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Items: 1 to 50 of 273

1.

APOB-associated cholesterol deficiency in Holstein cattle is not a simple recessive disease.

Häfliger IM, Hofstetter S, Mock T, Stettler MH, Meylan M, Mehinagic K, Stokar-Regenscheit N, Drögemüller C.

Anim Genet. 2019 Jun 18. doi: 10.1111/age.12801. [Epub ahead of print]

PMID:
31215050
2.

Phenotypic Effects of FGF4 Retrogenes on Intervertebral Disc Disease in Dogs.

Batcher K, Dickinson P, Giuffrida M, Sturges B, Vernau K, Knipe M, Rasouliha SH, Drögemüller C, Leeb T, Maciejczyk K, Jenkins CA, Mellersh C, Bannasch D.

Genes (Basel). 2019 Jun 7;10(6). pii: E435. doi: 10.3390/genes10060435.

3.

Identification of a Missense Variant in MFSD12 Involved in Dilution of Phaeomelanin Leading to White or Cream Coat Color in Dogs.

Hédan B, Cadieu E, Botherel N, Dufaure de Citres C, Letko A, Rimbault M, Drögemüller C, Jagannathan V, Derrien T, Schmutz S, Leeb T, André C.

Genes (Basel). 2019 May 21;10(5). pii: E386. doi: 10.3390/genes10050386.

4.

A Missense Variant in SCN8A in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia.

Letko A, Dietschi E, Nieburg M, Jagannathan V, Gurtner C, Oevermann A, Drögemüller C.

Genes (Basel). 2019 May 10;10(5). pii: E362. doi: 10.3390/genes10050362.

5.

Chromosomal imbalance in pigs showing a syndromic form of cleft palate.

Grahofer A, Letko A, Häfliger IM, Jagannathan V, Ducos A, Richard O, Peter V, Nathues H, Drögemüller C.

BMC Genomics. 2019 May 8;20(1):349. doi: 10.1186/s12864-019-5711-4.

6.

Polymelia in a chimeric Simmental calf: nociceptive withdrawal reflex, anaesthetic and analgesic management, anatomic and genetic analysis.

Morath-Huss U, Drögemüller C, Stoffel M, Precht C, Zanolari P, Spadavecchia C.

BMC Vet Res. 2019 Mar 29;15(1):102. doi: 10.1186/s12917-019-1846-4.

7.

Australia and New Zealand Islet and Pancreas Transplant Registry Annual Report 2018-Islet Donations, Islet Isolations, and Islet Transplants.

Webster AC, Hedley JA, Anderson PF, Hawthorne WJ, Radford T, Drogemuller C, Rogers N, Goodman D, Lee MH, Loudovaris T, Kelly PJ.

Transplant Direct. 2019 Jan 7;5(2):e421. doi: 10.1097/TXD.0000000000000851. eCollection 2019 Feb.

8.

Development of a Coaxial 3D Printing Platform for Biofabrication of Implantable Islet-Containing Constructs.

Liu X, Carter SD, Renes MJ, Kim J, Rojas-Canales DM, Penko D, Angus C, Beirne S, Drogemuller CJ, Yue Z, Coates PT, Wallace GG.

Adv Healthc Mater. 2019 Apr;8(7):e1801181. doi: 10.1002/adhm.201801181. Epub 2019 Jan 11.

PMID:
30633852
9.

[Unilateral peromelia of the left pelvic limb in a Brown Swiss calf].

Hofstetter S, Pieńkowska-Schelling A, von Rotz A, Drögemüller C.

Schweiz Arch Tierheilkd. 2019 Jan;161(1):59-64. doi: 10.17236/sat00194. German.

10.

Comprehensive characterization of horse genome variation by whole-genome sequencing of 88 horses.

Jagannathan V, Gerber V, Rieder S, Tetens J, Thaller G, Drögemüller C, Leeb T.

Anim Genet. 2019 Feb;50(1):74-77. doi: 10.1111/age.12753. Epub 2018 Dec 7.

PMID:
30525216
11.

A non-coding regulatory variant in the 5'-region of the MITF gene is associated with white-spotted coat in Brown Swiss cattle.

