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Papers authored by Bryda EC

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A Restriction Enzyme-PCR-Based Technique to Determine Transgene Insertion Sites.

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Bryda EC and Bauer BA

Methods in molecular biology (Clifton, N.J.) 597:287-99, 2010 - Who cited this? | PubMed ID: 20013241 | Fulltext

Mutational Insertion of a ROSA26-EGFP Transgene Leads to Defects in Spermiogenesis and Male Infertility in Mice.

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Walters EM, Bauer BA, Franklin CL, Evans TJ, Bryda EC, Riley LK, and Critser JK

Comparative medicine 59(6):545-52, 2009 Dec - Who cited this? | PubMed ID: 20034429 | Fulltext

The polycystic kidney disease-related proteins Bicc1 and SamCystin interact.

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Stagner EE, Bouvrette DJ, Cheng J, and Bryda EC

Biochemical and biophysical research communications 383(1):16-21, 2009 May 22 - Who cited this? | PubMed ID: 19324013 | Fulltext

FRET analysis of actin-myosin interaction in contracting rat aortic smooth muscle.

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Black J, Dykes A, Thatcher S, Brown D, Bryda EC, and Wright GL

Canadian journal of physiology and pharmacology 87(5):327-36, 2009 May - Who cited this? | PubMed ID: 19448730 | Fulltext

Multiplex microsatellite marker panels for genetic monitoring of common rat strains.

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Bryda EC and Riley AL

Journal of the American Association for Laboratory Animal Science : JAALAS 47(3):37-41, 2008 May - Who cited this? | PubMed ID: 18459711 | Fulltext

K homology domains of the mouse polycystic kidney disease-related protein, Bicaudal-C (Bicc1), mediate RNA binding in vitro.

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Bouvrette DJ, Price SJ, and Bryda EC

Nephron. Experimental nephrology 108(1):e27-34, 2008 - Who cited this? | PubMed ID: 18182784 | Fulltext

Breeding colony refinement through phenotypic and genotypic characterization of the SPRD-Pkdr1/Rrrc rat model of polycystic kidney disease.

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Bauer BA, Boedges S, Cook CR, Bryda EC, and Franklin CL

Comparative medicine 57(2):193-9, 2007 Apr - Who cited this? | PubMed ID: 17536620 | Fulltext

Method for detection and identification of multiple chromosomal integration sites in transgenic animals created with lentivirus.

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Bryda EC, Pearson M, Agca Y, and Bauer BA

BioTechniques 41(6):715-9, 2006 Dec - Who cited this? | PubMed ID: 17191616 | Fulltext

Detection of histidine decarboxylase in rat aorta and cultured rat aortic smooth muscle cells.

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Tippens AS, Davis SV, Hayes JR, Bryda EC, Green TL, and Gruetter CA

Inflammation research : official journal of the European Histamine Research Society ... [et al.] 53(8):390-5, 2004 Aug - Who cited this? | PubMed ID: 15316670 | Fulltext

Effect of experimental hyperhomocysteinemia on cardiac structure and function in the rat.

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Walker E, Black J, Parris C, Bryda EC, Cansino S, Hunt L, Chappell J, Wehner P, Studeny M, and Wright GL

Annals of clinical and laboratory science 34(2):175-80, 2004 - Who cited this? | PubMed ID: 15228230 | Fulltext

Positional cloning of jcpk/bpk locus of the mouse.

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Cogswell C, Price SJ, Hou X, Guay-Woodford LM, Flaherty L, and Bryda EC

Mammalian genome : official journal of the International Mammalian Genome Society 14(4):242-9, 2003 Apr - Who cited this? | PubMed ID: 12682776 | Fulltext

A new mouse model for autosomal recessive polycystic kidney disease.

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Chittenden L, Lu X, Cacheiro NL, Cain KT, Generoso W, Bryda EC, and Stubbs L

Genomics 79(4):499-504, 2002 Apr - Who cited this? | PubMed ID: 11944981 | Fulltext

Characterization of the region containing the jcpk PKD gene on mouse Chromosome 10.

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Price SJ, Chittenden LR, Flaherty L, O'Dell B, Guay-Woodford LM, Stubbs L, and Bryda EC

Cytogenetic and genome research 98(1):61-6, 2002 - Who cited this? | PubMed ID: 12584442 | Fulltext

High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v).

