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Gerd Scherer

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Frédéric Chalmel; Philippe Demougin; I Georg; Bernard Jégou; Aurélie Lardenois; Francisco Barrionuevo; Gerd Scherer; Michael Primig
Genome-wide identification of Sox8-, and Sox9-dependent genes during early post-natal testis development in the mouse.
Ina Georg; Francisco Barrionuevo; Thorsten Wiech; Gerd Scherer
Sox9 and Sox8 are required for basal lamina integrity of testis cords and for suppression of FOXL2 during embryonic testis development in mice.
Francisco Barrionuevo; Gerd Scherer
SOX E genes: SOX9 and SOX8 in mammalian testis development.

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All Publications

2013: Frédéric Chalmel; Philippe Demougin; I Georg; Bernard Jégou; Aurélie Lardenois; Francisco Barrionuevo; Gerd Scherer; Michael Primig
Genome-wide identification of Sox8-, and Sox9-dependent genes during early post-natal testis development in the mouse.
Andrology 2013;1(2):281-92.
2012: Ina Georg; Francisco Barrionuevo; Thorsten Wiech; Gerd Scherer
Sox9 and Sox8 are required for basal lamina integrity of testis cords and for suppression of FOXL2 during embryonic testis development in mice.
Biology of reproduction 2012;87(4):99.
2010: Francisco Barrionuevo; Gerd Scherer
SOX E genes: SOX9 and SOX8 in mammalian testis development.
The international journal of biochemistry & cell biology 2010;42(3):433-6.
2010: I Georg; Stefan Bagheri-Fam; K C Knower; P Wieacker; Gerd Scherer; Vincent R Harley
Mutations of the SRY-responsive enhancer of SOX9 are uncommon in XY gonadal dysgenesis.
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2010;4(6):321-5.
2010: Gwang-Jin Kim; Ina Georg; Harry Scherthan; Matthias Merkenschlager; Florian Guillou; Gerd Scherer; Francisco Barrionuevo
Dicer is required for Sertoli cell function and survival.
The International journal of developmental biology 2010;54(5):867-75.
2009: Brigitte Moniot; Faustine Declosmenil; Francisco Barrionuevo; Gerd Scherer; Kosuke Aritake; Safia Malki; Laetitia Marzi; Anne Cohen-Solal; Ina Georg; Jürgen Klattig; Christoph Englert; Yuna Kim; Blanche Capel; Naomi Eguchi; Yoshihiro Urade; Brigitte Boizet-Bonhoure; Francis Poulat
The PGD2 pathway, independently of FGF9, amplifies SOX9 activity in Sertoli cells during male sexual differentiation.
Development (Cambridge, England) 2009;136(11):1813-21.
2009: Francisco Barrionuevo; Ina Georg; Harry Scherthan; Charlotte Lécureuil; Florian Guillou; Michael Wegner; Gerd Scherer
Testis cord differentiation after the sex determination stage is independent of Sox9 but fails in the combined absence of Sox9 and Sox8.
Developmental biology 2009;327(2):301-12.
2008: Ekkehart Lausch; Pia Hermanns; Henner F Farin; Yasemin Alanay; Sheila Unger; Sarah Nikkel; Christoph Steinwender; Gerd Scherer; Jürgen Spranger; Bernhard Zabel; Andreas Kispert; andrea superti-furga
TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndrome.
American journal of human genetics 2008;83(5):649-55.
2008: Francisco Barrionuevo; Angela Naumann; Stefan Bagheri-Fam; Volker Speth; Makoto M Taketo; Gerd Scherer; Annette Neubüser
Sox9 is required for invagination of the otic placode in mice.
Developmental biology 2008;317(1):213-24.
2008: Stefan Bagheri-Fam; Helena Sim; Pascal Bernard; Irumini Jayakody; Makoto M Taketo; Gerd Scherer; Vincent R Harley
Loss of Fgfr2 leads to partial XY sex reversal.
Developmental biology 2008;314(1):71-83.
