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Items: 1 to 20 of 21


SPECC1L deficiency results in increased adherens junction stability and reduced cranial neural crest cell delamination.

Wilson NR, Olm-Shipman AJ, Acevedo DS, Palaniyandi K, Hall EG, Kosa E, Stumpff KM, Smith GJ, Pitstick L, Liao EC, Bjork BC, Czirok A, Saadi I.

Sci Rep. 2016 Jan 20;6:17735. doi: 10.1038/srep17735.


'Predatory' open access: a longitudinal study of article volumes and market characteristics.

Shen C, Björk BC.

BMC Med. 2015 Oct 1;13:230. doi: 10.1186/s12916-015-0469-2.


Have the "mega-journals" reached the limits to growth?

Björk BC.

PeerJ. 2015 May 26;3:e981. doi: 10.7717/peerj.981. eCollection 2015.


Critical thinking and reflection exercises in a biochemistry course to improve prospective health professions students' attitudes toward physician-pharmacist collaboration.

Van Winkle LJ, Cornell S, Fjortoft N, Bjork BC, Chandar N, Green JM, La Salle S, Viselli SM, Burdick P, Lynch SM.

Am J Pharm Educ. 2013 Oct 14;77(8):169. doi: 10.5688/ajpe778169.


Interprofessional workshop to improve mutual understanding between pharmacy and medical students.

Van Winkle LJ, Bjork BC, Chandar N, Cornell S, Fjortoft N, Green JM, La Salle S, Lynch SM, Viselli SM, Burdick P.

Am J Pharm Educ. 2012 Oct 12;76(8):150. doi: 10.5688/ajpe768150.


Anatomy of open access publishing: a study of longitudinal development and internal structure.

Laakso M, Björk BC.

BMC Med. 2012 Oct 22;10:124. doi: 10.1186/1741-7015-10-124.


Open access versus subscription journals: a comparison of scientific impact.

Björk BC, Solomon D.

BMC Med. 2012 Jul 17;10:73. doi: 10.1186/1741-7015-10-73.


A study of innovative features in scholarly open access journals.

Björk BC.

J Med Internet Res. 2011 Dec 16;13(4):e115. doi: 10.2196/jmir.1802.


The development of open access journal publishing from 1993 to 2009.

Laakso M, Welling P, Bukvova H, Nyman L, Björk BC, Hedlund T.

PLoS One. 2011;6(6):e20961. doi: 10.1371/journal.pone.0020961. Epub 2011 Jun 13.


A transient transgenic RNAi strategy for rapid characterization of gene function during embryonic development.

Bjork BC, Fujiwara Y, Davis SW, Qiu H, Saunders TL, Sandy P, Orkin S, Camper SA, Beier DR.

PLoS One. 2010 Dec 16;5(12):e14375. doi: 10.1371/journal.pone.0014375.


Open access to the scientific journal literature: situation 2009.

Björk BC, Welling P, Laakso M, Majlender P, Hedlund T, Gudnason G.

PLoS One. 2010 Jun 23;5(6):e11273. doi: 10.1371/journal.pone.0011273.


Novel cleft susceptibility genes in chromosome 6q.

Letra A, Menezes R, Fonseca RF, Govil M, McHenry T, Murphy MJ, Hennebold JD, Granjeiro JM, Castilla EE, Orioli IM, Martin R, Marazita ML, Bjork BC, Vieira AR.

J Dent Res. 2010 Sep;89(9):927-32. doi: 10.1177/0022034510370004. Epub 2010 May 28.


Genome-wide identification of mouse congenital heart disease loci.

Kamp A, Peterson MA, Svenson KL, Bjork BC, Hentges KE, Rajapaksha TW, Moran J, Justice MJ, Seidman JG, Seidman CE, Moskowitz IP, Beier DR.

Hum Mol Genet. 2010 Aug 15;19(16):3105-13. doi: 10.1093/hmg/ddq211. Epub 2010 May 28.


Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse.

Stottmann RW, Bjork BC, Doyle JB, Beier DR.

Genesis. 2010 May;48(5):303-8. doi: 10.1002/dvg.20618.


Prdm16 is required for normal palatogenesis in mice.

Bjork BC, Turbe-Doan A, Prysak M, Herron BJ, Beier DR.

Hum Mol Genet. 2010 Mar 1;19(5):774-89. doi: 10.1093/hmg/ddp543. Epub 2009 Dec 11.


SNP2RFLP: a computational tool to facilitate genetic mapping using benchtop analysis of SNPs.

Beckstead WA, Bjork BC, Stottmann RW, Sunyaev S, Beier DR.

Mamm Genome. 2008 Oct-Dec;19(10-12):687-90. doi: 10.1007/s00335-008-9149-2. Epub 2008 Oct 29.


Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

Moran JL, Bolton AD, Tran PV, Brown A, Dwyer ND, Manning DK, Bjork BC, Li C, Montgomery K, Siepka SM, Vitaterna MH, Takahashi JS, Wiltshire T, Kwiatkowski DJ, Kucherlapati R, Beier DR.

Genome Res. 2006 Mar;16(3):436-40. Epub 2006 Feb 3.


Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.

Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, Lidral AC, Pober BR, Moreno L, Arcos-Burgos M, Valencia C, Houdayer C, Bahuau M, Moretti-Ferreira D, Richieri-Costa A, Dixon MJ, Murray JC.

Nat Genet. 2002 Oct;32(2):285-9. Epub 2002 Sep 3.


Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.

Watanabe Y, Murray JC, Bjork BC, Bird CP, Chiang PW, Gregory SG, Kurnit DM, Schutte BC.

Hum Mutat. 2001 Nov;18(5):422-34.


A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.

Schutte BC, Bjork BC, Coppage KB, Malik MI, Gregory SG, Scott DJ, Brentzell LM, Watanabe Y, Dixon MJ, Murray JC.

Genome Res. 2000 Jan;10(1):81-94.

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