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Items: 1 to 50 of 118

1.

Effectiveness of the IBCLC: Have we Made an Impact on the Care of Breastfeeding Families Over the Past Decade?

Haase B, Brennan E, Wagner CL.

J Hum Lact. 2019 Jun 17:890334419851805. doi: 10.1177/0890334419851805. [Epub ahead of print]

PMID:
31206324
2.

The Burmese cat as a genetic model of type 2 diabetes in humans.

Samaha G, Beatty J, Wade CM, Haase B.

Anim Genet. 2019 Jun 10. doi: 10.1111/age.12799. [Epub ahead of print] Review.

PMID:
31179570
3.

Genomic Characterization of External Morphology Traits in Kelpies Does Not Support Common Ancestry with the Australian Dingo.

Chew T, Willet CE, Haase B, Wade CM.

Genes (Basel). 2019 May 3;10(5). pii: E337. doi: 10.3390/genes10050337.

4.

Breed-specific variations in the coding region of toll-like receptor 4 in the domestic cat.

Whitney J, Haase B, Beatty J, Barrs VR.

Vet Immunol Immunopathol. 2019 Mar;209:61-69. doi: 10.1016/j.vetimm.2019.02.009. Epub 2019 Feb 26.

PMID:
30885307
5.

Spontaneous parametric down-conversion of photons at 660 nm to the terahertz and sub-terahertz frequency range.

Haase B, Kutas M, Riexinger F, Bickert P, Keil A, Molter D, Bortz M, von Freymann G.

Opt Express. 2019 Mar 4;27(5):7458-7468. doi: 10.1364/OE.27.007458.

PMID:
30876309
6.

Author Correction: Applications and efficiencies of the first cat 63 K DNA array.

Gandolfi B, Alhaddad H, Abdi M, Bach LH, Creighton EK, Davis BW, Decker JE, Dodman NH, Ginns EI, Grahn JC, Grahn RA, Haase B, Haggstrom J, Hamilton MJ, Helps CR, Kurushima JD, Lohi H, Longeri M, Malik R, Meurs KM, Montague MJ, Mullikin JC, Murphy WJ, Nilson SM, Pedersen NC, Peterson CB, Rusbridge C, Saif R, Shelton GD, Warren WC, Wasim M, Lyons LA.

Sci Rep. 2019 Mar 12;9(1):4664. doi: 10.1038/s41598-018-38073-6.

7.

Designing Longitudinal Clinical Studies Involving Lactating Women.

Wagner CL, Taylor SN, Haase B.

J Hum Lact. 2019 Feb;35(1):32-36. doi: 10.1177/0890334418812362. Epub 2018 Nov 27.

PMID:
30481481
8.

Single-cell isoform RNA sequencing characterizes isoforms in thousands of cerebellar cells.

Gupta I, Collier PG, Haase B, Mahfouz A, Joglekar A, Floyd T, Koopmans F, Barres B, Smit AB, Sloan SA, Luo W, Fedrigo O, Ross ME, Tilgner HU.

Nat Biotechnol. 2018 Oct 15. doi: 10.1038/nbt.4259. [Epub ahead of print]

PMID:
30320766
9.

Facilitating Colostrum Collection by Hospitalized Women in the Early Postpartum Period for Infant Trophic Feeding and Oral Immune Therapy.

Haase B, Johnson TS, Wagner CL.

J Obstet Gynecol Neonatal Nurs. 2018 Sep;47(5):654-660. doi: 10.1016/j.jogn.2018.05.003. Epub 2018 Jul 2.

PMID:
30196807
10.

Author Correction: Applications and efficiencies of the first cat 63K DNA array.

Gandolfi B, Alhaddad H, Abdi M, Bach LH, Creighton EK, Davis BW, Decker JE, Dodman NH, Ginns EI, Grahn JC, Grahn RA, Haase B, Haggstrom J, Hamilton MJ, Helps CR, Kurushima JD, Lohi H, Longeri M, Malik R, Meurs KM, Montague MJ, Mullikin JC, Murphy WJ, Nilson SM, Pedersen NC, Peterson CB, Rusbridge C, Saif R, Shelton GD, Warren WC, Wasim M, Lyons LA.