Hofstetter S, Seefried F, Häfliger IM, Jagannathan V, Leeb T, Drögemüller C.

Anim Genet. 2019 Feb;50(1):27-32. doi: 10.1111/age.12751. Epub 2018 Dec 2.

PMID:
30506810
12.

A COL2A1 de novo variant in a Holstein bulldog calf.

Häfliger IM, Behn H, Freick M, Jagannathan V, Drögemüller C.

Anim Genet. 2019 Feb;50(1):113-114. doi: 10.1111/age.12735. Epub 2018 Oct 31. No abstract available.

PMID:
30378686
13.

Genetic risk for squamous cell carcinoma of the nictitating membrane parallels that of the limbus in Haflinger horses.

Singer-Berk M, Knickelbein KE, Vig S, Liu J, Bentley E, Nunnery C, Reilly C, Dwyer A, Drögemüller C, Unger L, Gerber V, Lassaline M, Bellone RR.

Anim Genet. 2018 Oct;49(5):457-460. doi: 10.1111/age.12695. Epub 2018 Jul 12.

PMID:
29999543
14.

Murine and Non-Human Primate Dendritic Cell Targeting Nanoparticles for in Vivo Generation of Regulatory T-Cells.

Stead SO, Kireta S, McInnes SJP, Kette FD, Sivanathan KN, Kim J, Cueto-Diaz EJ, Cunin F, Durand JO, Drogemuller CJ, Carroll RP, Voelcker NH, Coates PT.

ACS Nano. 2018 Jul 24;12(7):6637-6647. doi: 10.1021/acsnano.8b01625. Epub 2018 Jul 11.

PMID:
29979572
15.

A Missense Mutation in the Vacuolar Protein Sorting 11 (VPS11) Gene Is Associated with Neuroaxonal Dystrophy in Rottweiler Dogs.

Lucot KL, Dickinson PJ, Finno CJ, Mansour TA, Letko A, Minor KM, Mickelson JR, Drögemüller C, Brown CT, Bannasch DL.

G3 (Bethesda). 2018 Jul 31;8(8):2773-2780. doi: 10.1534/g3.118.200376.

16.

Evaluation of HOXC8 in crested Swiss chicken.

Joller S, Ammann P, Flury C, Drögemüller C.

Anim Genet. 2018 Aug;49(4):334-336. doi: 10.1111/age.12674. Epub 2018 May 18.

PMID:
29774580
17.

[Bovine dilated cardiomyopathy: Almost forgotten but still present].

Riedi A, Drögemüller C, Gurtner C, Meylan M.

Schweiz Arch Tierheilkd. 2018 May;160(5):289-293. doi: 10.17236/sat00158. German.

18.

Canine NAPEPLD-associated models of human myelin disorders.

Minor KM, Letko A, Becker D, Drögemüller M, Mandigers PJJ, Bellekom SR, Leegwater PAJ, Stassen QEM, Putschbach K, Fischer A, Flegel T, Matiasek K, Ekenstedt KJ, Furrow E, Patterson EE, Platt SR, Kelly PA, Cassidy JP, Shelton GD, Lucot K, Bannasch DL, Martineau H, Muir CF, Priestnall SL, Henke D, Oevermann A, Jagannathan V, Mickelson JR, Drögemüller C.

Sci Rep. 2018 Apr 11;8(1):5818. doi: 10.1038/s41598-018-23938-7.

19.

[Fanconi-Bickel-Syndrom: a novel genetic disease in Original Braunvieh].

Joller S, Stettler M, Locher I, Dettwiler M, Seefried F, Meylan M, Drögemüller C.

Schweiz Arch Tierheilkd. 2018 Mar;160(3):179-184. doi: 10.17236/sat00152. German.

20.

Crossed beaks in a local Swiss chicken breed.

Joller S, Bertschinger F, Kump E, Spiri A, von Rotz A, Schweizer-Gorgas D, Drögemüller C, Flury C.

BMC Vet Res. 2018 Mar 5;14(1):68. doi: 10.1186/s12917-018-1398-z.

21.

Oxygen-permeable microwell device maintains islet mass and integrity during shipping.

