Lohi H - Search Results

1

Clinical and Genetic Findings in 28 American Cocker Spaniels with Aural Ceruminous Gland Hyperplasia and Ectasia.

Kaimio M, Malkamäki S, Kaukonen M, Ahonen S, Hytönen MK, Rantala M, Lohi H, Saijonmaa-Koulumies L, Laitinen-Vapaavuori O. Kaimio M, et al. Among authors: lohi h. J Comp Pathol. 2021 May;185:30-44. doi: 10.1016/j.jcpa.2021.03.005. Epub 2021 Apr 22. J Comp Pathol. 2021. PMID: 34119229 Free article.

2

A mutation in hairless dogs implicates FOXI3 in ectodermal development.

Drögemüller C, Karlsson EK, Hytönen MK, Perloski M, Dolf G, Sainio K, Lohi H, Lindblad-Toh K, Leeb T. Drögemüller C, et al. Among authors: lohi h. Science. 2008 Sep 12;321(5895):1462. doi: 10.1126/science.1162525. Science. 2008. PMID: 18787161

3

Ancestral T-box mutation is present in many, but not all, short-tailed dog breeds.

Hytönen MK, Grall A, Hédan B, Dréano S, Seguin SJ, Delattre D, Thomas A, Galibert F, Paulin L, Lohi H, Sainio K, André C. Hytönen MK, et al. Among authors: lohi h. J Hered. 2009 Mar-Apr;100(2):236-40. doi: 10.1093/jhered/esn085. Epub 2008 Oct 14. J Hered. 2009. PMID: 18854372

4

Mutation in HSF4 is associated with hereditary cataract in the Australian Shepherd.

Mellersh CS, McLaughlin B, Ahonen S, Pettitt L, Lohi H, Barnett KC. Mellersh CS, et al. Among authors: lohi h. Vet Ophthalmol. 2009 Nov-Dec;12(6):372-8. doi: 10.1111/j.1463-5224.2009.00735.x. Vet Ophthalmol. 2009. PMID: 19883468

5

An ADAMTS17 splice donor site mutation in dogs with primary lens luxation.

Farias FH, Johnson GS, Taylor JF, Giuliano E, Katz ML, Sanders DN, Schnabel RD, McKay SD, Khan S, Gharahkhani P, O'Leary CA, Pettitt L, Forman OP, Boursnell M, McLaughlin B, Ahonen S, Lohi H, Hernandez-Merino E, Gould DJ, Sargan DR, Mellersh C. Farias FH, et al. Among authors: lohi h. Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4716-21. doi: 10.1167/iovs.09-5142. Epub 2010 Apr 7. Invest Ophthalmol Vis Sci. 2010. PMID: 20375329

6

Assessment of canine BEST1 variations identifies new mutations and establishes an independent bestrophinopathy model (cmr3).

Zangerl B, Wickström K, Slavik J, Lindauer SJ, Ahonen S, Schelling C, Lohi H, Guziewicz KE, Aguirre GD. Zangerl B, et al. Among authors: lohi h. Mol Vis. 2010 Dec 16;16:2791-804. Mol Vis. 2010. PMID: 21197113 Free PMC article.

7

Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping.

Vaysse A, Ratnakumar A, Derrien T, Axelsson E, Rosengren Pielberg G, Sigurdsson S, Fall T, Seppälä EH, Hansen MS, Lawley CT, Karlsson EK; LUPA Consortium; Bannasch D, Vilà C, Lohi H, Galibert F, Fredholm M, Häggström J, Hedhammar A, André C, Lindblad-Toh K, Hitte C, Webster MT. Vaysse A, et al. Among authors: lohi h. PLoS Genet. 2011 Oct;7(10):e1002316. doi: 10.1371/journal.pgen.1002316. Epub 2011 Oct 13. PLoS Genet. 2011. PMID: 22022279 Free PMC article.

8

A novel GUSB mutation in Brazilian terriers with severe skeletal abnormalities defines the disease as mucopolysaccharidosis VII.

Hytönen MK, Arumilli M, Lappalainen AK, Kallio H, Snellman M, Sainio K, Lohi H. Hytönen MK, et al. Among authors: lohi h. PLoS One. 2012;7(7):e40281. doi: 10.1371/journal.pone.0040281. Epub 2012 Jul 5. PLoS One. 2012. PMID: 22815736 Free PMC article.

9

Behavioral Abnormalities in Lagotto Romagnolo Dogs with a History of Benign Familial Juvenile Epilepsy: A Long-Term Follow-Up Study.

Jokinen TS, Tiira K, Metsähonkala L, Seppälä EH, Hielm-Björkman A, Lohi H, Laitinen-Vapaavuori O. Jokinen TS, et al. Among authors: lohi h. J Vet Intern Med. 2015 Jul-Aug;29(4):1081-7. doi: 10.1111/jvim.12611. Epub 2015 May 6. J Vet Intern Med. 2015. PMID: 25945683 Free PMC article.

10

Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.

Hytönen MK, Arumilli M, Lappalainen AK, Owczarek-Lipska M, Jagannathan V, Hundi S, Salmela E, Venta P, Sarkiala E, Jokinen T, Gorgas D, Kere J, Nieminen P, Drögemüller C, Lohi H. Hytönen MK, et al. Among authors: lohi h. PLoS Genet. 2016 May 17;12(5):e1006037. doi: 10.1371/journal.pgen.1006037. eCollection 2016 May. PLoS Genet. 2016. PMID: 27187611 Free PMC article.

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