Sci Rep. 2018 Jun 4;8(1):8746. doi: 10.1038/s41598-018-26885-5.

11.

Applications and efficiencies of the first cat 63K DNA array.

Gandolfi B, Alhaddad H, Abdi M, Bach LH, Creighton EK, Davis BW, Decker JE, Dodman NH, Ginns EI, Grahn JC, Grahn RA, Haase B, Haggstrom J, Hamilton MJ, Helps CR, Kurushima JD, Lohi H, Longeri M, Malik R, Meurs KM, Montague MJ, Mullikin JC, Murphy WJ, Nilson SM, Pedersen NC, Peterson CB, Rusbridge C, Saif R, Shelton GD, Warren WC, Wasim M, Lyons LA.

Sci Rep. 2018 May 4;8(1):7024. doi: 10.1038/s41598-018-25438-0. Erratum in: Sci Rep. 2018 Jun 4;8(1):8746. Sci Rep. 2019 Mar 12;9(1):4664.

12.

Novel KIT variants for dominant white in the Australian horse population.

Hoban R, Castle K, Hamilton N, Haase B.

Anim Genet. 2018 Feb;49(1):99-100. doi: 10.1111/age.12627. Epub 2018 Jan 15. No abstract available.

PMID:
29333746
13.

A miRNA181a/NFAT5 axis links impaired T cell tolerance induction with autoimmune type 1 diabetes.

Serr I, Scherm MG, Zahm AM, Schug J, Flynn VK, Hippich M, Kälin S, Becker M, Achenbach P, Nikolaev A, Gerlach K, Liebsch N, Loretz B, Lehr CM, Kirchner B, Spornraft M, Haase B, Segars J, Küper C, Palmisano R, Waisman A, Willis RA, Kim WU, Weigmann B, Kaestner KH, Ziegler AG, Daniel C.

Sci Transl Med. 2018 Jan 3;10(422). pii: eaag1782. doi: 10.1126/scitranslmed.aag1782. Erratum in: Sci Transl Med. 2019 Feb 20;11(480):.

14.

The effect of differing kidney disease treatment modalities and organ donation and transplantation practices on health expenditure and patient outcomes.

Jager KJ, Stel VS, Branger P, Guijt M, Busic M, Dragovic M, Diekmann F, Manyalich M, Di Ciaccio P, Nanni Costa A, Collett D, Mumford L, Haase B, Hemke A, Deme O, Mihály S, Murphy M, Couchoud C, Massy Z, Lingemann M, Rahmel A.

Nephrol Dial Transplant. 2018 Apr 1;33(4):560-562. doi: 10.1093/ndt/gfx082.

PMID:
29106604
15.

Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds.

Schaefer RJ, Schubert M, Bailey E, Bannasch DL, Barrey E, Bar-Gal GK, Brem G, Brooks SA, Distl O, Fries R, Finno CJ, Gerber V, Haase B, Jagannathan V, Kalbfleisch T, Leeb T, Lindgren G, Lopes MS, Mach N, da Câmara Machado A, MacLeod JN, McCoy A, Metzger J, Penedo C, Polani S, Rieder S, Tammen I, Tetens J, Thaller G, Verini-Supplizi A, Wade CM, Wallner B, Orlando L, Mickelson JR, McCue ME.

BMC Genomics. 2017 Jul 27;18(1):565. doi: 10.1186/s12864-017-3943-8.

16.

A Coding Variant in the Gene Bardet-Biedl Syndrome 4 (BBS4) Is Associated with a Novel Form of Canine Progressive Retinal Atrophy.

Chew T, Haase B, Bathgate R, Willet CE, Kaukonen MK, Mascord LJ, Lohi HT, Wade CM.

G3 (Bethesda). 2017 Jul 5;7(7):2327-2335. doi: 10.1534/g3.117.043109.

17.

Exclusion of known progressive retinal atrophy genes for blindness in the Hungarian Puli.

Chew T, Haase B, Willet CE, Wade CM.

Anim Genet. 2017 Aug;48(4):500-501. doi: 10.1111/age.12553. Epub 2017 Apr 5. No abstract available.

PMID:
28378943
18.

