes: genome-wide distribution and relevance for the efficiency of BAC/PAC recombineering techniques.

Semprini S, Troup TJ, Kotelevtseva N, King K, Davis JR, Mullins LJ, Chapman KE, Dunbar DR, Mullins JJ.

Nucleic Acids Res. 2007;35(5):1402-10. Epub 2007 Feb 6.


Tumor necrosis factor-alpha activates the human prolactin gene promoter via nuclear factor-kappaB signaling.

Friedrichsen S, Harper CV, Semprini S, Wilding M, Adamson AD, Spiller DG, Nelson G, Mullins JJ, White MR, Davis JR.

Endocrinology. 2006 Feb;147(2):773-81. Epub 2005 Oct 27.


Construction and purification of pSABR 01, a pUC19-derived vector optimized for cloning full-length cDNA.

Semprini S, Collins CC, Goncz KC, Novelli G, Gruenert DC.

Biotechnol Lett. 2003 Aug;25(15):1275-80.


Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11.

Salehi LB, Mangino M, De Serio S, De Cicco D, Capon F, Semprini S, Pizzuti A, Novelli G, Dallapiccola B.

Hum Genet. 2002 Oct;111(4-5):401-4. Epub 2002 Aug 21.


Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees.

Semprini S, Capon F, Tacconelli A, Giardina E, Orecchia A, Mingarelli R, Gobello T, Zambruno G, Botta A, Fabrizi G, Novelli G.

Hum Genet. 2002 Oct;111(4-5):310-3. Epub 2002 Aug 21.


Fine mapping of the PSORS4 psoriasis susceptibility region on chromosome 1q21.

Capon F, Semprini S, Chimenti S, Fabrizi G, Zambruno G, Murgia S, Carcassi C, Fazio M, Mingarelli R, Dallapiccola B, Novelli G.

J Invest Dermatol. 2001 May;116(5):728-30.


A single strand conformation polymorphism-based carrier test for spinal muscular atrophy.

Semprini S, Tacconelli A, Capon F, Brancati F, Dallapiccola B, Novelli G.

Genet Test. 2001 Spring;5(1):33-7.


Absence of correlation between BMP-4 polymorphism and postmenopausal osteoporosis in Italian women.

Semprini S, Mango R, Brancati F, Dallapiccola B, Becherini L, Novelli G, De Lorenzo A, Brandi ML, Gennari L.

Calcif Tissue Int. 2000 Jul;67(1):93-4.


Evidence for interaction between psoriasis-susceptibility loci on chromosomes 6p21 and 1q21.

Capon F, Semprini S, Dallapiccola B, Novelli G.

Am J Hum Genet. 1999 Dec;65(6):1798-800. No abstract available.


A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13.

Servidei S, Capon F, Spinazzola A, Mirabella M, Semprini S, de Rosa G, Gennarelli M, Sangiuolo F, Ricci E, Mohrenweiser HW, Dallapiccola B, Tonali P, Novelli G.

Neurology. 1999 Sep 11;53(4):830-7.


Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibility.

Semprini S, Capon F, Bovolenta S, Bruscia E, Pizzuti A, Fabrizi G, Schietroma C, Zambruno G, Dallapiccola B, Novelli G.

Hum Genet. 1999 Feb;104(2):130-4.


Searching for psoriasis susceptibility genes in Italy: genome scan and evidence for a new locus on chromosome 1.

Capon F, Novelli G, Semprini S, Clementi M, Nudo M, Vultaggio P, Mazzanti C, Gobello T, Botta A, Fabrizi G, Dallapiccola B.

J Invest Dermatol. 1999 Jan;112(1):32-5.


A possible role of NAIP gene deletions in sex-related spinal muscular atrophy phenotype variation.

Novelli G, Semprini S, Capon F, Dallapiccola B.

Neurogenetics. 1997 May;1(1):29-30.


Deletion analysis of SMN and NAIP genes in spinal muscular atrophy Italian families.

Capon F, Levato C, Semprini S, Pizzuti A, Merlini L, Novelli G, Dallapiccola B.

Muscle Nerve. 1996 Mar;19(3):378-80. No abstract available.


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