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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 2
2003 1
2004 3
2005 2
2006 3
2007 3
2008 1
2009 3
2010 2
2011 3
2012 1
2013 4
2014 2
2015 5
2016 2
2017 5
2018 3
2019 2
2020 12
2021 1
2022 6
2023 3
2024 3

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68 results

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Page 1
Derivation and expansion using only small molecules of human neural progenitors for neurodegenerative disease modeling.
Reinhardt P, Glatza M, Hemmer K, Tsytsyura Y, Thiel CS, Höing S, Moritz S, Parga JA, Wagner L, Bruder JM, Wu G, Schmid B, Röpke A, Klingauf J, Schwamborn JC, Gasser T, Schöler HR, Sterneckert J. Reinhardt P, et al. Among authors: ropke a. PLoS One. 2013;8(3):e59252. doi: 10.1371/journal.pone.0059252. Epub 2013 Mar 22. PLoS One. 2013. PMID: 23533608 Free PMC article.
Gastrointestinal stromal tumor presenting as a rectovaginal mass. Clinicopathologic and molecular-genetic characterization of a rare tumor with a literature review.
Pelz AF, Agaimy A, Daniels M, Evert M, Schulz HU, Lüders P, Müller G, Lasota J, Röpke A, Wieacker P, Miettinen M, Schneider-Stock R. Pelz AF, et al. Among authors: ropke a. Hum Pathol. 2011 Apr;42(4):586-93. doi: 10.1016/j.humpath.2010.08.007. Epub 2011 Jan 14. Hum Pathol. 2011. PMID: 21237497 Review.
Congenital Limb Defects: A Retrospective Cohort Study and Overview of the Literature.
Oelmeier K, Schmitz R, Dera I, Plaßmann M, Braun J, Willy D, Sourouni M, Köster HA, Steinhard J, Röpke A, Klockenbusch W, Möllers M. Oelmeier K, et al. Among authors: ropke a. Ultraschall Med. 2023 Oct;44(5):e241-e247. doi: 10.1055/a-1926-7201. Epub 2022 Oct 5. Ultraschall Med. 2023. PMID: 36198323 English.
Human fertilization in vivo and in vitro requires the CatSper channel to initiate sperm hyperactivation.
Young S, Schiffer C, Wagner A, Patz J, Potapenko A, Herrmann L, Nordhoff V, Pock T, Krallmann C, Stallmeyer B, Röpke A, Kierzek M, Biagioni C, Wang T, Haalck L, Deuster D, Hansen JN, Wachten D, Risse B, Behre HM, Schlatt S, Kliesch S, Tüttelmann F, Brenker C, Strünker T. Young S, et al. Among authors: ropke a. J Clin Invest. 2024 Jan 2;134(1):e173564. doi: 10.1172/JCI173564. J Clin Invest. 2024. PMID: 38165034 Free PMC article.
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
Okutman O, Muller J, Skory V, Garnier JM, Gaucherot A, Baert Y, Lamour V, Serdarogullari M, Gultomruk M, Röpke A, Kliesch S, Herbepin V, Aknin I, Benkhalifa M, Teletin M, Bakircioglu E, Goossens E, Charlet-Berguerand N, Bahceci M, Tüttelmann F, Viville S. Okutman O, et al. Among authors: ropke a. J Assist Reprod Genet. 2017 May;34(5):683-694. doi: 10.1007/s10815-017-0900-z. Epub 2017 Apr 11. J Assist Reprod Genet. 2017. PMID: 28401488 Free PMC article.
68 results