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Günter Assum

Research Profile

Genes & Molecular Sequences

Disorders

Neurofibromatosis 1

Chemicals & Drugs

Concepts & Ideas

Anatomy

Procedures

Physiology

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Publications

TOP 3
Rudolf Reiter; Anke Schwandt; Walther Vogel; Anja Pickhard; Günter Assum; Sibylle Brosch; Elena Fischbein; Stephan Haase; Josef Högel; Manuel Lüdeke; Christiane Maier
Genetic and environmental risk factors for submucous cleft palate.
Fulvio Cruciani; Beniamino Trombetta; Cheyenne Antonelli; Roberto Pascone; Guido Valesini; Valentina Scalzi; Giuseppe Vona; Béla Melegh; Boris Zagradisnik; Günter Assum; Georgi D Efremov; Daniele Sellitto; Rosaria Scozzari
Strong intra- and inter-continental differentiation revealed by Y chromosome SNPs M269, U106 and U152.
Silvia Kastler; Lisa Honold; Manuel Luedeke; Rainer Kuefer; Peter Möller; Josef Hoegel; Walther Vogel; Christiane Maier; Günter Assum
POU5F1P1, a putative cancer susceptibility gene, is overexpressed in prostatic carcinoma.

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All Publications

2012: Rudolf Reiter; Anke Schwandt; Walther Vogel; Anja Pickhard; Günter Assum; Sibylle Brosch; Elena Fischbein; Stephan Haase; Josef Högel; Manuel Lüdeke; Christiane Maier
Genetic and environmental risk factors for submucous cleft palate.
European journal of oral sciences 2012;120(2):97-103.
2011: Fulvio Cruciani; Beniamino Trombetta; Cheyenne Antonelli; Roberto Pascone; Guido Valesini; Valentina Scalzi; Giuseppe Vona; Béla Melegh; Boris Zagradisnik; Günter Assum; Georgi D Efremov; Daniele Sellitto; Rosaria Scozzari
Strong intra- and inter-continental differentiation revealed by Y chromosome SNPs M269, U106 and U152.
Forensic science international. Genetics 2011;5(3):e49-52.
2010: Silvia Kastler; Lisa Honold; Manuel Luedeke; Rainer Kuefer; Peter Möller; Josef Hoegel; Walther Vogel; Christiane Maier; Günter Assum
POU5F1P1, a putative cancer susceptibility gene, is overexpressed in prostatic carcinoma.
The Prostate 2010;70(6):666-74.
2008: Natascha Bachmann; Juergen Haeusler; Manuel Luedeke; Rainer Kuefer; Sven Perner; Günter Assum; Thomas Paiss; Josef Hoegel; Walther Vogel; Christiane Maier
Expression changes of CAV1 and EZH2, located on 7q31 approximately q36, are rarely related to genomic alterations in primary prostate carcinoma.
Cancer genetics and cytogenetics 2008;182(2):103-10.
2008: Johannes Stökl; Philipp M Schlüter; Tod F Stuessy; Hannes F Paulus; Günter Assum; Manfred Ayasse
Scent variation and hybridization cause the displacement of a sexually deceptive orchid species.
American journal of botany 2008;95(4):472-81.
2007: Fulvio Cruciani; Roberta La Fratta; Beniamino Trombetta; Piero Santolamazza; Daniele Sellitto; Eliane Beraud Colomb; Jean-Michel Dugoujon; Federica Crivellaro; Tamara Benincasa; Roberto Pascone; Pedro Moral; Elizabeth Watson; Béla Melegh; Guido Barbujani; Silvia Fuselli; Giuseppe Vona; Boris Zagradisnik; Günter Assum; Radim Brdicka; Andrey I Kozlov; Georgi D Efremov; Alfredo Coppa; Andrea Novelletto; Rosaria Scozzari
Tracing past human male movements in northern/eastern Africa and western Eurasia: new clues from Y-chromosomal haplogroups E-M78 and J-M12.
Molecular biology and evolution 2007;24(6):1300-11.
2007: Claudia Schmegner; Josef Hoegel; Walther Vogel; Günter Assum
A comparison of the variability spectra of two genomic loci in a European group of individuals reveals fundamental differences pointing to selection or a population bottleneck.
Annals of human genetics 2007;71(Pt 3):370-8.
2007: Claudia Schmegner; Horst Hameister; Walther Vogel; Günter Assum
Isochores and replication time zones: a perfect match.
Cytogenetic and genome research 2007;116(3):167-72.
2007: Claudia Schmegner; Josef Hoegel; Walther Vogel; Günter Assum
The rate, not the spectrum, of base pair substitutions changes at a GC-content transition in the human NF1 gene region: implications for the evolution of the mammalian genome structure.
Genetics 2007;175(1):421-8.
