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Items: 1 to 50 of 51

1.

Latency for facultative expression of male-typical courtship behaviour by female bluehead wrasses depends on social rank: The 'priming/gating' hypothesis.

Price SM, Luong K, Bell RS, Rose GJ.

J Exp Biol. 2018 Oct 10. pii: jeb.180901. doi: 10.1242/jeb.180901. [Epub ahead of print]

PMID:
30305374
2.

A Conceptual Model for Evaluating Emergency Risk Communication in Public Health.

Seeger MW, Pechta LE, Price SM, Lubell KM, Rose DA, Sapru S, Chansky MC, Smith BJ.

Health Secur. 2018 May/Jun;16(3):193-203. doi: 10.1089/hs.2018.0020.

PMID:
29927343
3.

Using theory-based messages to motivate U.S. pregnant women to prevent cytomegalovirus infection: results from formative research.

Levis DM, Hillard CL, Price SM, Reed-Gross E, Bonilla E, Amin M, Stowell JD, Clark R, Johnson D, Mask K, Carpentieri C, Cannon MJ.

BMC Womens Health. 2017 Dec 14;17(1):131. doi: 10.1186/s12905-017-0482-z.

4.

Anacardic Acid, Salicylic Acid, and Oleic Acid Differentially Alter Cellular Bioenergetic Function in Breast Cancer Cells.

Radde BN, Alizadeh-Rad N, Price SM, Schultz DJ, Klinge CM.

J Cell Biochem. 2016 Nov;117(11):2521-32. doi: 10.1002/jcb.25544. Epub 2016 Apr 14.

PMID:
26990649
5.

Why the general dentist needs to know how to manage oral lichen planus.

Price SM, Murrah VA.

Gen Dent. 2015 Jan-Feb;63(1):16-22. Review.

PMID:
25574714
6.

Educating women about congenital cytomegalovirus: assessment of health education materials through a web-based survey.

Price SM, Bonilla E, Zador P, Levis DM, Kilgo CL, Cannon MJ.

BMC Womens Health. 2014 Nov 30;14:144. doi: 10.1186/s12905-014-0144-3.

7.

Autophagy sustains mitochondrial glutamine metabolism and growth of BrafV600E-driven lung tumors.

Strohecker AM, Guo JY, Karsli-Uzunbas G, Price SM, Chen GJ, Mathew R, McMahon M, White E.

Cancer Discov. 2013 Nov;3(11):1272-85. doi: 10.1158/2159-8290.CD-13-0397. Epub 2013 Aug 21.

8.

Canonical Wnt signaling regulates Nkx3.1 expression and luminal epithelial differentiation during prostate organogenesis.

Kruithof-de Julio M, Shibata M, Desai N, Reynon M, Halili MV, Hu YP, Price SM, Abate-Shen C, Shen MM.

Dev Dyn. 2013 Oct;242(10):1160-71. doi: 10.1002/dvdy.24008. Epub 2013 Jul 29.

9.

Molecular and clinical delineation of the 17q22 microdeletion phenotype.

Laurell T, Lundin J, Anderlid BM, Gorski JL, Grigelioniene G, Knight SJ, Krepischi AC, Nordenskjöld A, Price SM, Rosenberg C, Turnpenny PD, Vianna-Morgante AM, Nordgren A.

Eur J Hum Genet. 2013 Oct;21(10):1085-92. doi: 10.1038/ejhg.2012.306. Epub 2013 Jan 30.

10.

How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum.

Banka S, Veeramachaneni R, Reardon W, Howard E, Bunstone S, Ragge N, Parker MJ, Crow YJ, Kerr B, Kingston H, Metcalfe K, Chandler K, Magee A, Stewart F, McConnell VP, Donnelly DE, Berland S, Houge G, Morton JE, Oley C, Revencu N, Park SM, Davies SJ, Fry AE, Lynch SA, Gill H, Schweiger S, Lam WW, Tolmie J, Mohammed SN, Hobson E, Smith A, Blyth M, Bennett C, Vasudevan PC, García-Miñaúr S, Henderson A, Goodship J, Wright MJ, Fisher R, Gibbons R, Price SM, C de Silva D, Temple IK, Collins AL, Lachlan K, Elmslie F, McEntagart M, Castle B, Clayton-Smith J, Black GC, Donnai D.

