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Items: 25

1.

Utilization of a breast cancer risk assessment tool by internal medicine residents in a primary care clinic: impact of an educational program.

Yadav S, Hartkop S, Cardenas PY, Ladkany R, Halalau A, Shoichet S, Maddens M, Zakalik D.

BMC Cancer. 2019 Mar 14;19(1):228. doi: 10.1186/s12885-019-5418-6.

2.

Intramolecular domain dynamics regulate synaptic MAGUK protein interactions.

Rademacher N, Kuropka B, Kunde SA, Wahl MC, Freund C, Shoichet SA.

Elife. 2019 Mar 13;8. pii: e41299. doi: 10.7554/eLife.41299.

3.

Defective Synapse Maturation and Enhanced Synaptic Plasticity in Shank2 Δex7-/- Mice.

Wegener S, Buschler A, Stempel AV, Kang SJ, Lim CS, Kaang BK, Shoichet SA, Manahan-Vaughan D, Schmitz D.

eNeuro. 2018 Jul 10;5(3). pii: ENEURO.0398-17.2018. doi: 10.1523/ENEURO.0398-17.2018. eCollection 2018 May-Jun.

4.

Protein kinase C regulates AMPA receptor auxiliary protein Shisa9/CKAMP44 through interactions with neuronal scaffold PICK1.

Kunde SA, Rademacher N, Zieger H, Shoichet SA.

FEBS Open Bio. 2017 Aug 15;7(9):1234-1245. doi: 10.1002/2211-5463.12261. eCollection 2017 Sep.

5.

MPP2 is a postsynaptic MAGUK scaffold protein that links SynCAM1 cell adhesion molecules to core components of the postsynaptic density.

Rademacher N, Schmerl B, Lardong JA, Wahl MC, Shoichet SA.

Sci Rep. 2016 Oct 19;6:35283. doi: 10.1038/srep35283.

6.

Comparison of accuracy of physical examination findings in initial progress notes between paper charts and a newly implemented electronic health record.

Yadav S, Kazanji N, K C N, Paudel S, Falatko J, Shoichet S, Maddens M, Barnes MA.

J Am Med Inform Assoc. 2017 Jan;24(1):140-144. doi: 10.1093/jamia/ocw067. Epub 2016 Jun 29.

PMID:
27357831
7.

NOMA-GAP/ARHGAP33 regulates synapse development and autistic-like behavior in the mouse.

Schuster S, Rivalan M, Strauss U, Stoenica L, Trimbuch T, Rademacher N, Parthasarathy S, Lajkó D, Rosenmund C, Shoichet SA, Winter Y, Tarabykin V, Rosário M.

Mol Psychiatry. 2015 Sep;20(9):1120-31. doi: 10.1038/mp.2015.42. Epub 2015 Apr 14.

PMID:
25869807
8.

Synaptic MAGUK multimer formation is mediated by PDZ domains and promoted by ligand binding.

Rademacher N, Kunde SA, Kalscheuer VM, Shoichet SA.

Chem Biol. 2013 Aug 22;20(8):1044-54. doi: 10.1016/j.chembiol.2013.06.016.

9.

Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patients.

Kunde SA, Rademacher N, Tzschach A, Wiedersberg E, Ullmann R, Kalscheuer VM, Shoichet SA.

Hum Genet. 2013 Apr;132(4):461-71. doi: 10.1007/s00439-012-1260-5. Epub 2013 Jan 18.

PMID:
23329067
10.

Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2.

Schmeisser MJ, Ey E, Wegener S, Bockmann J, Stempel AV, Kuebler A, Janssen AL, Udvardi PT, Shiban E, Spilker C, Balschun D, Skryabin BV, Dieck St, Smalla KH, Montag D, Leblond CS, Faure P, Torquet N, Le Sourd AM, Toro R, Grabrucker AM, Shoichet SA, Schmitz D, Kreutz MR, Bourgeron T, Gundelfinger ED, Boeckers TM.

Nature. 2012 Apr 29;486(7402):256-60. doi: 10.1038/nature11015.

PMID:
22699619
11.

Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.

Lesch KP, Selch S, Renner TJ, Jacob C, Nguyen TT, Hahn T, Romanos M, Walitza S, Shoichet S, Dempfle A, Heine M, Boreatti-Hümmer A, Romanos J, Gross-Lesch S, Zerlaut H, Wultsch T, Heinzel S, Fassnacht M, Fallgatter A, Allolio B, Schäfer H, Warnke A, Reif A, Ropers HH, Ullmann R.