2007: Pauline Bastide; Charbel Darido; Julie Pannequin; Ralf Kist; Sylvie Robine; Christiane Marty-Double; Frédéric Bibeau; Gerd Scherer; Dominique Joubert; Frédéric Hollande; philippe blache; Philippe Jay
Sox9 regulates cell proliferation and is required for Paneth cell differentiation in the intestinal epithelium.
The Journal of cell biology 2007;178(4):635-48.
2007: Joy Lincoln; Ralf Kist; Gerd Scherer; Katherine E Yutzey
Sox9 is required for precursor cell expansion and extracellular matrix organization during mouse heart valve development.
Developmental biology 2007;305(1):120-32.
2007: Philip A Seymour; Kristine K Freude; Man N Tran; Erin E Mayes; Jan Jensen; Ralf Kist; Gerd Scherer; Maike Sander
SOX9 is required for maintenance of the pancreatic progenitor cell pool.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(6):1865-70.
2007: Michael Leipoldt; Martin Erdel; Gabriel A Bien-Willner; Marta Smyk; Markus Theurl; Svetlana A Yatsenko; James R Lupski; Andrew lane; Alan L Shanske; Pawel Stankiewicz; Gerd Scherer
Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia.
Clinical genetics 2007;71(1):67-75.
2006: Francisco Barrionuevo; Makoto M Taketo; Gerd Scherer; Andreas Kispert
Sox9 is required for notochord maintenance in mice.
Developmental biology 2006;295(1):128-40.
2006: Stefan Bagheri-Fam; Francisco Barrionuevo; Ulrike Dohrmann; Thomas Günther; Roland Schüle; Rolf Kemler; Moisés Mallo; Benoît Kanzler; Gerd Scherer
Long-range upstream and downstream enhancers control distinct subsets of the complex spatiotemporal Sox9 expression pattern.
Developmental biology 2006;291(2):382-97.
2006: Francisco Barrionuevo; Stefan Bagheri-Fam; Jürgen Klattig; Ralf Kist; Makoto M Taketo; Christoph Englert; Gerd Scherer
Homozygous inactivation of Sox9 causes complete XY sex reversal in mice.
Biology of reproduction 2006;74(1):195-201.
2005: Ramona Pop; Michael V Zaragoza; Mara Gaudette; Ulrike Dohrmann; Gerd Scherer
A homozygous nonsense mutation in SOX9 in the dominant disorder campomelic dysplasia: a case of mitotic gene conversion.
Human genetics 2005;117(1):43-53.
2005: Katherine L Hill-Harfe; Lee Kaplan; Heather J Stalker; Roberto T Zori; Ramona Pop; Gerd Scherer; Margaret R Wallace
Fine mapping of chromosome 17 translocation breakpoints > or = 900 Kb upstream of SOX9 in acampomelic campomelic dysplasia and a mild, familial skeletal dysplasia.
American journal of human genetics 2005;76(4):663-71.
2005: Anne-Karina T Perl; Ralf Kist; Zhengyuan Shan; Gerd Scherer; Jeffrey A Whitsett
Normal lung development and function after Sox9 inactivation in the respiratory epithelium.
Genesis (New York, N.Y. : 2000) 2005;41(1):23-32.
2004: Ramona Pop; C Conz; K S Lindenberg; Sophie Blesson; B Schmalenberger; Sylvain Briault; Dietmar Pfeifer; Gerd Scherer
Screening of the 1 Mb SOX9 5' control region by array CGH identifies a large deletion in a case of campomelic dysplasia with XY sex reversal.
Journal of medical genetics 2004;41(4):e47.
2002: Rongjia Zhou; Nathalie Bonneaud; Chao-Xing Yuan; Pascal de Santa Barbara; Brigitte Boizet; Tibor Schomber; Gerd Scherer; Robert G Roeder; Francis Poulat; Philippe Berta; Schomber Tibor
SOX9 interacts with a component of the human thyroid hormone receptor-associated protein complex.
Nucleic acids research 2002;30(14):3245-52.
2002: Ralf Kist; Heinrich Schrewe; Rudi Balling; Gerd Scherer
Conditional inactivation of Sox9: a mouse model for campomelic dysplasia.
Genesis (New York, N.Y. : 2000) 2002;32(2):121-3.