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Bryda EC, Kim HJ, Legare ME, Frankel WN, and Noben-Trauth K

Genomics 73(3):338-42, 2001 May 1 - Who cited this? | PubMed ID: 11350126 | Fulltext

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.

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Di Palma F, Holme RH, Bryda EC, Belyantseva IA, Pellegrino R, Kachar B, Steel KP, and Noben-Trauth K

Nature genetics 27(1):103-7, 2001 Jan - Who cited this? | PubMed ID: 11138008 | Fulltext

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.

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Bolz H, von Brederlow B, Ramírez A, Bryda EC, Kutsche K, Nothwang HG, Seeliger M, del C-Salcedó Cabrera M, Vila MC, Molina OP, Gal A, and Kubisch C

Nature genetics 27(1):108-12, 2001 Jan - Who cited this? | PubMed ID: 11138009 | Fulltext

Mouse chromosome 10.

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Burmeister M, Bryda EC, Bureau JF, and Noben-Trauth K

Mammalian genome : official journal of the International Mammalian Genome Society 10(10):950-1, 1999 Oct - Who cited this? | PubMed ID: 10501952 | Fulltext

Scraggly, a new hair loss mutation on mouse chromosome 19.

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Herron BJ, Bryda EC, Heverly SA, Collins DN, and Flaherty L

Mammalian genome : official journal of the International Mammalian Genome Society 10(9):864-9, 1999 Sep - Who cited this? | PubMed ID: 10441736 | Fulltext

Encyclopedia of the mouse genome VII. Mouse chromosome 10.

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Burmeister M, Bryda EC, Bureau JF, and Noben-Trauth K

Mammalian genome : official journal of the International Mammalian Genome Society 8 Spec No:S200-14, 1998 - Who cited this? | PubMed ID: 9662627 | Fulltext

A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer.

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Bryda EC, Ling H, and Flaherty L

Mammalian genome : official journal of the International Mammalian Genome Society 8(1):1-4, 1997 Jan - Who cited this? | PubMed ID: 9021139 | Fulltext

Mouse chromosome 10.

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Taylor BA, Burmeister M, and Bryda EC

Mammalian genome : official journal of the International Mammalian Genome Society 7 Spec No:S176-89, 1997 - Who cited this? | PubMed ID: 9233393 | Fulltext

Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic.

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Guay-Woodford LM, Bryda EC, Christine B, Lindsey JR, Collier WR, Avner ED, D'Eustachio P, and Flaherty L

Kidney international 50(4):1158-65, 1996 Oct - Who cited this? | PubMed ID: 8887273 | Fulltext

Fine genetic map of mouse chromosome 10 around the polycystic kidney disease gene, jcpk, and ankyrin 3.

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Bryda EC, Ling H, Rathbun DE, Burmeister M, and Flaherty L

Genomics 35(3):425-30, 1996 Aug 1 - Who cited this? | PubMed ID: 8812475 | Fulltext

Recovery of probes linked to the jcpk locus on mouse chromosome 10 by the use of an improved representational difference analysis technique.

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Baldocchi RA, Tartaglia KE, Bryda EC, and Flaherty L

Genomics 33(2):193-8, 1996 Apr 15 - Who cited this? | PubMed ID: 8660967 | Fulltext

Encyclopedia of the mouse genome V. Mouse chromosome 10.

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Taylor BA, Burmeister M, and Bryda EC

Mammalian genome : official journal of the International Mammalian Genome Society 6 Spec No:S190-200, 1996 - Who cited this? | PubMed ID: 8800764 | Fulltext

New mouse model for polycystic kidney disease with both recessive and dominant gene effects.

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Flaherty L, Bryda EC, Collins D, Rudofsky U, and Montogomery JC

Kidney international 47(2):552-8, 1995 Feb - Who cited this? | PubMed ID: 7723240 | Fulltext

Mouse chromosome 10.

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Taylor BA, Burmeister M, and Bryda EC

Mammalian genome : official journal of the International Mammalian Genome Society 5 Spec No:S154-63, 1994 - Who cited this? | PubMed ID: 7719003 | Fulltext

Multiple sites of crossing over within the Eb recombinational hotspot in the mouse.

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Bryda EC, DePari JA, Sant'Angelo DB, Murphy DB, and Passmore HC

Mammalian genome : official journal of the International Mammalian Genome Society 2(2):123-9, 1992 - Who cited this? | PubMed ID: 1347471 | Fulltext

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