Mol Psychiatry. 2011 May;16(5):491-503. doi: 10.1038/mp.2010.29. Epub 2010 Mar 23.

PMID:
20308990
12.

Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization.

Shoichet SA, Waibel S, Endruhn S, Sperfeld AD, Vorwerk B, Müller I, Erdogan F, Ludolph AC, Ropers HH, Ullmann R.

Amyotroph Lateral Scler. 2009 Jun;10(3):162-9. doi: 10.1080/17482960802535001.

PMID:
18985462
13.

Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation.

Kalscheuer VM, FitzPatrick D, Tommerup N, Bugge M, Niebuhr E, Neumann LM, Tzschach A, Shoichet SA, Menzel C, Erdogan F, Arkesteijn G, Ropers HH, Ullmann R.

Hum Genet. 2007 May;121(3-4):501-9. Epub 2007 Jan 9.

PMID:
17211639
14.

PubMed vs. HighWire Press: a head-to-head comparison of two medical literature search engines.

Vanhecke TE, Barnes MA, Zimmerman J, Shoichet S.

Comput Biol Med. 2007 Sep;37(9):1252-8. Epub 2006 Dec 20.

PMID:
17184763
15.

A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome.

Budny B, Chen W, Omran H, Fliegauf M, Tzschach A, Wisniewska M, Jensen LR, Raynaud M, Shoichet SA, Badura M, Lenzner S, Latos-Bielenska A, Ropers HH.

Hum Genet. 2006 Sep;120(2):171-8. Epub 2006 Jun 17.

PMID:
16783569
16.

Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy.

Shoichet SA, Duprez L, Hagens O, Waetzig V, Menzel C, Herdegen T, Schweiger S, Dan B, Vamos E, Ropers HH, Kalscheuer VM.

Hum Genet. 2006 Jan;118(5):559-67. Epub 2005 Oct 25.

PMID:
16249883
17.

Haploinsufficiency of novel FOXG1B variants in a patient with severe mental retardation, brain malformations and microcephaly.

Shoichet SA, Kunde SA, Viertel P, Schell-Apacik C, von Voss H, Tommerup N, Ropers HH, Kalscheuer VM.

Hum Genet. 2005 Oct;117(6):536-44. Epub 2005 Aug 17.

PMID:
16133170
18.

Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation.

Kalscheuer VM, Freude K, Musante L, Jensen LR, Yntema HG, Gécz J, Sefiani A, Hoffmann K, Moser B, Haas S, Gurok U, Haesler S, Aranda B, Nshedjan A, Tzschach A, Hartmann N, Roloff TC, Shoichet S, Hagens O, Tao J, Van Bokhoven H, Turner G, Chelly J, Moraine C, Fryns JP, Nuber U, Hoeltzenbein M, Scharff C, Scherthan H, Lenzner S, Hamel BC, Schweiger S, Ropers HH.

Nat Genet. 2003 Dec;35(4):313-5. Epub 2003 Nov 23.

PMID:
14634649
19.

Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.

Shoichet SA, Hoffmann K, Menzel C, Trautmann U, Moser B, Hoeltzenbein M, Echenne B, Partington M, Van Bokhoven H, Moraine C, Fryns JP, Chelly J, Rott HD, Ropers HH, Kalscheuer VM.

Am J Hum Genet. 2003 Dec;73(6):1341-54. Epub 2003 Nov 18.

20.

Frataxin promotes antioxidant defense in a thiol-dependent manner resulting in diminished malignant transformation in vitro.

Shoichet SA, Bäumer AT, Stamenkovic D, Sauer H, Pfeiffer AF, Kahn CR, Müller-Wieland D, Richter C, Ristow M.

Hum Mol Genet. 2002 Apr 1;11(7):815-21.

PMID:
11929854
21.

Transcriptional repression and developmental functions of the atypical vertebrate GATA protein TRPS1.

Malik TH, Shoichet SA, Latham P, Kroll TG, Peters LL, Shivdasani RA.

EMBO J. 2001 Apr 2;20(7):1715-25.

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Thrombocytopenia in a prospective, randomized, double-blind trial of bovine and porcine heparin.

Green D, Martin GJ, Shoichet SH, DeBacker N, Bomalaski JS, Lind RN.

Am J Med Sci. 1984 Sep;288(2):60-4.

PMID:
6385701
25.

Predisposing factors for pulmonary embolism.

Martin GJ, Shoichet S, Martin HG.

Ann Intern Med. 1981 Dec;95(6):781. No abstract available.

PMID:
7305164

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