Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 254

1.

Redox Proteomes in Human Physiology and Disease Mechanisms.

Mannaa A, Hanisch FG.

J Proteome Res. 2019 Nov 8. doi: 10.1021/acs.jproteome.9b00586. [Epub ahead of print]

PMID:
31647248
2.
3.

[Cobalamin deficiency in dogs and cats].

Hanisch F, Toresson L, Spillmann T.

Tierarztl Prax Ausg K Kleintiere Heimtiere. 2018 Oct;46(5):309-314. doi: 10.15654/TPK-180458. Epub 2018 Dec 12. Review. German.

PMID:
30541171
4.

Functional Roles of O-Glycosylation.

Breloy I, Hanisch FG.

Molecules. 2018 Nov 23;23(12). pii: E3063. doi: 10.3390/molecules23123063.

5.

Diagnosis of feline pancreatitis with SNAP fPL and Spec fPL.

Schnauß F, Hanisch F, Burgener IA.

J Feline Med Surg. 2019 Aug;21(8):700-707. doi: 10.1177/1098612X18796624. Epub 2018 Sep 5.

6.

Avidity of α-fucose on human milk oligosaccharides and blood group-unrelated oligo/polyfucoses is essential for potent norovirus-binding targets.

Hanisch FG, Hansman GS, Morozov V, Kunz C, Schroten H.

J Biol Chem. 2018 Jul 27;293(30):11955-11965. doi: 10.1074/jbc.RA117.001369. Epub 2018 Jun 1.

7.

The Double Face of Mucin-Type O-Glycans in Lectin-Mediated Infection and Immunity.

Morozov V, Borkowski J, Hanisch FG.

Molecules. 2018 May 11;23(5). pii: E1151. doi: 10.3390/molecules23051151. Review.

8.

Single molecule real time sequencing in ADTKD-MUC1 allows complete assembly of the VNTR and exact positioning of causative mutations.

Wenzel A, Altmueller J, Ekici AB, Popp B, Stueber K, Thiele H, Pannes A, Staubach S, Salido E, Nuernberg P, Reinhardt R, Reis A, Rump P, Hanisch FG, Wolf MTF, Wiesener M, Huettel B, Beck BB.

Sci Rep. 2018 Mar 8;8(1):4170. doi: 10.1038/s41598-018-22428-0.

9.

The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy.

Rosenbohm A, Hirsch S, Volk AE, Grehl T, Grosskreutz J, Hanisch F, Herrmann A, Kollewe K, Kress W, Meyer T, Petri S, Prudlo J, Wessig C, Müller HP, Dreyhaupt J, Weishaupt J, Kubisch C, Kassubek J, Weydt P, Ludolph AC.

J Neurol. 2018 May;265(5):1026-1036. doi: 10.1007/s00415-018-8790-2. Epub 2018 Feb 20.

PMID:
29464380
10.

Autosomal Tubulointerstitial Kidney Disease-MUC1 Type: Differential Proteomics Suggests that Mutated MUC1 (insC) Affects Vesicular Transport in Renal Epithelial Cells.

Staubach S, Wenzel A, Beck BB, Rinschen MM, Müller S, Hanisch FG.

Proteomics. 2018 Apr;18(7):e1700456. doi: 10.1002/pmic.201700456. Epub 2018 Mar 13.

PMID:
29436780
11.

Human Milk Oligosaccharides as Promising Antivirals.

Morozov V, Hansman G, Hanisch FG, Schroten H, Kunz C.

Mol Nutr Food Res. 2018 Mar;62(6):e1700679. doi: 10.1002/mnfr.201700679. Epub 2018 Mar 1. Review.

PMID:
29336526
12.

Classical Galactosemia: Insight into Molecular Pathomechanisms by Differential Membrane Proteomics of Fibroblasts under Galactose Stress.

Staubach S, Müller S, Pekmez M, Hanisch FG.

J Proteome Res. 2017 Feb 3;16(2):516-527. doi: 10.1021/acs.jproteome.6b00658. Epub 2017 Jan 24.

PMID:
28075131
13.

The concept and diagnostic criteria of primary lateral sclerosis.

Wais V, Rosenbohm A, Petri S, Kollewe K, Hermann A, Storch A, Hanisch F, Zierz S, Nagel G, Kassubek J, Weydt P, Brettschneider J, Weishaupt JH, Ludolph AC, Dorst J.

Acta Neurol Scand. 2017 Sep;136(3):204-211. doi: 10.1111/ane.12713. Epub 2016 Nov 15.

PMID:
27858953
14.

MUC1-ARF-A Novel MUC1 Protein That Resides in the Nucleus and Is Expressed by Alternate Reading Frame Translation of MUC1 mRNA.

