Sacher M - Search Results

1

Munot P, McCrea N, Torelli S, Manzur A, Sewry C, Chambers D, Feng L, Ala P, Zaharieva I, Ragge N, Roper H, Marton T, Cox P, Milev MP, Liang WC, Maruyama S, Nishino I, Sacher M, Phadke R, Muntoni F. Munot P, et al. Among authors: sacher m. Neuropathol Appl Neurobiol. 2022 Feb;48(2):e12771. doi: 10.1111/nan.12771. Epub 2021 Nov 11. Neuropathol Appl Neurobiol. 2022. PMID: 34648194

2

TRAMM/TrappC12 plays a role in chromosome congression, kinetochore stability, and CENP-E recruitment.

Milev MP, Hasaj B, Saint-Dic D, Snounou S, Zhao Q, Sacher M. Milev MP, et al. Among authors: sacher m. J Cell Biol. 2015 Apr 27;209(2):221-34. doi: 10.1083/jcb.201501090. J Cell Biol. 2015. PMID: 25918224 Free PMC article.

3

Mitotic transformation of TRAMM/TrappC12.

Milev MP, Sacher M. Milev MP, et al. Among authors: sacher m. Oncotarget. 2015 Jul 20;6(20):17853-4. doi: 10.18632/oncotarget.4843. Oncotarget. 2015. PMID: 26257002 Free PMC article. No abstract available.

4

Congenital muscular dystrophy with fatty liver and infantile-onset cataract caused by TRAPPC11 mutations: broadening of the phenotype.

Liang WC, Zhu W, Mitsuhashi S, Noguchi S, Sacher M, Ogawa M, Shih HH, Jong YJ, Nishino I. Liang WC, et al. Among authors: sacher m. Skelet Muscle. 2015 Aug 28;5:29. doi: 10.1186/s13395-015-0056-4. eCollection 2015. Skelet Muscle. 2015. PMID: 26322222 Free PMC article.

5

trappc11 is required for protein glycosylation in zebrafish and humans.

DeRossi C, Vacaru A, Rafiq R, Cinaroglu A, Imrie D, Nayar S, Baryshnikova A, Milev MP, Stanga D, Kadakia D, Gao N, Chu J, Freeze HH, Lehrman MA, Sacher M, Sadler KC. DeRossi C, et al. Among authors: sacher m. Mol Biol Cell. 2016 Apr 15;27(8):1220-34. doi: 10.1091/mbc.E15-08-0557. Epub 2016 Feb 24. Mol Biol Cell. 2016. PMID: 26912795 Free PMC article.

6

The TRAPP Subunit Trs130p Interacts with the GAP Gyp6p to Mediate Ypt6p Dynamics at the Late Golgi.

Brunet S, Saint-Dic D, Milev MP, Nilsson T, Sacher M. Brunet S, et al. Among authors: sacher m. Front Cell Dev Biol. 2016 May 24;4:48. doi: 10.3389/fcell.2016.00048. eCollection 2016. Front Cell Dev Biol. 2016. PMID: 27252941 Free PMC article.

7

TRAMM, a new player in CENP-E biology.

Milev MP, Sacher M. Milev MP, et al. Among authors: sacher m. Mol Cell Oncol. 2015 Jun 10;3(1):e1057314. doi: 10.1080/23723556.2015.1057314. eCollection 2016 Jan. Mol Cell Oncol. 2015. PMID: 27308570 Free PMC article.

8

A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima.

Koehler K, Milev MP, Prematilake K, Reschke F, Kutzner S, Jühlen R, Landgraf D, Utine E, Hazan F, Diniz G, Schuelke M, Huebner A, Sacher M. Koehler K, et al. Among authors: sacher m. J Med Genet. 2017 Mar;54(3):176-185. doi: 10.1136/jmedgenet-2016-104108. Epub 2016 Oct 5. J Med Genet. 2017. PMID: 27707803

9

Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction.

Milev MP, Grout ME, Saint-Dic D, Cheng YH, Glass IA, Hale CJ, Hanna DS, Dorschner MO, Prematilake K, Shaag A, Elpeleg O, Sacher M, Doherty D, Edvardson S. Milev MP, et al. Among authors: sacher m. Am J Hum Genet. 2017 Aug 3;101(2):291-299. doi: 10.1016/j.ajhg.2017.07.006. Am J Hum Genet. 2017. PMID: 28777934 Free PMC article.

10

TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of α-dystroglycan and muscular dystrophy.

Larson AA, Baker PR 2nd, Milev MP, Press CA, Sokol RJ, Cox MO, Lekostaj JK, Stence AA, Bossler AD, Mueller JM, Prematilake K, Tadjo TF, Williams CA, Sacher M, Moore SA. Larson AA, et al. Among authors: sacher m. Skelet Muscle. 2018 May 31;8(1):17. doi: 10.1186/s13395-018-0163-0. Skelet Muscle. 2018. PMID: 29855340 Free PMC article.

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