Eur J Hum Genet. 2012 Apr;20(4):381-8. doi: 10.1038/ejhg.2011.220. Epub 2011 Nov 30.

11.

Regulation of extra-embryonic endoderm stem cell differentiation by Nodal and Cripto signaling.

Kruithof-de Julio M, Alvarez MJ, Galli A, Chu J, Price SM, Califano A, Shen MM.

Development. 2011 Sep;138(18):3885-95. doi: 10.1242/dev.065656.

12.

Cardiofaciocutaneous syndrome in a mother and two sons with a MEK2 mutation.

Linden HC, Price SM.

Clin Dysmorphol. 2011 Apr;20(2):86-8. doi: 10.1097/MCD.0b013e32833ff29d. No abstract available.

PMID:
21178588
13.

Epigenotype-phenotype correlations in Silver-Russell syndrome.

Wakeling EL, Amero SA, Alders M, Bliek J, Forsythe E, Kumar S, Lim DH, MacDonald F, Mackay DJ, Maher ER, Moore GE, Poole RL, Price SM, Tangeraas T, Turner CL, Van Haelst MM, Willoughby C, Temple IK, Cobben JM.

J Med Genet. 2010 Nov;47(11):760-8. doi: 10.1136/jmg.2010.079111. Epub 2010 Aug 3.

14.

Music exposure and hearing disorders: an overview.

Zhao F, Manchaiah VK, French D, Price SM.

Int J Audiol. 2010 Jan;49(1):54-64. doi: 10.3109/14992020903202520. Review.

PMID:
20001447
15.

A luminal epithelial stem cell that is a cell of origin for prostate cancer.

Wang X, Kruithof-de Julio M, Economides KD, Walker D, Yu H, Halili MV, Hu YP, Price SM, Abate-Shen C, Shen MM.

Nature. 2009 Sep 24;461(7263):495-500. doi: 10.1038/nature08361. Epub 2009 Sep 9.

16.

Inactivation of DltA modulates virulence factor expression in Streptococcus pyogenes.

Cox KH, Ruiz-Bustos E, Courtney HS, Dale JB, Pence MA, Nizet V, Aziz RK, Gerling I, Price SM, Hasty DL.

PLoS One. 2009;4(4):e5366. doi: 10.1371/journal.pone.0005366. Epub 2009 Apr 29.

17.

No effect of inversion on attentional and affective processing of facial expressions.

Lipp OV, Price SM, Tellegen CL.

Emotion. 2009 Apr;9(2):248-59. doi: 10.1037/a0014715.

PMID:
19348536
18.

Monomethylation of histone H4-lysine 20 is involved in chromosome structure and stability and is essential for mouse development.

Oda H, Okamoto I, Murphy N, Chu J, Price SM, Shen MM, Torres-Padilla ME, Heard E, Reinberg D.

Mol Cell Biol. 2009 Apr;29(8):2278-95. doi: 10.1128/MCB.01768-08. Epub 2009 Feb 17.

19.

Pain relief for the removal of femoral sheath in interventional cardiology adult patients.

Wensley CJ, Kent B, McAleer MB, Price SM, Stewart JT.

Cochrane Database Syst Rev. 2008 Oct 8;(4):CD006043. doi: 10.1002/14651858.CD006043.pub2. Review.

PMID:
18843700
20.

Mouse Fem1b interacts with the Nkx3.1 homeoprotein and is required for proper male secondary sexual development.

Wang X, Desai N, Hu YP, Price SM, Abate-Shen C, Shen MM.

Dev Dyn. 2008 Oct;237(10):2963-72. doi: 10.1002/dvdy.21694.

21.

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.

