Publikationen

Publikationen AG Hashemolhosseini

2021

Durmus H., Mertoğlu E., Sticht H., Ceylaner S., Kulaksızoğlu IB., Hashemolhosseini S., Uçar EÖ., Parman Y.:
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP sydrome) caused by a novel mutation in ADPRHL2 (AHR3)
In: Neurological Sciences (2021)
ISSN: 1590-1874
DOI: 10.1007/s10072-021-05100-w

2020

Durmus H., Sticht H., Ceylaner S., Hashemolhosseini S., Deymeer F.:
Rare slow channel congenital myasthenic syndromes without repetitive compound muscle action potential and dramatic response to low dose fluoxetine
In: Acta Neurologica Belgica (2020)
ISSN: 0300-9009
DOI: 10.1007/s13760-020-01505-0
Durmus H., Sticht H., Ceylaner S., Hashemolhosseini S., Parmn Y.:
EPISODIC PSYCHOSIS, ATAXIA, MOTOR NEUROPATHY CAUSED BY A NOVEL MUTATION IN ADPRHL2
Annual Meeting of the American-Academy-of-Neurology (Toronto, CANADA, 25. April 2020 - 1. Mai 2020)
In: NEUROLOGY, PHILADELPHIA: 2020
Eiber N., Fröb F., Schowalter M., Thiel C., Clemen CS., Schröder R., Hashemolhosseini S.:
Lack of Desmin in Mice Causes Structural and Functional Disorders of Neuromuscular Junctions
In: Frontiers in Molecular Neuroscience 13 (2020)
ISSN: 1662-5099
DOI: 10.3389/fnmol.2020.567084
Hashemolhosseini S.:
The role of protein kinase CK2 in skeletal muscle: Myogenesis, neuromuscular junctions, and rhabdomyosarcoma
In: Neuroscience Letters 729 (2020), Art.Nr.: 135001
ISSN: 0304-3940
DOI: 10.1016/j.neulet.2020.135001
Zhang Y., Otto P., Qin L., Eiber N., Hashemolhosseini S., Kröger S., Brinkmeier H.:
Methocarbamol blocks muscular Nav1.4 channels and decreases isometric force of mouse muscles
In: Muscle & Nerve (2020)
ISSN: 0148-639X
DOI: 10.1002/mus.27087

2019

Eiber N., Rehman M., Kravic B., Rudolf R., Sandri M., Hashemolhosseini S.:
Loss of Protein Kinase Csnk2b/CK2 beta at Neuromuscular Junctions Affects Morphology and Dynamics of Aggregated Nicotinic Acetylcholine Receptors, Neuromuscular Transmission, and Synaptic Gene Expression
In: Cells 8 (2019)
ISSN: 2073-4409
DOI: 10.3390/cells8080940

2018

Cescon M., Gregorio I., Eiber N., Borgia D., Fusto A., Sabatelli P., Scorzeto M., Megighian A., Pegoraro E., Hashemolhosseini S., Bonaldo P.:
Collagen VI is required for the structural and functional integrity of the neuromuscular junction
In: Acta Neuropathologica 136 (2018), S. 483-499
ISSN: 0001-6322
DOI: 10.1007/s00401-018-1860-9

2017

Dorninger F., Herbst R., Kravic B., Camurdanoglu BZ., Macinkovic I., Zeitler G., Forss-Petter S., Strack S., Khan MM., Waterham HR., Rudolf R., Hashemolhosseini S., Berger J.:
Reduced muscle strength in ether lipid-deficient mice is accompanied by altered development and function of the neuromuscular junction
In: Journal of Neurochemistry 143 (2017), S. 569-583
ISSN: 0022-3042
DOI: 10.1111/jnc.14082
Eiber N., Simeone L., Hashemolhosseini S.:
Ablation of Protein Kinase CK2β in Skeletal Muscle Fibers Interferes with Their Oxidative Capacity
In: Pharmaceuticals 10 (2017)
ISSN: 1424-8247
DOI: 10.3390/ph10010013
Giacomazzi G., Holvoet B., Trenson S., Caluwe E., Kravic B., Grosemans H., Cortes-Calabuig A., Deroose CM., Huylebroeck D., Hashemolhosseini S., Janssens S., Mcnally E., Quattrocelli M., Sampaolesi M.:
MicroRNAs promote skeletal muscle differentiation of mesodermal iPSC-derived progenitors
In: Nature Communications 8 (2017)
ISSN: 2041-1723
DOI: 10.1038/s41467-017-01359-w
Kravic B., Harbauer AB., Romanello V., Simeone L., Vögtle FN., Kaiser T., Straubinger M., Huraskin D., Böttcher M., Cerqua C., Martin ED., Poveda-Huertes D., Buttgereit A., Rabalski AJ., Heuss D., Rudolf R., Friedrich O., Litchfield D., Marber M., Salviati L., Mougiakakos D., Neuhuber W., Sandri M., Meisinger C., Hashemolhosseini S.:
In mammalian skeletal muscle, phosphorylation of TOMM22 by protein kinase CSNK2/CK2 controls mitophagy
In: Autophagy (2017), S. 1-65
ISSN: 1554-8627
DOI: 10.1080/15548627.2017.1403716

