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Gene|March 16, 2015
Single nucleotide polymorphism creating a variable upstream open reading frame regulates glucocorticoid receptor expressionClaudia Marceca, Martina Pfob, Gustav Schelling, et al.Neurogenetics|December 17, 2002
Congenital myasthenia in Brahman calves caused by homozygosity for a CHRNE truncating mutationSimone Kraner, Jörn P Sieb, Peter N Thompson, et al.Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|March 15, 2018
Birt-Hogg-Dubé-Syndrom: ein zu selten diagnostiziertes erbliches TumorsyndromOrtrud K Steinlein, Birgit Ertl-Wagner, Thomas Ruzicka, et al.Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|March 15, 2018
Birt-Hogg-Dubé syndrome: an underdiagnosed genetic tumor syndromeOrtrud K Steinlein, Birgit Ertl-Wagner, Thomas Ruzicka, et al.Cancer Letters|November 19, 2015
DICER1 syndrome can mimic different genetic tumor predispositionsYasmin Mehraein, Irene Schmid, Marlene Eggert, et al.Plos One|July 12, 2013
Nicotinic acetylcholine receptor subunits α4 and α5 associated with smoking behaviour and lung cancer are regulated by upstream open reading framesMarlene Eggert, Eric Aichinger, Michael W Pfaffl, et al.European Journal of Cancer (Oxford, England : 1990)|May 17, 2021
Colorectal cancer risk in families with Birt-Hogg-Dubé syndrome increasedElke C Sattler, Zulfiya Syunyaeva, Marlene Reithmair, et al.Epilepsia|March 22, 2002
Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24Eylert Brodtkorb, Wenli Gu, Karl O Nakken, et al.Epilepsy Research|August 23, 2005
A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsyWenli Gu, Thomas Sander, Armin Heils, et al.Epilepsy Research|July 26, 2005
Neonatal seizures with tonic clonic sequences and poor developmental outcomeBernhard Schmitt, Gabriele Wohlrab, Thomas Sander, et al.Pageof 8