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Items: 18

1.

An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease.

Mäkeläinen S, Gòdia M, Hellsand M, Viluma A, Hahn D, Makdoumi K, Zeiss CJ, Mellersh C, Ricketts SL, Narfström K, Hallböök F, Ekesten B, Andersson G, Bergström TF.

PLoS Genet. 2019 Mar 19;15(3):e1007873. doi: 10.1371/journal.pgen.1007873. eCollection 2019 Mar.

2.

Resistance to pyrantel embonate and efficacy of fenbendazole in Parascaris univalens on Swedish stud farms.

Martin F, Höglund J, Bergström TF, Karlsson Lindsjö O, Tydén E.

Vet Parasitol. 2018 Dec 15;264:69-73. doi: 10.1016/j.vetpar.2018.11.003. Epub 2018 Nov 10.

3.

Genomic structure of the horse major histocompatibility complex class II region resolved using PacBio long-read sequencing technology.

Viļuma A, Mikko S, Hahn D, Skow L, Andersson G, Bergström TF.

Sci Rep. 2017 Mar 31;7:45518. doi: 10.1038/srep45518.

4.

Whole-Genome Sequencing of a Canine Family Trio Reveals a FAM83G Variant Associated with Hereditary Footpad Hyperkeratosis.

Sayyab S, Viluma A, Bergvall K, Brunberg E, Jagannathan V, Leeb T, Andersson G, Bergström TF.

G3 (Bethesda). 2016 Jan 8;6(3):521-7. doi: 10.1534/g3.115.025643.

5.

Evaluation of whole-genome sequencing of four Chinese crested dogs for variant detection using the ion proton system.

Viluma A, Sayyab S, Mikko S, Andersson G, Bergström TF.

Canine Genet Epidemiol. 2015 Oct 8;2:16. doi: 10.1186/s40575-015-0029-2. eCollection 2015.

6.

Assessment of hereditary retinal degeneration in the English springer spaniel dog and disease relationship to an RPGRIP1 mutation.

Narfström K, Jeong M, Hyman J, Madsen RW, Bergström TF.

Stem Cells Int. 2012;2012:685901. doi: 10.1155/2012/685901. Epub 2012 Feb 28.

7.

Genome-wide analysis of chimpanzee genes with premature termination codons.

Wetterbom A, Gyllensten U, Cavelier L, Bergström TF.

BMC Genomics. 2009 Jan 29;10:56. doi: 10.1186/1471-2164-10-56.

8.

Full-length sequence analysis of the HLA-DRB1 locus suggests a recent origin of alleles.

von Salomé J, Gyllensten U, Bergström TF.

Immunogenetics. 2007 Apr;59(4):261-71. Epub 2007 Feb 16.

PMID:
17345114
9.

Comparative genomic analysis of human and chimpanzee indicates a key role for indels in primate evolution.

Wetterbom A, Sevov M, Cavelier L, Bergström TF.

J Mol Evol. 2006 Nov;63(5):682-90. Epub 2006 Oct 29.

PMID:
17075697
10.

The genetic contribution to canine personality.

Saetre P, Strandberg E, Sundgren PE, Pettersson U, Jazin E, Bergström TF.

Genes Brain Behav. 2006 Apr;5(3):240-8.

11.

Genome-wide prediction of human VNTRs.

Näslund K, Saetre P, von Salomé J, Bergström TF, Jareborg N, Jazin E.

Genomics. 2005 Jan;85(1):24-35.

PMID:
15607419
12.

From wild wolf to domestic dog: gene expression changes in the brain.

Saetre P, Lindberg J, Leonard JA, Olsson K, Pettersson U, Ellegren H, Bergström TF, Vilà C, Jazin E.

Brain Res Mol Brain Res. 2004 Jul 26;126(2):198-206.

PMID:
15249144
13.

Tracing the origin of HLA-DRB1 alleles by microsatellite polymorphism.

Bergström TF, Engkvist H, Erlandsson R, Josefsson A, Mack SJ, Erlich HA, Gyllensten U.

Am J Hum Genet. 1999 Jun;64(6):1709-18.

14.

Phylogenetic history of hominoid DRB loci and alleles inferred from intron sequences.

Bergström TF, Erlandsson R, Engkvist H, Josefsson A, Erlich HA, Gyllensten U.

Immunol Rev. 1999 Feb;167:351-65.

PMID:
10319273
15.

Recent origin of HLA-DRB1 alleles and implications for human evolution.

Bergström TF, Josefsson A, Erlich HA, Gyllensten U.

Nat Genet. 1998 Mar;18(3):237-42.

PMID:
9500545
16.

Analysis of intron sequences at the class II HLA-DRB1 locus: implications for the age of allelic diversity.

Bergström TF, Josefsson A, Erlich HA, Gyllensten UB.

Hereditas. 1997;127(1-2):1-5.

17.

HLA Sequence Polymorphism and the Origin of Humans.

Erlich HA, Bergström TF, Stoneking M, Gyllensten U.

Science. 1996 Nov 29;274(5292):1552b-4b. No abstract available.

PMID:
17817004
18.

HLA sequence polymorphism and the origin of humans.

Erlich HA, Bergström TF, Stoneking M, Gyllensten U.

Science. 1996 Nov 29;274(5292):1552-4. No abstract available.

PMID:
8966622

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