Chalick M, Jacobi O, Pichinuk E, Garbar C, Bensussan A, Meeker A, Ziv R, Zehavi T, Smorodinsky NI, Hilkens J, Hanisch FG, Rubinstein DB, Wreschner DH.

PLoS One. 2016 Oct 21;11(10):e0165031. doi: 10.1371/journal.pone.0165031. eCollection 2016.

15.

Reduced hnRNPA3 increases C9orf72 repeat RNA levels and dipeptide-repeat protein deposition.

Mori K, Nihei Y, Arzberger T, Zhou Q, Mackenzie IR, Hermann A, Hanisch F; German Consortium for Frontotemporal Lobar Degeneration; Bavarian Brain Banking Alliance, Kamp F, Nuscher B, Orozco D, Edbauer D, Haass C.

EMBO Rep. 2016 Sep;17(9):1314-25. doi: 10.15252/embr.201541724. Epub 2016 Jul 26.

16.

Functional consequence of fibulin-4 missense mutations associated with vascular and skeletal abnormalities and cutis laxa.

Sasaki T, Hanisch FG, Deutzmann R, Sakai LY, Sakuma T, Miyamoto T, Yamamoto T, Hannappel E, Chu ML, Lanig H, von der Mark K.

Matrix Biol. 2016 Dec;56:132-149. doi: 10.1016/j.matbio.2016.06.003. Epub 2016 Jun 23.

PMID:
27339457
17.

Human Norovirus Interactions with Histo-Blood Group Antigens and Human Milk Oligosaccharides.

Schroten H, Hanisch FG, Hansman GS.

J Virol. 2016 Jun 10;90(13):5855-5859. doi: 10.1128/JVI.00317-16. Print 2016 Jul 1. Review.

18.

Differential Proteomics of Urinary Exovesicles from Classical Galactosemic Patients Reveals Subclinical Kidney Insufficiency.

Staubach S, Pekmez M, Hanisch FG.

J Proteome Res. 2016 Jun 3;15(6):1754-61. doi: 10.1021/acs.jproteome.5b00902. Epub 2016 May 11.

PMID:
27103203
19.

Neutral glycans from sandfish skin can reduce friction of polymers.

Vihar B, Hanisch FG, Baumgartner W.

J R Soc Interface. 2016 Mar;13(116). pii: 20160103. doi: 10.1098/rsif.2016.0103.

20.

Titin antibodies in "seronegative" myasthenia gravis--A new role for an old antigen.

Stergiou C, Lazaridis K, Zouvelou V, Tzartos J, Mantegazza R, Antozzi C, Andreetta F, Evoli A, Deymeer F, Saruhan-Direskeneli G, Durmus H, Brenner T, Vaknin A, Berrih-Aknin S, Behin A, Sharshar T, De Baets M, Losen M, Martinez-Martinez P, Kleopa KA, Zamba-Papanicolaou E, Kyriakides T, Kostera-Pruszczyk A, Szczudlik P, Szyluk B, Lavrnic D, Basta I, Peric S, Tallaksen C, Maniaol A, Gilhus NE, Casasnovas Pons C, Pitha J, Jakubíkova M, Hanisch F, Bogomolovas J, Labeit D, Labeit S, Tzartos SJ.

J Neuroimmunol. 2016 Mar 15;292:108-15. doi: 10.1016/j.jneuroim.2016.01.018. Epub 2016 Jan 27.

PMID:
26943968
21.

Needle electromyography findings in patients with MATR3 mutation - A prospective study.

Hanisch F, Kraya T, Müller T, Kornhuber M.

Clin Neurophysiol. 2016 Apr;127(4):2085-6. doi: 10.1016/j.clinph.2015.12.008. Epub 2015 Dec 18. No abstract available.

PMID:
26899464
22.

Functional Analysis of the Glucuronyltransferases GlcAT-P and GlcAT-S of Drosophila melanogaster: Distinct Activities towards the O-linked T-antigen.

Breloy I, Schwientek T, Althoff D, Holz M, Koppen T, Krupa A, Hanisch FG.

Biomolecules. 2016 Jan 6;6(1):8. doi: 10.3390/biom6010008.

23.

Clinical features and differential diagnosis of flail arm syndrome.

Hübers A, Hildebrandt V, Petri S, Kollewe K, Hermann A, Storch A, Hanisch F, Zierz S, Rosenbohm A, Ludolph AC, Dorst J.

J Neurol. 2016 Feb;263(2):390-395. doi: 10.1007/s00415-015-7993-z. Epub 2015 Dec 24.

PMID:
26705123
24.

VCP and PSMF1: Antagonistic regulators of proteasome activity.