Rojas-Canales DM, Waibel M, Forget A, Penko D, Nitschke J, Harding FJ, Delalat B, Blencowe A, Loudovaris T, Grey ST, Thomas HE, Kay TWH, Drogemuller CJ, Voelcker NH, Coates PT.

Endocr Connect. 2018 Mar;7(3):490-503. doi: 10.1530/EC-17-0349. Epub 2018 Feb 26.

22.

Meta-analysis of genome-wide association studies for cattle stature identifies common genes that regulate body size in mammals.

Bouwman AC, Daetwyler HD, Chamberlain AJ, Ponce CH, Sargolzaei M, Schenkel FS, Sahana G, Govignon-Gion A, Boitard S, Dolezal M, Pausch H, Brøndum RF, Bowman PJ, Thomsen B, Guldbrandtsen B, Lund MS, Servin B, Garrick DJ, Reecy J, Vilkki J, Bagnato A, Wang M, Hoff JL, Schnabel RD, Taylor JF, Vinkhuyzen AAE, Panitz F, Bendixen C, Holm LE, Gredler B, Hozé C, Boussaha M, Sanchez MP, Rocha D, Capitan A, Tribout T, Barbat A, Croiseau P, Drögemüller C, Jagannathan V, Vander Jagt C, Crowley JJ, Bieber A, Purfield DC, Berry DP, Emmerling R, Götz KU, Frischknecht M, Russ I, Sölkner J, Van Tassell CP, Fries R, Stothard P, Veerkamp RF, Boichard D, Goddard ME, Hayes BJ.

Nat Genet. 2018 Mar;50(3):362-367. doi: 10.1038/s41588-018-0056-5. Epub 2018 Feb 19.

PMID:
29459679
23.

Manipulating human dendritic cell phenotype and function with targeted porous silicon nanoparticles.

Stead SO, McInnes SJP, Kireta S, Rose PD, Jesudason S, Rojas-Canales D, Warther D, Cunin F, Durand JO, Drogemuller CJ, Carroll RP, Coates PT, Voelcker NH.

Biomaterials. 2018 Feb;155:92-102. doi: 10.1016/j.biomaterials.2017.11.017. Epub 2017 Nov 20.

PMID:
29175084
24.

Differential distribution of Y-chromosome haplotypes in Swiss and Southern European goat breeds.

Vidal O, Drögemüller C, Obexer-Ruff G, Reber I, Jordana J, Martínez A, Bâlteanu VA, Delgado JV, Eghbalsaied S, Landi V, Goyache F, Traoré A, Pazzola M, Vacca GM, Badaoui B, Pilla F, D'Andrea M, Álvarez I, Capote J, Sharaf A, Pons À, Amills M.

Sci Rep. 2017 Nov 23;7(1):16161. doi: 10.1038/s41598-017-15593-1.

25.

Two brown coat colour-associated TYRP1 variants (bc and bd ) occur in Leonberger dogs.

Letko A, Drögemüller C.

Anim Genet. 2017 Dec;48(6):732-733. doi: 10.1111/age.12612. Epub 2017 Oct 5. No abstract available.

PMID:
28983931
26.

A genome-wide significant association on chromosome 2 for footrot resistance/susceptibility in Swiss White Alpine sheep.

Niggeler A, Tetens J, Stäuble A, Steiner A, Drögemüller C.

Anim Genet. 2017 Dec;48(6):712-715. doi: 10.1111/age.12614. Epub 2017 Oct 5.

PMID:
28983925
27.

Rapid Discovery of De Novo Deleterious Mutations in Cattle Enhances the Value of Livestock as Model Species.

Bourneuf E, Otz P, Pausch H, Jagannathan V, Michot P, Grohs C, Piton G, Ammermüller S, Deloche MC, Fritz S, Leclerc H, Péchoux C, Boukadiri A, Hozé C, Saintilan R, Créchet F, Mosca M, Segelke D, Guillaume F, Bouet S, Baur A, Vasilescu A, Genestout L, Thomas A, Allais-Bonnet A, Rocha D, Colle MA, Klopp C, Esquerré D, Wurmser C, Flisikowski K, Schwarzenbacher H, Burgstaller J, Brügmann M, Dietschi E, Rudolph N, Freick M, Barbey S, Fayolle G, Danchin-Burge C, Schibler L, Bed'Hom B, Hayes BJ, Daetwyler HD, Fries R, Boichard D, Pin D, Drögemüller C, Capitan A.

