Advantages of statin usage in preventing fractures for men over 50 in the United States: National Health and Nutrition Examination Survey.

Autor: Sun, Xiaona^1,2 (AUTHOR), Liu, Xiaoxiao^2,3 (AUTHOR), Wang, Chenyi⁴ (AUTHOR), Luo, Yushuang^1,2 (AUTHOR), Li, Xinyi^1,2 (AUTHOR), Yan, Lijuan⁴ (AUTHOR), Wang, Yaling⁵ (AUTHOR) 930706229@qq.com, Wang, Kaifa¹ (AUTHOR) kfwang72@163.com, Li, Qiang² (AUTHOR) liqianglife@126.com

Publikováno v: PLoS ONE. 11/25/2024, Vol. 19 Issue 11, p1-17. 17p.

Comparison of Mini-FLOTAC, Flukefinder^® and sedimentation techniques for detection and quantification of Fasciola hepatica and Calicophoron daubneyi eggs using spiked and naturally infected bovine faecal samples.

Autor: Bosco, Antonio¹ (AUTHOR), Ciuca, Lavinia¹ (AUTHOR), Maurelli, Maria Paola¹ (AUTHOR) mariapaola.maurelli@unina.it, Vitiello, Paola¹ (AUTHOR), Cringoli, Giuseppe¹ (AUTHOR), Prada, Joaquin M.² (AUTHOR), Rinaldi, Laura¹ (AUTHOR)

Publikováno v: Parasites & Vectors. 8/24/2023, Vol. 16 Issue 1, p1-9. 9p.

Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity

Autor: Da, Collier, Timothy Barrett, Curtis D, Macleod A, Mj, Arranz, Ja, Maassen, Bundey S

Publikováno v: Europe PubMed Central

Wolfram syndrome (DIDMOAD syndrome; MIM 222300) is an autosomal recessive neurodegenerative disorder characterized by juvenile-onset diabetes mellitus and bilateral optic atrophy. Previous linkage analysis of multiply affected families indicated that

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::52d5e8ce8f2fa8f920f3be0b6df5ce1e
http://europepmc.org/abstract/med/8808601

Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach.

Autor: Liautard-Haag, C.¹ (AUTHOR), Durif, G.² (AUTHOR), VanGoethem, C.^1,3 (AUTHOR), Baux, D.^1,4 (AUTHOR), Louis, A.¹ (AUTHOR), Cayrefourcq, L.⁵ (AUTHOR), Lamairia, M.¹ (AUTHOR), Willems, M.⁶ (AUTHOR), Zordan, C.⁷ (AUTHOR), Dorian, V.⁷ (AUTHOR), Rooryck, C.⁷ (AUTHOR), Goizet, C.⁷ (AUTHOR), Chaussenot, A.⁸ (AUTHOR), Monteil, L.⁹ (AUTHOR), Calvas, P.⁹ (AUTHOR), Miry, C.¹⁰ (AUTHOR), Favre, R.¹⁰ (AUTHOR), Le Boette, E.¹¹ (AUTHOR), Fradin, M.¹¹ (AUTHOR), Roux, A. F.^1,4 (AUTHOR)

Publikováno v: Scientific Reports. 7/6/2022, Vol. 12 Issue 1, p1-9. 9p.

Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine.

Autor: Arranz, M.J., Munro, J., Owen, M.J., Spurlock, G., Sham, P.C., Zhao, J., Kirov, G., Collier, D.A., Kerwin, R.W.

Publikováno v: Molecular Psychiatry. 1998, Vol. 3 Issue 1, p61. 6p.