Identification of MiR-21-5p as a Functional Regulator of Mesothelin Expression Using MicroRNA Capture Affinity Coupled with Next Generation Sequencing.

De Santi C, Vencken S, Blake J, Haase B, Benes V, Gemignani F, Landi S, Greene CM.

PLoS One. 2017 Jan 26;12(1):e0170999. doi: 10.1371/journal.pone.0170999. eCollection 2017.

19.

Conscious Leadership.

Ward SF, Haase B.

AORN J. 2016 Nov;104(5):433.e1-433.e9. doi: 10.1016/j.aorn.2016.09.002.

PMID:
27793254
20.

miRNA92a targets KLF2 and the phosphatase PTEN signaling to promote human T follicular helper precursors in T1D islet autoimmunity.

Serr I, Fürst RW, Ott VB, Scherm MG, Nikolaev A, Gökmen F, Kälin S, Zillmer S, Bunk M, Weigmann B, Kunschke N, Loretz B, Lehr CM, Kirchner B, Haase B, Pfaffl M, Waisman A, Willis RA, Ziegler AG, Daniel C.

Proc Natl Acad Sci U S A. 2016 Oct 25;113(43):E6659-E6668. Epub 2016 Oct 10. Erratum in: Proc Natl Acad Sci U S A. 2018 Apr 16;:.

21.

Family Over Rules? An Ethical Analysis of Allowing Families to Overrule Donation Intentions.

Shaw D, Georgieva D, Haase B, Gardiner D, Lewis P, Jansen N, Wind T, Samuel U, McDonald M, Ploeg R; ELPAT Working Group on Deceased Donation.

Transplantation. 2017 Mar;101(3):482-487. doi: 10.1097/TP.0000000000001536. Review.

PMID:
27764030
22.

Validation of a candidate causative mutation for white spotting in donkeys.

Fenn DJ, Raudsepp T, Cothran EG, Hamilton NA, Haase B.

Anim Genet. 2017 Feb;48(1):124-125. doi: 10.1111/age.12494. Epub 2016 Sep 9. No abstract available.

PMID:
27611565
23.

The differential expression of alternatively polyadenylated transcripts is a common stress-induced response mechanism that modulates mammalian mRNA expression in a quantitative and qualitative fashion.

Hollerer I, Curk T, Haase B, Benes V, Hauer C, Neu-Yilik G, Bhuvanagiri M, Hentze MW, Kulozik AE.

RNA. 2016 Sep;22(9):1441-53. doi: 10.1261/rna.055657.115. Epub 2016 Jul 12.

24.

The Slicer Activity of ARGONAUTE1 Is Required Specifically for the Phasing, Not Production, of Trans-Acting Short Interfering RNAs in Arabidopsis.

Arribas-Hernández L, Marchais A, Poulsen C, Haase B, Hauptmann J, Benes V, Meister G, Brodersen P.

Plant Cell. 2016 Jul;28(7):1563-80. doi: 10.1105/tpc.16.00121. Epub 2016 Jun 27.

25.

Digging for known genetic mutations underlying inherited bone and cartilage characteristics and disorders in the dog and cat.

Haase B, Mazrier H, Wade CM.

Vet Comp Orthop Traumatol. 2016 Jul 19;29(4):269-76. doi: 10.3415/VCOT-16-02-0037. Epub 2016 May 18. Review.

PMID:
27189647
26.

Inheritance of chronic superficial keratitis in Australian Greyhounds.

Cheng S, Wigney D, Haase B, Wade CM.

Anim Genet. 2016 Oct;47(5):629. doi: 10.1111/age.12446. Epub 2016 May 5. No abstract available.

PMID:
27147552
27.

A dominant TRPV4 variant underlies osteochondrodysplasia in Scottish fold cats.

Gandolfi B, Alamri S, Darby WG, Adhikari B, Lattimer JC, Malik R, Wade CM, Lyons LA, Cheng J, Bateman JF, McIntyre P, Lamandé SR, Haase B.

Osteoarthritis Cartilage. 2016 Aug;24(8):1441-50. doi: 10.1016/j.joca.2016.03.019. Epub 2016 Apr 6.

28.

Erratum to: Evidence of selection signatures that shape the Persian cat breed.