Koolen DA, Sharp AJ, Hurst JA, Firth HV, Knight SJ, Goldenberg A, Saugier-Veber P, Pfundt R, Vissers LE, Destrée A, Grisart B, Rooms L, Van der Aa N, Field M, Hackett A, Bell K, Nowaczyk MJ, Mancini GM, Poddighe PJ, Schwartz CE, Rossi E, De Gregori M, Antonacci-Fulton LL, McLellan MD 2nd, Garrett JM, Wiechert MA, Miner TL, Crosby S, Ciccone R, Willatt L, Rauch A, Zenker M, Aradhya S, Manning MA, Strom TM, Wagenstaller J, Krepischi-Santos AC, Vianna-Morgante AM, Rosenberg C, Price SM, Stewart H, Shaw-Smith C, Brunner HG, Wilkie AO, Veltman JA, Zuffardi O, Eichler EE, de Vries BB.

J Med Genet. 2008 Nov;45(11):710-20. doi: 10.1136/jmg.2008.058701. Epub 2008 Jul 15. Erratum in: J Med Genet. 2009 Aug;46(8):576.

22.

Influencing the parents of children aged 9-13 years: findings from the VERB campaign.

Price SM, Huhman M, Potter LD.

Am J Prev Med. 2008 Jun;34(6 Suppl):S267-74. doi: 10.1016/j.amepre.2008.03.004.

PMID:
18471607
23.

The VERB campaign: applying a branding strategy in public health.

Asbury LD, Wong FL, Price SM, Nolin MJ.

Am J Prev Med. 2008 Jun;34(6 Suppl):S183-7. doi: 10.1016/j.amepre.2008.03.010.

PMID:
18471598
24.

Correlates of weight-bearing physical activity among adolescent girls: results from a national survey of girls and their parents.

Price SM, McDivitt J, Weber D, Wolff LS, Massett HA, Fulton JE.

J Phys Act Health. 2008 Jan;5(1):132-45.

PMID:
18209259
25.

Characterization of a recurrent 15q24 microdeletion syndrome.

Sharp AJ, Selzer RR, Veltman JA, Gimelli S, Gimelli G, Striano P, Coppola A, Regan R, Price SM, Knoers NV, Eis PS, Brunner HG, Hennekam RC, Knight SJ, de Vries BB, Zuffardi O, Eichler EE.

Hum Mol Genet. 2007 Mar 1;16(5):567-72. Epub 2007 Mar 14.

PMID:
17360722
26.

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.

Sharp AJ, Hansen S, Selzer RR, Cheng Z, Regan R, Hurst JA, Stewart H, Price SM, Blair E, Hennekam RC, Fitzpatrick CA, Segraves R, Richmond TA, Guiver C, Albertson DG, Pinkel D, Eis PS, Schwartz S, Knight SJ, Eichler EE.

Nat Genet. 2006 Sep;38(9):1038-42. Epub 2006 Aug 13.

PMID:
16906162
27.

Non-cell-autonomous role for Cripto in axial midline formation during vertebrate embryogenesis.

Chu J, Ding J, Jeays-Ward K, Price SM, Placzek M, Shen MM.

Development. 2005 Dec;132(24):5539-51. Epub 2005 Nov 16.

28.

Foxn4 controls the genesis of amacrine and horizontal cells by retinal progenitors.

Li S, Mo Z, Yang X, Price SM, Shen MM, Xiang M.

Neuron. 2004 Sep 16;43(6):795-807.

29.

Genetic evidence for nonredundant functional cooperativity between NPC1 and NPC2 in lipid transport.

Sleat DE, Wiseman JA, El-Banna M, Price SM, Verot L, Shen MM, Tint GS, Vanier MT, Walkley SU, Lobel P.

Proc Natl Acad Sci U S A. 2004 Apr 20;101(16):5886-91. Epub 2004 Apr 7.

30.
31.

Inhibition of excess nodal signaling during mouse gastrulation by the transcriptional corepressor DRAP1.

Iratni R, Yan YT, Chen C, Ding J, Zhang Y, Price SM, Reinberg D, Shen MM.

Science. 2002 Dec 6;298(5600):1996-9.