Sci Rep. 2017 Sep 13;7(1):11466. doi: 10.1038/s41598-017-11523-3.

28.

Liver transcriptome analysis reveals important factors involved in the metabolic adaptation of the transition cow.

Ha NT, Drögemüller C, Reimer C, Schmitz-Hsu F, Bruckmaier RM, Simianer H, Gross JJ.

J Dairy Sci. 2017 Nov;100(11):9311-9323. doi: 10.3168/jds.2016-12454. Epub 2017 Aug 31.

29.

Dermatosparaxis in White Dorper sheep: confirmation of a causative nonsense mutation in ADAMTS2.

Joller S, Berenguer Veiga I, Drögemüller C.

Anim Genet. 2017 Dec;48(6):729-730. doi: 10.1111/age.12591. Epub 2017 Aug 30. No abstract available.

PMID:
28856769
30.

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs.

Becker D, Minor KM, Letko A, Ekenstedt KJ, Jagannathan V, Leeb T, Shelton GD, Mickelson JR, Drögemüller C.

BMC Genomics. 2017 Aug 25;18(1):662. doi: 10.1186/s12864-017-4081-z.

31.

A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle.

Agerholm JS, McEvoy FJ, Heegaard S, Charlier C, Jagannathan V, Drögemüller C.

BMC Genet. 2017 Aug 2;18(1):74. doi: 10.1186/s12863-017-0541-3.

32.

A de novo germline mutation of DLX3 in a Brown Swiss calf with tricho-dento-osseus-like syndrome.

Hofstetter S, Welle M, Gorgas D, Balmer P, Roosje P, Mock T, Meylan M, Jagannathan V, Drögemüller C.

Vet Dermatol. 2017 Dec;28(6):616-e150. doi: 10.1111/vde.12462. Epub 2017 Jul 2.

PMID:
28670783
33.

A structural variant in the 5'-flanking region of the TWIST2 gene affects melanocyte development in belted cattle.

Awasthi Mishra N, Drögemüller C, Jagannathan V, Keller I, Wüthrich D, Bruggmann R, Beck J, Schütz E, Brenig B, Demmel S, Moser S, Signer-Hasler H, Pieńkowska-Schelling A, Schelling C, Sande M, Rongen R, Rieder S, Kelsh RN, Mercader N, Leeb T.

PLoS One. 2017 Jun 28;12(6):e0180170. doi: 10.1371/journal.pone.0180170. eCollection 2017.

34.

A missense mutation in damage-specific DNA binding protein 2 is a genetic risk factor for limbal squamous cell carcinoma in horses.

Bellone RR, Liu J, Petersen JL, Mack M, Singer-Berk M, Drögemüller C, Malvick J, Wallner B, Brem G, Penedo MC, Lassaline M.

Int J Cancer. 2017 Jul 15;141(2):342-353. doi: 10.1002/ijc.30744. Epub 2017 May 8.

35.

First Report of Successful Total Pancreatectomy and Islet Autotransplant in Australia.

Geyer MC, Coates PT, Khurana S, Chen JW, Kay TW, Balamurugan AN, Couper JJ, Radford T, Drogemuller CJ, Loudovaris T, Pathi R, Wilks MJ, Couper RT.

Pancreas. 2017 Mar;46(3):e18-e20. doi: 10.1097/MPA.0000000000000769. No abstract available.

PMID:
28187110
36.

Local Sphingosine Kinase 1 Activity Improves Islet Transplantation.

Rojas-Canales D, Penko D, Myo Min KK, Parham KA, Peiris H, Haberberger RV, Pitson SM, Drogemuller C, Keating DJ, Grey ST, Coates PT, Bonder CS, Jessup CF.

Diabetes. 2017 May;66(5):1301-1311. doi: 10.2337/db16-0837. Epub 2017 Feb 7.

37.

Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog.

