Analysis of Polycerate Mutants Reveals the Evolutionary Co-option of HOXD1 for Horn Patterning in Bovidae

Autor: Daniele Bigi, Fiona Menzi, Slim Ben Jemaa, Marie-Christine Deloche, Aurélien Capitan, Johannes A. Lenstra, Marina Naval-Sanchez, Ivica Medugorac, Nathalie Hirter, Gwenola Tosser-Klopp, Diane Esquerre, Coralie M. Reich, Julia M. Paris, Rose-Marie Arbogast, Amandine Blin, Abdelhak Boukadiri, Aurélie Hintermann, Julie Rivière, Denis Duboule, Raphaël Cornette, Cécile Donnadieu, Marie-Dominique Wandhammer, Gjoko Bunevski, Louisa Gidney, Michael Stache, Isabelle Palhiere, Renate Schafberg, James Kijas, Claude Guintard, Joséphine Lesur, Jozsef Zakany, Rachel Rupp, Noelle E. Cockett, John Hedges, Ashleigh Haruda, Philippe Bardou, Olivier Putelat, Tracy Hadfield, Alain Pinton, Ockert Greyvenstein, Aurélie Allais-Bonnet, Este Van Marle-Koster, Eric Pailhoux, Coralie Danchin-Burge, David G. Riley, Cécile Grohs, Benjamin J. Hayes, Cord Drögemüller

Publikováno v: Molecular Biology and Evolution
Molecular Biology and Evolution, Oxford University Press (OUP), 2021, ⟨10.1093/molbev/msab021⟩
Allais-Bonnet, Aurélie; Hintermann, Aurélie; Deloche, Marie-Christine; Cornette, Raphaël; Bardou, Philippe; Naval-Sanchez, Marina; Pinton, Alain; Haruda, Ashleigh; Grohs, Cécile; Zakany, Jozsef; Bigi, Daniele; Medugorac, Ivica; Putelat, Olivier; Greyvenstein, Ockert; Hadfield, Tracy; Jemaa, Slim Ben; Bunevski, Gjoko; Menzi, Fiona; Hirter, Nathalie; Paris, Julia M; ... (2021). Analysis of Polycerate Mutants Reveals the Evolutionary Co-option of HOXD1 for Horn Patterning in Bovidae. Molecular Biology and Evolution, 38(6), pp. 2260-2272. Oxford University Press 10.1093/molbev/msab021
Molecular Biology and Evolution, 2021, ⟨10.1093/molbev/msab021⟩
Molecular Biology and Evolution, 38(6), 2260. Oxford University Press

In the course of evolution, pecorans (i.e., higher ruminants) developed a remarkable diversity of osseous cranial appendages, collectively referred to as “headgear,” which likely share the same origin and genetic basis. However, the nature and fu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e81f9ba5bd3ae8e59d2ce96dcb31adc
https://hal.archives-ouvertes.fr/hal-03164832/file/msab021.pdf

Clinicopathological Phenotype of Autosomal Recessive Cholesterol Deficiency in Holstein Cattle

Autor: Thomas Mock, Eveline Studer, Cord Drögemüller, Michael Hubert Stoffel, Nadine Regenscheit, Anna Oevermann, Mireille Meylan, Kemal Mehinagic, Fiona Menzi

Publikováno v: Journal of Veterinary Internal Medicine
Mock, Thomas; Mehinagic, Kemal; Menzi, Fiona; Studer, Eveline; Oevermann, Anna; Stoffel, Michael Hubert; Drögemüller, Cord; Meylan, Mireille; Regenscheit, Nadine (2016). Clinicopathological Phenotype of Autosomal Recessive Cholesterol Deficiency in Holstein Cattle. Journal of veterinary internal medicine, 30(4), pp. 1369-1375. Wiley-Blackwell 10.1111/jvim.13976

BACKGROUND Cholesterol deficiency (CD), a newly identified autosomal recessive genetic defect in Holstein cattle, is associated with clinical signs of diarrhea, failure to thrive, and hypocholesterolemia. HYPOTHESIS/OBJECTIVES The objective is to des

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f664cdbe2c56346dbfb0f4b703fb3e0b

A transposable element insertion in APOB causes cholesterol deficiency in Holstein cattle

Autor: V. Jagannathan, N. Besuchet‐Schmutz, Sonja Hofstetter, Nadine Regenscheit, Fiona Menzi, Thomas Mock, Kemal Mehinagic, F. Schmitz-Hsu, Mireille Meylan, M. Fragnière, Andreas Raemy, Cord Drögemüller, Eveline Studer

Publikováno v: Menzi, Fiona; Besuchet Schmutz, Nathalie; Fragnière, Muriel; Hofstetter, S; Jagannathan, Vidhya; Mock, Thomas; Raemy, Andreas; Studer, Eveline; Mehinagic, Kemal; Regenscheit, Nadine; Meylan, Mireille; Schmitz-Hsu, F; Drögemüller, Cord (2016). A transposable element insertion in APOB causes cholesterol deficiency in Holstein cattle. Animal genetics, 47(2), pp. 253-257. Blackwell 10.1111/age.12410
Animal Genetics

Summary Cholesterol deficiency, a new autosomal recessive inherited genetic defect in Holstein cattle, has been recently reported to have an influence on the rearing success of calves. The affected animals show unresponsive diarrhea accompanied by hy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ee21bf28cd6b597497c89a41b0fdfbd
https://doi.org/10.1111/age.12410

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

Autor: Fiona Menzi, Fintan J. McEvoy, Vidhya Jagannathan, Cord Drögemüller, Jørgen S. Agerholm

Publikováno v: BMC Veterinary Research
Agerholm, J S, Menzi, F, McEvoy, F, Jagannathan, V & Drögemüller, C 2016, ' Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1 ', BMC Veterinary Research, vol. 12, 100 . https://doi.org/10.1186/s12917-016-0739-z
Agerholm, Jørgen S.; Menzi, Fiona; McEvoy, Fintan J.; Jagannathan, Vidhya; Drögemüller, Cord (2016). Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1. BMC veterinary research, 12(1), p. 100. BioMed Central 10.1186/s12917-016-0739-z

Background Lethal chondrodysplasia (bulldog syndrome) is a well-known congenital syndrome in cattle and occurs sporadically in many breeds. In 2015, it was noticed that about 12 % of the offspring of the phenotypically normal Danish Holstein sire VH

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A breeding experiment confirms the dominant mode of inheritance of the brown coat colour associated with the (496) Asp TYRP1 allele in goats

Autor: Fiona Menzi, Cord Drögemüller, Joëlle Dietrich, Tosso Leeb, P. Ammann

Publikováno v: Animal Genetics

n.a. (Brief Note).

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db6b406797c04cdb29995cd343d1b3e2