Bertolini F, Gandolfi B, Kim ES, Haase B, Lyons LA, Rothschild MF.

Mamm Genome. 2016 Apr;27(3-4):156-7. doi: 10.1007/s00335-016-9626-y. No abstract available.

PMID:
27007993
29.

Evidence of selection signatures that shape the Persian cat breed.

Bertolini F, Gandolfi B, Kim ES, Haase B, Lyons LA, Rothschild MF.

Mamm Genome. 2016 Apr;27(3-4):144-55. doi: 10.1007/s00335-016-9623-1. Epub 2016 Mar 8. Erratum in: Mamm Genome. 2016 Apr;27(3-4):156-7.

PMID:
26956354
30.

Domperidone for Treatment of Low Milk Supply in Breast Pump-Dependent Mothers of Hospitalized Premature Infants: A Clinical Protocol.

Haase B, Taylor SN, Mauldin J, Johnson TS, Wagner CL.

J Hum Lact. 2016 May;32(2):373-81. doi: 10.1177/0890334416630539. Epub 2016 Feb 23.

PMID:
26905341
31.

Decreased Fronto-Limbic Activation and Disrupted Semantic-Cued List Learning in Major Depressive Disorder.

Kassel MT, Rao JA, Walker SJ, Briceño EM, Gabriel LB, Weldon AL, Avery ET, Haase BD, Peciña M, Considine CM, Noll DC, Bieliauskas LA, Starkman MN, Zubieta JK, Welsh RC, Giordani B, Weisenbach SL, Langenecker SA.

J Int Neuropsychol Soc. 2016 Apr;22(4):412-25. doi: 10.1017/S1355617716000023. Epub 2016 Feb 2.

32.

Ethical, legal, and societal issues and recommendations for controlled and uncontrolled DCD.

Haase B, Bos M, Boffa C, Lewis P, Rudge C, Valero R, Wind T, Wright L.

Transpl Int. 2016 Jul;29(7):771-9. doi: 10.1111/tri.12720. Epub 2016 Jan 13. Review.

33.

Strong selection for behavioural resilience in Australian stock working dogs identified by selective sweep analysis.

Arnott ER, Peek L, Early JB, Pan AY, Haase B, Chew T, McGreevy PD, Wade CM.

Canine Genet Epidemiol. 2015 May 7;2:6. doi: 10.1186/s40575-015-0017-6. eCollection 2015.

34.

A novel KIT variant in an Icelandic horse with white-spotted coat colour.

Haase B, Jagannathan V, Rieder S, Leeb T.

Anim Genet. 2015 Aug;46(4):466. doi: 10.1111/age.12313. Epub 2015 Jun 9. No abstract available.

PMID:
26059442
35.

Stress Response to the Functional Magnetic Resonance Imaging Environment in Healthy Adults Relates to the Degree of Limbic Reactivity during Emotion Processing.

Weldon AL, Hagan M, Van Meter A, Jacobs RH, Kassel MT, Hazlett KE, Haase BD, Vederman AC, Avery E, Briceno EM, Welsh RC, Zubieta JK, Weisenbach SL, Langenecker SA.

Neuropsychobiology. 2015;71(2):85-96. Epub 2015 Apr 9.

PMID:
25871424
36.

Two variants in the KIT gene as candidate causative mutations for a dominant white and a white spotting phenotype in the donkey.

Haase B, Rieder S, Leeb T.

Anim Genet. 2015 Jun;46(3):321-4. doi: 10.1111/age.12282. Epub 2015 Mar 27.

PMID:
25818843
37.

X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene.

Shelton GD, Rider BE, Child G, Tzannes S, Guo LT, Moghadaszadeh B, Troiano EC, Haase B, Wade CM, Beggs AH.

Skelet Muscle. 2015 Jan 27;5(1):1. doi: 10.1186/s13395-014-0025-3. eCollection 2015.

38.

Canine disorder mirrors human disease: exonic deletion in HES7 causes autosomal recessive spondylocostal dysostosis in miniature Schnauzer dogs.

Willet CE, Makara M, Reppas G, Tsoukalas G, Malik R, Haase B, Wade CM.