2016

Durmus H., Ayhan O., Cirak S., Deymeer F., Parman Y., Franke A., Eiber N., Chevessier F., Schlötzer-Schrehardt U., Clemen CS., Hashemolhosseini S., Schröder R., Hemmrich-Stanisak G., Tolun A., Serdaroglu-Oflazer P.:
Neuromuscular endplate pathology in recessive desminopathies: Lessons from man and mice
In: Neurology 87 (2016), S. 799-805
ISSN: 0028-3878
DOI: 10.1212/WNL.0000000000003004
Huraskin D., Eiber N., Reichel M., Zidek LM., Kravic B., Bernkopf D., von Maltzahn J., Behrens J., Hashemolhosseini S.:
Wnt/?-catenin signaling via Axin2 is required for myogenesis and, together with YAP/Taz and Tead1, active in IIa/IIx muscle fibers
In: Development 143 (2016), S. 3128-42
ISSN: 1477-9129
DOI: 10.1242/dev.139907
Kravic B., Huraskin D., Frick A., Jung J., Redai V., Palmisano R., Marchetto S., Borg JP., Mei L., Hashemolhosseini S.:
LAP proteins are localized at the post-synaptic membrane of neuromuscular junctions and appear to modulate synaptic morphology and transmission
In: Journal of Neurochemistry 139 (2016), S. 381-395
ISSN: 0022-3042
DOI: 10.1111/jnc.13710
Rudolf R., Khan MM., Wild F., Hashemolhosseini S.:
The impact of autophagy on peripheral synapses in health and disease
In: Frontiers in Bioscience 21 (2016), S. 1474-87
ISSN: 1093-9946
DOI: 10.2741/4467

2015

Herrmann D., Straubinger M., Hashemolhosseini S.:
Protein kinase CK2 interacts at the neuromuscular synapse with Rapsyn, Rac1, 14-3-3?, and Dok-7 proteins and phosphorylates the latter two
In: Journal of Biological Chemistry 290 (2015), S. 22370-84
ISSN: 0021-9258
DOI: 10.1074/jbc.M115.647610

2006

Cheusova T., Khan MA., Enz R., Hashemolhosseini S.:
Identification of developmentally regulated expression of MuSK in astrocytes of the rodent retina.
In: Journal of Neurochemistry (2006), S. 450-457
ISSN: 0022-3042
DOI: 10.1111/j.1471-4159.2006.04086.x
Cheusova T., Khan MA., Schubert S., Gavin AC., Buchou T., Jacob G., Sticht H., Allende J., Boldyreff B., Brenner HR., Hashemolhosseini S.:
Casein kinase 2-dependent serine phosphorylation of MuSK regulates acetylcholine receptor aggregation at the neuromuscular junction.
In: Genes & Development (2006), S. 1800-1816
ISSN: 0890-9369
DOI: 10.1101/gad.375206

2005

Thomee C., Schubert S.W., Parma J., Le P.Q., Hashemolhosseini Said, Wegner Michael, Abramowicz M.J.:
GCMB mutation in familial isolated hypo-parathyroidism with residual secretion of parathyroid hormone.
In: Journal of Clinical Endocrinology and Metabolism (2005), S. 2487-2492
ISSN: 0021-972X

2004

Hashemolhosseini Said, Schmidt K., Kilian K., Rodriguez E., Wegner Michael:
Conservation and variation of structure and function in a newly identified GCM homolog from chicken
In: Journal of Molecular Biology (2004), S. 441-451
ISSN: 0022-2836
DOI: 10.1016/j.jmb.2003.12.029
Wegner M., Hashemolhosseini S.:
Impacts of a new trancription factor family: Mammalian GCM proteins in health and disease.
In: The Journal of Cell Biology (2004), S. 765-768
ISSN: 0021-9525

2003

Cohen Serge X., Moulin Martine, Hashemolhosseini Said, Kilian Karin, Wegner Michael, Müller Christoph W.:
Structure of the GCM domain-DNA complex: a DNA-binding domain with a novel fold and mode of target site recognition
In: EMBO Journal 22 (2003), S. 1835-45
ISSN: 0261-4189
DOI: 10.1093/emboj/cdg182

2002

Hashemolhosseini S., Hadjihannas M., Haase C., Amann KU., Wegner M.:
Restricted expression of mGCMa in kidney ind thymus
In: Mechanisms of Development (2002), S. in press
ISSN: 0925-4773
Hashemolhosseini Said, Hadjihannas Michel, Stolt Claus, Haas Christian, Amann Kerstin U., Wegner Michael:
Restricted expression of mouse GCMa/Gcm1 in kidney and thymus
In: Mechanisms of Development 118 (2002), S. 175-178
ISSN: 0925-4773
DOI: 10.1016/S0925-4773(02)00239-3

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Publikationen AG Hashemolhosseini

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