2006: Christiane Maier; Zorica Vesovic; Natascha Bachmann; Kathleen Herkommer; Anja K Braun; Harald M Surowy; Günter Assum; Thomas Paiss; Walther Vogel
Germline mutations of the MSR1 gene in prostate cancer families from Germany.
Human mutation 2006;27(1):98-102.
2005: Claudia Schmegner; Josef Hoegel; Walther Vogel; Günter Assum
Genetic variability in a genomic region with long-range linkage disequilibrium reveals traces of a bottleneck in the history of the European population.
Human genetics 2005;118(2):276-86.
2005: Claudia Schmegner; Anke Berger; Walther Vogel; Horst Hameister; Günter Assum
An isochore transition zone in the NF1 gene region is a conserved landmark of chromosome structure and function.
Genomics 2005;86(4):439-45.
2003: Verena Wiest; Ingrid Eisenbarth; Claudia Schmegner; Winfrid Krone; Günter Assum
Somatic NF1 mutation spectra in a family with neurofibromatosis type 1: toward a theory of genetic modifiers.
Human mutation 2003;22(6):423-7.
2002: Hildegard Kehrer-Sawatzki; Günter Assum; Horst Hameister
Molecular characterisation of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication.
Human genetics 2002;111(4-5):465-7; author reply 468-9.
2002: Christiane Maier; K Rösch; Kathleen Herkommer; Sylvia Bochum; G Cancel-Tassin; Olivier Cussenot; Jürgen Häussler; Günter Assum; Walther Vogel; Thomas Paiss
A candidate gene approach within the susceptibility region PCaP on 1q42.2-43 excludes deleterious mutations of the PCTA-1 gene to be responsible for hereditary prostate cancer.
European urology 2002;42(3):301-7.
2001: Dieter Kaufmann; Ralf Müller; Britta Bartelt; Michael Wolf; Karin Kunzi-Rapp; C Oliver Hanemann; R Fahsold; Christian Hein; Walther Vogel; Günter Assum
Spinal neurofibromatosis without café-au-lait macules in two families with null mutations of the NF1 gene.
American journal of human genetics 2001;69(6):1395-400.
2001: Ingrid Eisenbarth; A M Striebel; E Moschgath; Walther Vogel; Günter Assum
Long-range sequence composition mirrors linkage disequilibrium pattern in a 1.13 Mb region of human chromosome 22.
Human molecular genetics 2001;10(24):2833-9.
2000: Ingrid Eisenbarth; G Vogel; Winfrid Krone; Walther Vogel; Günter Assum
An isochore transition in the NF1 gene region coincides with a switch in the extent of linkage disequilibrium.
American journal of human genetics 2000;67(4):873-80.
2000: Ingrid Eisenbarth; K Beyer; Winfrid Krone; Günter Assum
Toward a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1.
American journal of human genetics 2000;66(2):393-401.
2000: Juergen Haeussler; Juergen Haeusler; A M Striebel; Günter Assum; Walther Vogel; Henry Furneaux; Winfrid Krone
Tumor antigen HuR binds specifically to one of five protein-binding segments in the 3'-untranslated region of the neurofibromin messenger RNA.
Biochemical and biophysical research communications 2000;267(3):726-32.
1999: Ingrid Eisenbarth; D König-Greger; Gudrun Wöhr; Hildegard Kehrer-Sawatzki; Günter Assum
Characterization of an alphoid subfamily located near p-arm sequences on human chromosome 22.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1999;7(1):65-9.
1998: Hildegard Kehrer-Sawatzki; Gudrun Wöhr; Werner Schempp; Ingrid Eisenbarth; Gotthold Barbi; Günter Assum
Mapping of members of the low-copy-number repetitive DNA sequence family chAB4 within the p arms of human acrocentric chromosomes: characterization of Robertsonian translocations.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1998;6(6):429-35.
1998: Günter Assum; JJ Pasantes; Birgitta Gläser; Werner Schempp; Gudrun Wöhr
Concerted evolution of members of the multisequence family chAB4 located on various nonhomologous chromosomes.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(1):58-63.
1997: Hildegard Kehrer-Sawatzki; T Schwickardt; Günter Assum; M Rocchi; Winfrid Krone
A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2.
Human genetics 1997;100(5-6):595-600.
1997: Ingrid Eisenbarth; Günter Assum; Dieter Kaufmann; Winfrid Krone
Evidence for the presence of the second allele of the neurofibromatosis type 1 gene in melanocytes derived from café au laitmacules of NF1 patients.