PLoS One. 2015 Feb 6;10(2):e0117055. doi: 10.1371/journal.pone.0117055. eCollection 2015.

39.

Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker.

Willet CE, Haase B, Charleston MA, Wade CM.

Bioinformatics. 2015 Feb 15;31(4):599-601. doi: 10.1093/bioinformatics/btu691. Epub 2014 Oct 21.

40.

Optimization of extraction of circulating RNAs from plasma--enabling small RNA sequencing.

Spornraft M, Kirchner B, Haase B, Benes V, Pfaffl MW, Riedmaier I.

PLoS One. 2014 Sep 17;9(9):e107259. doi: 10.1371/journal.pone.0107259. eCollection 2014.

41.
42.

An updated felCat5 SNP manifest for the Illumina Feline 63k SNP genotyping array.

Willet CE, Haase B.

Anim Genet. 2014 Aug;45(4):614-5. doi: 10.1111/age.12169. Epub 2014 May 7. No abstract available.

PMID:
24804964
43.

Sequencing of a patient with balanced chromosome abnormalities and neurodevelopmental disease identifies disruption of multiple high risk loci by structural variation.

Blake J, Riddell A, Theiss S, Gonzalez AP, Haase B, Jauch A, Janssen JW, Ibberson D, Pavlinic D, Moog U, Benes V, Runz H.

PLoS One. 2014 Mar 13;9(3):e90894. doi: 10.1371/journal.pone.0090894. eCollection 2014.

44.

Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse.

Bellone RR, Holl H, Setaluri V, Devi S, Maddodi N, Archer S, Sandmeyer L, Ludwig A, Foerster D, Pruvost M, Reissmann M, Bortfeldt R, Adelson DL, Lim SL, Nelson J, Haase B, Engensteiner M, Leeb T, Forsyth G, Mienaltowski MJ, Mahadevan P, Hofreiter M, Paijmans JL, Gonzalez-Fortes G, Grahn B, Brooks SA.

PLoS One. 2013 Oct 22;8(10):e78280. doi: 10.1371/journal.pone.0078280. eCollection 2013.

45.

Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses.

Haase B, Signer-Hasler H, Binns MM, Obexer-Ruff G, Hauswirth R, Bellone RR, Burger D, Rieder S, Wade CM, Leeb T.

PLoS One. 2013 Sep 30;8(9):e75071. doi: 10.1371/journal.pone.0075071. eCollection 2013.

46.

Excessive supraventricular ectopic activity is indicative of paroxysmal atrial fibrillation in patients with cerebral ischemia.

Weber-Krüger M, Gröschel K, Mende M, Seegers J, Lahno R, Haase B, Niehaus CF, Edelmann F, Hasenfuß G, Wachter R, Stahrenberg R.

PLoS One. 2013 Jun 28;8(6):e67602. doi: 10.1371/journal.pone.0067602. Print 2013.

47.

Broadband homodecoupled NMR spectroscopy with enhanced sensitivity.

Sakhaii P, Haase B, Bermel W, Kerssebaum R, Wagner GE, Zangger K.

J Magn Reson. 2013 Aug;233:92-5. doi: 10.1016/j.jmr.2013.05.008. Epub 2013 May 30.

PMID:
23793056
48.

Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes.

Hauswirth R, Jude R, Haase B, Bellone RR, Archer S, Holl H, Brooks SA, Tozaki T, Penedo MC, Rieder S, Leeb T.

Anim Genet. 2013 Dec;44(6):763-5. doi: 10.1111/age.12057. Epub 2013 May 9.

PMID:
23659293
49.

[Clinical evaluation of the new coat colour macchiato in a male Franches-Montagnes horse].

Blatter M, Haase B, Gerber V, Poncet PA, Leeb T, Rieder S, Henke D, Janett F, Burger D.

Schweiz Arch Tierheilkd. 2013 Apr;155(4):229-32. doi: 10.1024/0036-7281/a000451. German.

50.

Broadband homodecoupled heteronuclear multiple bond correlation spectroscopy.

Sakhaii P, Haase B, Bermel W.

J Magn Reson. 2013 Mar;228:125-9. doi: 10.1016/j.jmr.2012.12.018. Epub 2013 Jan 8.

PMID:
23395829

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