32.

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

Monk D, Bentley L, Hitchins M, Myler RA, Clayton-Smith J, Ismail S, Price SM, Preece MA, Stanier P, Moore GE.

Hum Genet. 2002 Oct;111(4-5):376-87. Epub 2002 Aug 16.

PMID:
12384779
33.

Hearing loss caused by progressive degeneration of cochlear hair cells in mice deficient for the Barhl1 homeobox gene.

Li S, Price SM, Cahill H, Ryugo DK, Shen MM, Xiang M.

Development. 2002 Jul;129(14):3523-32.

34.

Msx homeobox genes inhibit differentiation through upregulation of cyclin D1.

Hu G, Lee H, Price SM, Shen MM, Abate-Shen C.

Development. 2001 Jun;128(12):2373-84.

35.

The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria.

Price SM, Stanhope R, Garrett C, Preece MA, Trembath RC.

J Med Genet. 1999 Nov;36(11):837-42.

36.

Conserved requirement for EGF-CFC genes in vertebrate left-right axis formation.

Yan YT, Gritsman K, Ding J, Burdine RD, Corrales JD, Price SM, Talbot WS, Schier AF, Shen MM.

Genes Dev. 1999 Oct 1;13(19):2527-37.

37.

Genetics of Silver-Russell syndrome.

Wakeling EL, Abu-Amero S, Price SM, Stanier P, Trembath RC, Moore GE, Preece MA.

Horm Res. 1998;49 Suppl 2:32-6. Review.

PMID:
9730670
38.

Genetics of silver-russell syndrome

Wakeling EL, Abu-Amero S, Price SM, Stanier P, Trembath RC, Moore GE, Preece MA.

Horm Res. 1998;49(# Suppl 2):32-6. No abstract available.

PMID:
9716825
39.

Four cases of amelia of the upper limb associated with anal atresia--is this VACTERL with extreme limb involvement?

Price SM, Berry AC, Raymond FL, Turnpenny P, Young ID.

Clin Dysmorphol. 1998 Jan;7(1):35-40. Review.

PMID:
9546828
40.

Maternal uniparental disomy 7 in Silver-Russell syndrome.

Preece MA, Price SM, Davies V, Clough L, Stanier P, Trembath RC, Moore GE.

J Med Genet. 1997 Jan;34(1):6-9.

41.

Familial exudative vitreoretinopathy linked to D11S533 in a large Asian family with consanguinity.

Price SM, Periam N, Humphries A, Woodruff G, Trembath RC.

Ophthalmic Genet. 1996 Jun;17(2):53-7.

PMID:
8832721
42.

The attitudes of midwives to maternal serum screening for Down's syndrome.

Khalid L, Price SM, Barrow M.

Public Health. 1994 Mar;108(2):131-6.

PMID:
8183968
43.

Circulating high molecular weight IgG fibronectin complexes in myeloproliferative disorders.

Baglin TP, Price SM, Boughton BJ.

J Clin Pathol. 1990 Feb;43(2):102-5.

44.

A reversible defect of platelet PDGF content in myeloproliferative disorders.

Baglin TP, Price SM, Boughton BJ.

Br J Haematol. 1988 Aug;69(4):483-6.

PMID:
3408684
45.

Composition of immune complexes and their relation to plasma fibronectin in chronic myeloproliferative disorders.

Baglin TP, Simpson AW, Price SM, Boughton BJ.

J Clin Pathol. 1987 Dec;40(12):1468-71.

46.
47.

Gastrict carcinoma with pseudohyperparathyroidism in a horse.

Meuten DJ, Price SM, Seiler RM, Krook L.

Cornell Vet. 1978 Apr;68(2):179-95.

48.
49.

New world leishmaniasis. Serologic aids to diagnosis.

Price SM, Silvers DN.

Arch Dermatol. 1977 Oct;113(10):1415-6.

PMID:
334085
50.

Barbers' interdigital hair sinus.

Price SM, Popkin GL.

Arch Dermatol. 1976 Apr;112(4):523-4.

PMID:
131514

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