Hirz M, Drögemüller M, Schänzer A, Jagannathan V, Dietschi E, Goebel HH, Hecht W, Laubner S, Schmidt MJ, Steffen F, Hilbe M, Köhler K, Drögemüller C, Herden C.

Mol Genet Metab. 2017 Mar;120(3):269-277. doi: 10.1016/j.ymgme.2016.12.007. Epub 2016 Dec 19.

PMID:
28024876
38.

A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle.

Murgiano L, Jagannathan V, Piffer C, Diez-Prieto I, Bolcato M, Gentile A, Drögemüller C.

BMC Vet Res. 2016 Dec 5;12(1):276.

39.

A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle.

Pausch H, Ammermüller S, Wurmser C, Hamann H, Tetens J, Drögemüller C, Fries R.

BMC Genet. 2016 Dec 1;17(1):149.

40.

Genetic diversity analyses reveal first insights into breed-specific selection signatures within Swiss goat breeds.

Burren A, Neuditschko M, Signer-Hasler H, Frischknecht M, Reber I, Menzi F, Drögemüller C, Flury C.

Anim Genet. 2016 Dec;47(6):727-739. doi: 10.1111/age.12476. Epub 2016 Jul 20.

PMID:
27436146
41.

A Combinatorial Protein Microarray for Probing Materials Interaction with Pancreatic Islet Cell Populations.

Delalat B, Rojas-Canales DM, Rasi Ghaemi S, Waibel M, Harding FJ, Penko D, Drogemuller CJ, Loudovaris T, Coates PT, Voelcker NH.

Microarrays (Basel). 2016 Aug 10;5(3). pii: E21. doi: 10.3390/microarrays5030021.

42.

A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype.

Waluk DP, Zur G, Kaufmann R, Welle MM, Jagannathan V, Drögemüller C, Müller EJ, Leeb T, Galichet A.

G3 (Bethesda). 2016 Sep 8;6(9):2949-54. doi: 10.1534/g3.116.033225.

43.

Full-genome based molecular characterization of encephalitis-associated bovine astroviruses.

Bouzalas IG, Wüthrich D, Selimovic-Hamza S, Drögemüller C, Bruggmann R, Seuberlich T.

Infect Genet Evol. 2016 Oct;44:162-168. doi: 10.1016/j.meegid.2016.06.052. Epub 2016 Jul 1.

44.

A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle.

Agerholm JS, McEvoy FJ, Menzi F, Jagannathan V, Drögemüller C.

BMC Genomics. 2016 Jun 30;17:479. doi: 10.1186/s12864-016-2832-x.

45.

Genomic amplification of the caprine EDNRA locus might lead to a dose dependent loss of pigmentation.

Menzi F, Keller I, Reber I, Beck J, Brenig B, Schütz E, Leeb T, Drögemüller C.

Sci Rep. 2016 Jun 22;6:28438. doi: 10.1038/srep28438.

46.

Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1.

Agerholm JS, Menzi F, McEvoy FJ, Jagannathan V, Drögemüller C.

BMC Vet Res. 2016 Jun 13;12:100. doi: 10.1186/s12917-016-0739-z.

47.

Clinicopathological Phenotype of Autosomal Recessive Cholesterol Deficiency in Holstein Cattle.

Mock T, Mehinagic K, Menzi F, Studer E, Oevermann A, Stoffel MH, Drögemüller C, Meylan M, Regenscheit N.

J Vet Intern Med. 2016 Jul;30(4):1369-75. doi: 10.1111/jvim.13976. Epub 2016 Jun 8.

48.

Pulmonary hypoplasia and anasarca syndrome in Cika cattle.

Švara T, Cociancich V, Šest K, Gombač M, Paller T, Starič J, Drögemüller C.

Acta Vet Scand. 2016 Jun 6;58(1):36. doi: 10.1186/s13028-016-0220-9.

49.

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.

PLoS Genet. 2016 May 17;12(5):e1006037. doi: 10.1371/journal.pgen.1006037. eCollection 2016 May.

50.

[Inherited thrombopathia in Simmental cattle].

Aebi M, Wiedemar N, Drögemüller C, Zanolari R.

Schweiz Arch Tierheilkd. 2016 Feb;158(2):102-8. German.

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