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Items: 1 to 20 of 153

1.

Congenital Capillary Proliferation of the Kidney: A Distinctive Renal Vascular Lesion of Childhood.

Cajaiba MM, North PE, Gong S, Dickman PS, Mroczek-Musulman E, Sauer DA, Perlman EJ.

Hum Pathol. 2017 May 26. pii: S0046-8177(17)30176-4. doi: 10.1016/j.humpath.2017.05.018. [Epub ahead of print]

PMID:
28554576
2.

Mimickers of Infantile Hemangiomas.

Brockman RM, Humphrey SR, Moe DC, North PE, King DM, Jensen JN, Siegel DH, Drolet BA.

Pediatr Dermatol. 2017 May;34(3):331-336. doi: 10.1111/pde.13127.

PMID:
28523875
3.

Successful Application of Whole Genome Sequencing in a Medical Genetics Clinic.

Bick D, Fraser PC, Gutzeit MF, Harris JM, Hambuch TM, Helbling DC, Jacob HJ, Kersten JN, Leuthner SR, May T, North PE, Prisco SZ, Schuler BA, Shimoyama M, Strong KA, Van Why SK, Veith R, Verbsky J, Weborg AM Jr, Wilk BM, Willoughby RE Jr, Worthey EA, Dimmock DP.

J Pediatr Genet. 2017 Jun;6(2):61-76. doi: 10.1055/s-0036-1593968. Epub 2016 Nov 28.

PMID:
28496993
4.

Protocol for a multicentre study to assess feasibility, acceptability, effectiveness and direct costs of TRIumPH (Treatment and Recovery In PsycHosis): integrated care pathway for psychosis.

Rathod S, Garner C, Griffiths A, Dimitrov BD, Newman-Taylor K, Woodfine C, Hansen L, Tabraham P, Ward K, Asher C, Phiri P, Naeem F, North P, Munshi T, Kingdon D.

BMJ Open. 2016 Dec 21;6(12):e012751. doi: 10.1136/bmjopen-2016-012751.

5.

Leveraging a Sturge-Weber Gene Discovery: An Agenda for Future Research.

Comi AM, Sahin M, Hammill A, Kaplan EH, Juhász C, North P, Ball KL, Levin AV, Cohen B, Morris J, Lo W, Roach ES; 2015 Sturge-Weber Syndrome Research Workshop.

Pediatr Neurol. 2016 May;58:12-24. doi: 10.1016/j.pediatrneurol.2015.11.009. Epub 2016 Mar 16.

PMID:
27268758
6.

Trifluorosubstrates as mechanistic probes for an FMN-dependent l-2-hydroxy acid-oxidizing enzyme.

Lederer F, Vignaud C, North P, Bodevin S.

Biochim Biophys Acta. 2016 Sep;1864(9):1215-21. doi: 10.1016/j.bbapap.2016.05.001. Epub 2016 May 4.

PMID:
27155230
7.

Vascular Actions of Angiotensin 1-7 in the Human Microcirculation: Novel Role for Telomerase.

Durand MJ, Zinkevich NS, Riedel M, Gutterman DD, Nasci VL, Salato VK, Hijjawi JB, Reuben CF, North PE, Beyer AM.

Arterioscler Thromb Vasc Biol. 2016 Jun;36(6):1254-62. doi: 10.1161/ATVBAHA.116.307518. Epub 2016 Apr 14.

8.

Morton et al. reply.

Morton DC, Nagol J, Carabajal CC, Rosette J, Palace M, Cook BD, Vermote EF, Harding DJ, North PR.

Nature. 2016 Mar 17;531(7594):E6. doi: 10.1038/nature16458. No abstract available.

PMID:
26983545
9.

Nogo-B receptor deficiency causes cerebral vasculature defects during embryonic development in mice.

Rana U, Liu Z, Kumar SN, Zhao B, Hu W, Bordas M, Cossette S, Szabo S, Foeckler J, Weiler H, Chrzanowska-Wodnicka M, Holtz ML, Misra RP, Salato V, North PE, Ramchandran R, Miao QR.

Dev Biol. 2016 Feb 15;410(2):190-201. doi: 10.1016/j.ydbio.2015.12.023. Epub 2015 Dec 31.

10.

MLL-Rearranged Acute Lymphoblastic Leukemias Activate BCL-2 through H3K79 Methylation and Are Sensitive to the BCL-2-Specific Antagonist ABT-199.

Benito JM, Godfrey L, Kojima K, Hogdal L, Wunderlich M, Geng H, Marzo I, Harutyunyan KG, Golfman L, North P, Kerry J, Ballabio E, Chonghaile TN, Gonzalo O, Qiu Y, Jeremias I, Debose L, O'Brien E, Ma H, Zhou P, Jacamo R, Park E, Coombes KR, Zhang N, Thomas DA, O'Brien S, Kantarjian HM, Leverson JD, Kornblau SM, Andreeff M, Müschen M, Zweidler-McKay PA, Mulloy JC, Letai A, Milne TA, Konopleva M.