2002: Gerd Scherer
The molecular genetic jigsaw puzzle of vertebrate sex determination and its missing pieces.
Novartis Foundation symposium 2002;244():225-36; discussion 236-9, 253-7.
2001: Stefan Bagheri-Fam; C Ferraz; Jacques Demaille; Gerd Scherer; Dietmar Pfeifer
Comparative genomics of the SOX9 region in human and Fugu rubripes: conservation of short regulatory sequence elements within large intergenic regions.
Genomics 2001;78(1-2):73-82.
2001: Gerd Scherer; M Schmid
Genes and mechanisms in vertebrate sex determination. Introduction.
EXS 2001;(91):XI-XII.
2000: Brigitte Moniot; Philippe Berta; Gerd Scherer; P Südbeck; Francis Poulat
Male specific expression suggests role of DMRT1 in human sex determination.
Mechanisms of development 2000;91(1-2):323-5.
2000: Susanne Röttger; Katrin Schiebel; Gabriele Senger; S Ebner; Werner Schempp; Gerd Scherer
An SRY-negative 47,XXY mother and daughter.
Cytogenetics and cell genetics 2000;91(1-4):204-7.
2000: A Saridaki; C Ferraz; Jacques Demaille; Gerd Scherer; A F Roux
Genomic sequencing reveals the structure of the Kcnk6 and map3k11 genes and their close vicinity to the sipa1 gene on mouse chromosome 19.
Cytogenetics and cell genetics 2000;89(1-2):85-8.
2000: Dietmar Pfeifer; Francis Poulat; Elke Holinski-Feder; Frank Kooy; Gerd Scherer
The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome.
Genomics 2000;63(1):108-16.
1999: Dietmar Pfeifer; Ralf Kist; Ken Dewar; KL Devon; Eric S Lander; Bruce Birren; L Korniszewski; E Back; Gerd Scherer
Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region.
American journal of human genetics 1999;65(1):111-24.
1999: RA Pfeiffer; Anita Rauch; Udo Trautmann; Helmuth G Dörr; O Hiort; Gerd Scherer; G Rösch; Thomas Papadopoulos; K v d Hardt; E Lachmann
Defective sexual development in an infant with 46, XY, der(9)t(8;9)(q23.1;p23)mat.
European journal of pediatrics 1999;158(3):213-6.
1998: Pascal de Santa Barbara; Nathalie Bonneaud; Brigitte Boizet; M Desclozeaux; Brigitte Moniot; P Sudbeck; Gerd Scherer; Francis Poulat; Philippe Berta
Direct interaction of SRY-related protein SOX9 and steroidogenic factor 1 regulates transcription of the human anti-Müllerian hormone gene.
Molecular and cellular biology 1998;18(11):6653-65.
1998: Carsten M Pusch; E Hustert; Dietmar Pfeifer; P Südbeck; Ralf Kist; B Roe; Z Wang; Rudi Balling; nikolaus blin; Gerd Scherer
The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor.
Human genetics 1998;103(2):115-23.
1998: R Hühn; H Stoermer; B Klingele; E Bausch; A Fois; Maria Angela Farnetani; M Di Rocco; J Boué; J M Kirk; R Coleman; Gerd Scherer
Novel and recurrent tyrosine aminotransferase gene mutations in tyrosinemia type II.
Human genetics 1998;102(3):305-13.
1998: Gerd Scherer; M Held; Martin Erdel; D Meschede; J Horst; Ryszard Lesniewicz; Barbara Panasiuk
Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations.
Cytogenetics and cell genetics 1998;80(1-4):188-92.
1997: P Südbeck; Gerd Scherer
Two independent nuclear localization signals are present in the DNA-binding high-mobility group domains of SRY and SOX9.
The Journal of biological chemistry 1997;272(44):27848-52.
1997: J Becker-Follmann; A Gaa; E Baùsch; E Natt; Gerd Scherer; O von Deimling
High-resolution mapping of a linkage group on mouse chromosome 8 conserved on human chromosome 16Q.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(3):172-7.
1997: T Wagner; Niels Tommerup; Jutta Wirth; H Leffers; J Zimmer; E Back; J Weissenbach; Gerd Scherer
A somatic cell hybrid panel for distal 17q: GDIA1 maps to 17q25.3.