Clemen CS, Marko M, Strucksberg KH, Behrens J, Wittig I, Gärtner L, Winter L, Chevessier F, Matthias J, Türk M, Tangavelou K, Schütz J, Arhzaouy K, Klopffleisch K, Hanisch FG, Rottbauer W, Blümcke I, Just S, Eichinger L, Hofmann A, Schröder R.

Biochem Biophys Res Commun. 2015 Aug 7;463(4):1210-7. doi: 10.1016/j.bbrc.2015.06.086. Epub 2015 Jun 15.

25.

MuSK autoantibodies in myasthenia gravis detected by cell based assay--A multinational study.

Tsonis AI, Zisimopoulou P, Lazaridis K, Tzartos J, Matsigkou E, Zouvelou V, Mantegazza R, Antozzi C, Andreetta F, Evoli A, Deymeer F, Saruhan-Direskeneli G, Durmus H, Brenner T, Vaknin A, Berrih-Aknin S, Behin A, Sharshar T, De Baets M, Losen M, Martinez-Martinez P, Kleopa KA, Zamba-Papanicolaou E, Kyriakides T, Kostera-Pruszczyk A, Szczudlik P, Szyluk B, Lavrnic D, Basta I, Peric S, Tallaksen C, Maniaol A, Casasnovas Pons C, Pitha J, Jakubíkova M, Hanisch F, Tzartos SJ.

J Neuroimmunol. 2015 Jul 15;284:10-7. doi: 10.1016/j.jneuroim.2015.04.015. Epub 2015 Apr 27.

PMID:
26025053
26.
27.

Impairment of respiratory function in late-onset distal myopathy due to MATR3 Mutation.

Kraya T, Schmidt B, Müller T, Hanisch F.

Muscle Nerve. 2015 Jun;51(6):916-8. doi: 10.1002/mus.24603.

PMID:
25677933
28.

Characterization of monoclonal gammopathy in patients with amyotrophic lateral sclerosis.

Wolf HH, Posa A, Panitz S, Kornhuber M, Hanisch F.

Acta Neurol Scand. 2015 Sep;132(3):212-5. doi: 10.1111/ane.12377. Epub 2015 Feb 3.

PMID:
25644365
29.

Characteristics of pain in amyotrophic lateral sclerosis.

Hanisch F, Skudlarek A, Berndt J, Kornhuber ME.

Brain Behav. 2015 Mar;5(3):e00296. doi: 10.1002/brb3.296. Epub 2015 Jan 21.

30.

The checklist individual strength (CIS20-R) in patients with amyotrophic lateral sclerosis - a longitudinal study.

Panitz S, Kornhuber M, Hanisch F.

Acta Neurol Scand. 2015 Jun;131(6):372-80. doi: 10.1111/ane.12349. Epub 2015 Jan 7.

PMID:
25639482
31.

Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study.

Dorst J, Dupuis L, Petri S, Kollewe K, Abdulla S, Wolf J, Weber M, Czell D, Burkhardt C, Hanisch F, Vielhaber S, Meyer T, Frisch G, Kettemann D, Grehl T, Schrank B, Ludolph AC.

J Neurol. 2015;262(4):849-58. doi: 10.1007/s00415-015-7646-2. Epub 2015 Jan 25.

PMID:
25618254
32.

Morphology and function of cerebral arteries in adults with pompe disease.

Hensel O, Hanisch F, Stock K, Stoevesandt D, Deschauer M, Müller T.

JIMD Rep. 2015;20:27-33. doi: 10.1007/8904_2014_385. Epub 2015 Jan 23.

33.

Obstetric risk in patients with myopathy due to MATR3 mutations.

Mueller T, Berndt J, Hanisch F.

Mol Genet Metab Rep. 2014 Dec 4;2:32-33. doi: 10.1016/j.ymgmr.2014.11.008. eCollection 2015 Mar.

34.

Functional relevance of mitochondrial abnormalities in sporadic inclusion body myositis.

Joshi PR, Vetterke M, Hauburger A, Tacik P, Stoltenburg G, Hanisch F.

J Clin Neurosci. 2014 Nov;21(11):1959-63. doi: 10.1016/j.jocn.2014.05.051. Epub 2014 Oct 11.

PMID:
25311418
35.

Trefoil factor family domains represent highly efficient conformational determinants for N-linked N,N'-di-N-acetyllactosediamine (LacdiNAc) synthesis.

Bonar D, Hanisch FG.

J Biol Chem. 2014 Oct 24;289(43):29677-90. doi: 10.1074/jbc.M114.596049. Epub 2014 Sep 10.

36.

Urge incontinence and gastrointestinal symptoms in adult patients with pompe disease: a cross-sectional survey.

Karabul N, Skudlarek A, Berndt J, Kornblum C, Kley RA, Wenninger S, Tiling N, Mengel E, Plöckinger U, Vorgerd M, Deschauer M, Schoser B, Hanisch F.