Cell Rep. 2015 Dec 29;13(12):2715-27. doi: 10.1016/j.celrep.2015.12.003. Epub 2015 Dec 17.

11.

Venous malformation of the ethmoid and sphenoid sinuses.

Gertel AJ, Southwood JE, North PE, Poetker DM, Loehrl TA.

Am J Otolaryngol. 2016 Jan-Feb;37(1):12-6. doi: 10.1016/j.amjoto.2015.09.008. Epub 2015 Sep 10. Review.

PMID:
26700252
12.

A Protein Kinase C Phosphorylation Motif in GLUT1 Affects Glucose Transport and is Mutated in GLUT1 Deficiency Syndrome.

Lee EE, Ma J, Sacharidou A, Mi W, Salato VK, Nguyen N, Jiang Y, Pascual JM, North PE, Shaul PW, Mettlen M, Wang RC.

Mol Cell. 2015 Jun 4;58(5):845-53. doi: 10.1016/j.molcel.2015.04.015. Epub 2015 May 14.

13.

CXM: a new tool for mapping breast cancer risk in the tumor microenvironment.

Flister MJ, Endres BT, Rudemiller N, Sarkis AB, Santarriaga S, Roy I, Lemke A, Geurts AM, Moreno C, Ran S, Tsaih SW, De Pons J, Carlson DF, Tan W, Fahrenkrug SC, Lazarova Z, Lazar J, North PE, LaViolette PS, Dwinell MB, Shull JD, Jacob HJ.

Cancer Res. 2014 Nov 15;74(22):6419-29. doi: 10.1158/0008-5472.CAN-13-3212. Epub 2014 Aug 29.

14.

De novo expression of sodium-glucose cotransporter SGLT2 in Bowman's capsule coincides with replacement of parietal epithelial cell layer with proximal tubule-like epithelium.

Tabatabai NM, North PE, Regner KR, Kumar SN, Duris CB, Blodgett AB.

J Membr Biol. 2014 Aug;247(8):675-83. doi: 10.1007/s00232-014-9686-4. Epub 2014 Jun 7.

15.

Amazon forests maintain consistent canopy structure and greenness during the dry season.

Morton DC, Nagol J, Carabajal CC, Rosette J, Palace M, Cook BD, Vermote EF, Harding DJ, North PR.

Nature. 2014 Feb 13;506(7487):221-4. doi: 10.1038/nature13006. Epub 2014 Feb 5.

PMID:
24499816
16.

Expression of NgBR is highly associated with estrogen receptor alpha and survivin in breast cancer.

Wang B, Zhao B, North P, Kong A, Huang J, Miao QR.

PLoS One. 2013 Nov 4;8(11):e78083. doi: 10.1371/journal.pone.0078083. eCollection 2013.

17.

Congenital cardiac, aortic arch, and vascular bed anomalies in PHACE syndrome (from the International PHACE Syndrome Registry).

Bayer ML, Frommelt PC, Blei F, Breur JM, Cordisco MR, Frieden IJ, Goddard DS, Holland KE, Krol AL, Maheshwari M, Metry DW, Morel KD, North PE, Pope E, Shieh JT, Southern JF, Wargon O, Siegel DH, Drolet BA.

Am J Cardiol. 2013 Dec 15;112(12):1948-52. doi: 10.1016/j.amjcard.2013.08.025. Epub 2013 Sep 28.

18.

Genomics in clinical practice: lessons from the front lines.

Jacob HJ, Abrams K, Bick DP, Brodie K, Dimmock DP, Farrell M, Geurts J, Harris J, Helbling D, Joers BJ, Kliegman R, Kowalski G, Lazar J, Margolis DA, North P, Northup J, Roquemore-Goins A, Scharer G, Shimoyama M, Strong K, Taylor B, Tsaih SW, Tschannen MR, Veith RL, Wendt-Andrae J, Wilk B, Worthey EA.

Sci Transl Med. 2013 Jul 17;5(194):194cm5. doi: 10.1126/scitranslmed.3006468.

PMID:
23863829
19.

Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ.

Shirley MD, Tang H, Gallione CJ, Baugher JD, Frelin LP, Cohen B, North PE, Marchuk DA, Comi AM, Pevsner J.

N Engl J Med. 2013 May 23;368(21):1971-9. doi: 10.1056/NEJMoa1213507. Epub 2013 May 8.

20.

C560Rβ3 caused platelet integrin αII b β3 to bind fibrinogen continuously, but resulted in a severe bleeding syndrome and increased murine mortality.

Fang J, Nurden P, North P, Nurden AT, Du LM, Valentin N, Wilcox DA.

J Thromb Haemost. 2013 Jun;11(6):1163-71. doi: 10.1111/jth.12209.

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