Biochemical and biophysical research communications 1997;237(1):138-41.
1997: Hildegard Kehrer-Sawatzki; M Udart; Winfrid Krone; R Baden; R Fahsold; G Thomas; B Schmucker; Günter Assum
Mutational analysis and expression studies of the neurofibromatosis type 2 (NF2) gene in a patient with a ring chromosome 22 and NF2.
Human genetics 1997;100(1):67-74.
1997: Klaus Däschner; Günter Assum; Ingrid Eisenbarth; Winfrid Krone; Sven Hoffmeyer; S Wortmann; B Heymer; Hildegard Kehrer-Sawatzki
Clonal origin of tumor cells in a plexiform neurofibroma with LOH in NF1 intron 38 and in dermal neurofibromas without LOH of the NF1 gene.
Biochemical and biophysical research communications 1997;234(2):346-50.
1997: Hildegard Kehrer-Sawatzki; Jürgen Häussler; Winfrid Krone; H Bode; Dieter E Jenne; K U Mehnert; U Tümmers; Günter Assum
The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions.
Human genetics 1997;99(2):237-47.
1996: Gudrun Wöhr; T Fink; Günter Assum
A palindromic structure in the pericentromeric region of various human chromosomes.
Genome research 1996;6(4):267-79.
1995: M Stark; Günter Assum; Winfrid Krone
Single-cell PCR performed with neurofibroma Schwann cells reveals the presence of both alleles of the neurofibromatosis type 1 (NF1) gene.
Human genetics 1995;96(5):619-23.
1995: Sven Hoffmeyer; Günter Assum; J Griesser; Dieter Kaufmann; Peter Nürnberg; Winfrid Krone
On unequal allelic expression of the neurofibromin gene in neurofibromatosis type 1.
Human molecular genetics 1995;4(8):1267-72.
1995: Ingrid Eisenbarth; Sven Hoffmeyer; Dieter Kaufmann; Günter Assum; Winfrid Krone
Analysis of an alternatively spliced exon of the neurofibromatosis type 1 gene in cultured melanocytes from patients with neurofibromatosis 1.
Archives of dermatological research 1995;287(5):413-6.
1994: Sven Hoffmeyer; Günter Assum; Dieter Kaufmann; K Schwenk; Winfrid Krone
A deletion in the 5'-region of the neurofibromatosis type 1 (NF1) gene.
Human genetics 1994;94(1):97-100.
1994: Günter Assum; C Gartmann; Werner Schempp; Gudrun Wöhr
Evolution of the chAB4 multisequence family in primates.
Genomics 1994;21(1):34-41.
1994: Sven Hoffmeyer; Günter Assum; Dieter Kaufmann; Winfrid Krone
Unequal expression of NF1 alleles.
Nature genetics 1994;6(4):331.
1994: Sven Hoffmeyer; Günter Assum
An RsaI polymorphism in the transcribed region of the neurofibromatosis (NF1)-gene.
Human genetics 1994;93(4):481-2.
1993: Günter Assum; T Fink; T Steinbeisser; K J Fisel
Analysis of human extrachromosomal DNA elements originating from different beta-satellite subfamilies.
Human genetics 1993;91(5):489-95.
1993: K Motejlek; D Schindler; Günter Assum; Winfrid Krone
Increased amount and contour length distribution of small polydisperse circular DNA (spcDNA) in Fanconi anemia.
Mutation research 1993;293(3):205-14.
1992: M Stark; Günter Assum; Dieter Kaufmann; H Kehrer; Winfrid Krone
Analysis of segregation and expression of an identified mutation at the neurofibromatosis type 1 locus.
Human genetics 1992;90(4):356-9.
1991: M Stark; Günter Assum; Winfrid Krone
A small deletion and an adjacent base exchange in a potential stem-loop region of the neurofibromatosis 1 gene.
Human genetics 1991;87(6):685-7.
1991: Günter Assum; T Fink; C Klett; B Lengl; M Schanbacher; S Uhl; Gudrun Wöhr
A new multisequence family in human.
Genomics 1991;11(2):397-409.
1991: K Motejlek; Günter Assum; Winfrid Krone; A K Kleinschmidt
The size of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TSC) differs from that in fibroblasts.
Human genetics 1991;87(1):6-10.
1989: Günter Assum; B Böckle; T Fink; U Dmochewitz; Winfrid Krone
Restriction analysis of chromosomal sequences homologous to single-copy fragments cloned from small polydisperse circular DNA (spcDNA).
Human genetics 1989;82(3):249-54.
1988: C Neidlinger; Günter Assum; Winfrid Krone; C Dietrich; R Hochsattel; G Klotz
Increased amounts of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TS)
Human genetics 1988;79(3):286-8.
1987: E Roschmann; Günter Assum; T Fink
RFLP detected with a 5'-bcr-gene-sequence (HGM8 provisional no. D22S11).
Nucleic acids research 1987;15(4):1883.