Rauschendorf MA - Search Results

1

Determination of endometrial cancer molecular subtypes using a whole exome-sequencing based single-method approach.

Mustea A, Ralser DJ, Egger EK, Ziehm U, Vivas S, Brock S, Jackson D, Condic M, Rauschendorf MA, Würfel P, Dombrowski F, Otten LA, Sun P, Laib A, Cordova MC, Hartmann R, Stein MA, Koensgen D, Stope MB. Mustea A, et al. Among authors: rauschendorf ma. J Cancer Res Clin Oncol. 2024 Jul 25;150(7):367. doi: 10.1007/s00432-024-05901-4. J Cancer Res Clin Oncol. 2024. PMID: 39052171 Free PMC article.

2

AZFa Y gene, DDX3Y, evolved novel testis transcript variants in primates with proximal 3´UTR polyadenylation for germ cell specific translation.

Vogt PH, Rauschendorf MA, Zimmer J, Drummer C, Behr R. Vogt PH, et al. Among authors: rauschendorf ma. Sci Rep. 2022 May 27;12(1):8954. doi: 10.1038/s41598-022-12474-0. Sci Rep. 2022. PMID: 35624115 Free PMC article.

3

Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome.

Epanchintsev A, Rauschendorf MA, Costanzo F, Calmels N, Obringer C, Sarasin A, Coin F, Laugel V, Egly JM. Epanchintsev A, et al. Among authors: rauschendorf ma. Sci Rep. 2020 Jan 24;10(1):1105. doi: 10.1038/s41598-020-57999-4. Sci Rep. 2020. PMID: 31980658 Free PMC article.

4

Homozygous intronic MITF mutation causes severe Waardenburg syndrome type 2A.

Rauschendorf MA, Zimmer AD, Laut A, Demmer P, Rösler B, Happle R, Sartori S, Fischer J. Rauschendorf MA, et al. Pigment Cell Melanoma Res. 2019 Jan;32(1):85-91. doi: 10.1111/pcmr.12733. Epub 2018 Sep 6. Pigment Cell Melanoma Res. 2019. PMID: 30117279 No abstract available.

5

Cockayne's Syndrome A and B Proteins Regulate Transcription Arrest after Genotoxic Stress by Promoting ATF3 Degradation.

Epanchintsev A, Costanzo F, Rauschendorf MA, Caputo M, Ye T, Donnio LM, Proietti-de-Santis L, Coin F, Laugel V, Egly JM. Epanchintsev A, et al. Among authors: rauschendorf ma. Mol Cell. 2017 Dec 21;68(6):1054-1066.e6. doi: 10.1016/j.molcel.2017.11.009. Epub 2017 Dec 7. Mol Cell. 2017. PMID: 29225035 Free article.

6

Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis.

Hotz A, Fagerberg C, Vahlquist A, Bygum A, Törmä H, Rauschendorf MA, Zhang H, Heinz L, Bourrat E, Hausser I, Vestergaard V, Dragomir A, Zimmer AD, Fischer J. Hotz A, et al. Among authors: rauschendorf ma. Br J Dermatol. 2018 Mar;178(3):e207-e209. doi: 10.1111/bjd.15994. Epub 2018 Jan 21. Br J Dermatol. 2018. PMID: 28906551 No abstract available.

7

Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans.

Heinz L, Kim GJ, Marrakchi S, Christiansen J, Turki H, Rauschendorf MA, Lathrop M, Hausser I, Zimmer AD, Fischer J. Heinz L, et al. Among authors: rauschendorf ma. Am J Hum Genet. 2017 Jun 1;100(6):926-939. doi: 10.1016/j.ajhg.2017.05.007. Am J Hum Genet. 2017. PMID: 28575648 Free PMC article.

8

Novel compound heterozygous synaptojanin-1 mutation causes l-dopa-responsive dystonia-parkinsonism syndrome.

Rauschendorf MA, Jost M, Stock F, Zimmer A, Rösler B, Rijntjes M, Piroth T, Coenen VA, Reinacher PC, Meyer PT, Frings L, Weiller C, Fischer J, Klebe S. Rauschendorf MA, et al. Mov Disord. 2017 Mar;32(3):478-480. doi: 10.1002/mds.26876. Epub 2016 Nov 21. Mov Disord. 2017. PMID: 27869329 No abstract available.

9

DDX3X, the X homologue of AZFa gene DDX3Y, expresses a complex pattern of transcript variants only in the male germ line.

Rauschendorf MA, Zimmer J, Ohnmacht C, Vogt PH. Rauschendorf MA, et al. Mol Hum Reprod. 2014 Dec;20(12):1208-22. doi: 10.1093/molehr/gau081. Epub 2014 Sep 10. Mol Hum Reprod. 2014. PMID: 25208899

10

Regulatory interplay of Cockayne syndrome B ATPase and stress-response gene ATF3 following genotoxic stress.

Kristensen U, Epanchintsev A, Rauschendorf MA, Laugel V, Stevnsner T, Bohr VA, Coin F, Egly JM. Kristensen U, et al. Among authors: rauschendorf ma. Proc Natl Acad Sci U S A. 2013 Jun 18;110(25):E2261-70. doi: 10.1073/pnas.1220071110. Epub 2013 Jun 3. Proc Natl Acad Sci U S A. 2013. PMID: 23733932 Free PMC article.

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