JIMD Rep. 2014;17:53-61. doi: 10.1007/8904_2014_334. Epub 2014 Aug 26.

37.

Phenotype of matrin-3-related distal myopathy in 16 German patients.

Müller TJ, Kraya T, Stoltenburg-Didinger G, Hanisch F, Kornhuber M, Stoevesandt D, Senderek J, Weis J, Baum P, Deschauer M, Zierz S.

Ann Neurol. 2014 Nov;76(5):669-80. doi: 10.1002/ana.24255. Epub 2014 Sep 16.

PMID:
25154462
38.

SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions.

Hanisch F, Kornhuber M, Alston CL, Taylor RW, Deschauer M, Zierz S.

J Neurol Neurosurg Psychiatry. 2015 Jun;86(6):630-4. doi: 10.1136/jnnp-2013-306748. Epub 2014 Aug 20.

PMID:
25143630
39.

Human trefoil factor 2 is a lectin that binds α-GlcNAc-capped mucin glycans with antibiotic activity against Helicobacter pylori.

Hanisch FG, Bonar D, Schloerer N, Schroten H.

J Biol Chem. 2014 Oct 3;289(40):27363-75. doi: 10.1074/jbc.M114.597757. Epub 2014 Aug 14.

40.

Novel recessive myotilin mutation causes severe myofibrillar myopathy.

Schessl J, Bach E, Rost S, Feldkirchner S, Kubny C, Müller S, Hanisch FG, Kress W, Schoser B.

Neurogenetics. 2014 Aug;15(3):151-6. doi: 10.1007/s10048-014-0410-4. Epub 2014 Jun 14.

PMID:
24928145
41.

Limb girdle muscular dystrophy type 2L presenting as necrotizing myopathy.

Schneider I, Stoltenburg G, Deschauer M, Winterholler M, Hanisch F.

Acta Myol. 2014 May;33(1):19-21.

42.

Enzyme replacement therapy and antibodies in late-onset Pompe disease.

Schneider I, Deschauer M, Hanisch F.

Mol Genet Metab Rep. 2014 May 15;1:232-234. eCollection 2014. No abstract available.

43.

Eosinophils in hereditary and inflammatory myopathies.

Schröder T, Fuchss J, Schneider I, Stoltenburg-Didinger G, Hanisch F.

Acta Myol. 2013 Dec;32(3):148-53.

44.

Pregnancy and delivery in women with Pompe disease.

Karabul N, Berndt J, Kornblum C, Kley RA, Wenninger S, Tiling N, Mengel E, Plöckinger U, Vorgerd M, Deschauer M, Schoser B, Hanisch F.

Mol Genet Metab. 2014 Jun;112(2):148-53. doi: 10.1016/j.ymgme.2014.03.010. Epub 2014 Mar 30.

PMID:
24726296
45.

Porcine gastric TFF2 is a mucus constituent and differs from pancreatic TFF2.

Stürmer R, Müller S, Hanisch FG, Hoffmann W.

Cell Physiol Biochem. 2014;33(4):895-904. doi: 10.1159/000358662. Epub 2014 Mar 28.

46.

Pain in adult patients with Pompe disease.

Karabul N, Kruijshaar ME, Schober A, Güngör D, Hanisch F.

Mol Genet Metab Rep. 2014 Apr 2;1:139-140. eCollection 2014. No abstract available.

47.

Pseudo-Popeye syndrome: extramedullary plasmacytoma manifesting in skeletal muscle.

Schneider I, Müller T, Stoltenburg G, Holzhausen HJ, Mawrin C, Hanisch F.

Neurology. 2014 Feb 11;82(6):544-5. doi: 10.1212/WNL.0000000000000099. No abstract available.

PMID:
24514010
48.

Risk factors for osteoporosis, falls and fractures in hereditary myopathies and sporadic inclusion body myositis - A cross sectional survey.

Danckworth F, Karabul N, Posa A, Hanisch F.

Mol Genet Metab Rep. 2014 Feb 11;1:85-97. eCollection 2014.

49.

Glycogenosome accumulation in the arrector pili muscle in Pompe disease.

Katona I, Weis J, Hanisch F.

Orphanet J Rare Dis. 2014 Feb 5;9:17. doi: 10.1186/1750-1172-9-17.

50.

The significance of pathological spontaneous activity in various myopathies.

Hanisch F, Kronenberger C, Zierz S, Kornhuber M.

Clin Neurophysiol. 2014 Jul;125(7):1485-90. doi: 10.1016/j.clinph.2013.11.021. Epub 2013 Dec 2.

PMID:
24370491

Supplemental Content

Loading ...
Support Center