Cytogenetics and cell genetics 1997;76(3-4):172-5.
1997: J Meyer; P Südbeck; M Held; T Wagner; M L Schmitz; F D Bricarelli; E Eggermont; U Friedrich; O A Haas; A Kobelt; Jules G Leroy; Lionel Van Maldergem; E Michel; B Mitulla; RA Pfeiffer; Albert Schinzel; H Schmidt; Gerd Scherer
Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations.
Human molecular genetics 1997;6(1):91-8.
1996: P Südbeck; M Lienhard Schmitz; P A Baeuerle; Gerd Scherer
Sex reversal by loss of the C-terminal transactivation domain of human SOX9.
Nature genetics 1996;13(2):230-2.
1996: Jutta Wirth; T Wagner; J Meyer; RA Pfeiffer; H U Tietze; Werner Schempp; Gerd Scherer
Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9.
Human genetics 1996;97(2):186-93.
1996: J Meyer; Jutta Wirth; M Held; Werner Schempp; Gerd Scherer
SOX20, a new member of the SOX gene family, is located on chromosome 17p13.
Cytogenetics and cell genetics 1996;72(2-3):246-9.
1995: M Schmitt-Ney; H Thiele; P Kaltwasser; Barbara Bardoni; M Cisternino; Gerd Scherer
Two novel SRY missense mutations reducing DNA binding identified in XY females and their mosaic fathers.
American journal of human genetics 1995;56(4):862-9.
1994: U Matysiak-Scholze; Gerd Scherer
TaqI/ClaI polymorphism in the P4HB gene.
Human molecular genetics 1994;3(2):387.
1993: Barbara Panasiuk; Barbara Panasiuk; S Wołczyński; Gerd Scherer; U Matysiak-Scholze; R Leśniewicz; I Sipowicz
[Clinical examinations, chromosomal and molecular DNA in patients with Swyer syndrome].
Ginekologia polska 1993;64(5):257-62.
1992: R J Jäger; V R Harley; RA Pfeiffer; P N Goodfellow; Gerd Scherer
A familial mutation in the testis-determining gene SRY shared by both sexes.
Human genetics 1992;90(4):350-5.
1992: E Natt; K Kida; M Odievre; M Di Rocco; Gerd Scherer
Point mutations in the tyrosine aminotransferase gene in tyrosinemia type II.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(19):9297-301.
1992: U Wolf; Werner Schempp; Gerd Scherer
Molecular biology of the human Y chromosome.
Reviews of physiology, biochemistry and pharmacology 1992;121():147-213.
1990: R J Jäger; M Anvret; K Hall; Gerd Scherer
A human XY female with a frame shift mutation in the candidate testis-determining gene SRY.
Nature 1990;348(6300):452-4.
1990: R J Jäger; C Ebensperger; M Fraccaro; Gerd Scherer
A ZFY-negative 46,XX true hermaphrodite is positive for the Y pseudoautosomal boundary.
Human genetics 1990;85(6):666-8.
1990: Gerd Scherer; C T Bock; H Zentgraf
Heteroduplex between an EMBL3 genomic clone and a lambda gt11 cDNA clone provides internal size standards.
Nucleic acids research 1990;18(16):4944.
1990: R Rettenmeier; E Natt; H Zentgraf; Gerd Scherer
Isolation and characterization of the human tyrosine aminotransferase gene.
Nucleic acids research 1990;18(13):3853-61.
1989: Gerd Scherer; E Bausch; A Gaa; O von Deimling
Gene mapping on mouse chromosome 8 by interspecific crosses: new data on a linkage group conserved on human chromosome 16q.
Genomics 1989;5(2):275-82.
1989: Gerd Scherer; Werner Schempp; C Baccichetti; E Lenzini; Franca Dagna Bricarelli; L D Carbone; U Wolf
Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man.
Human genetics 1989;81(3):291-4.
1989: Gerd Scherer; Werner Schempp; M Fraccaro; E Bausch; V Bigozzi; P Maraschio; E Montali; G Simoni; U Wolf
Analysis of two 47,XXX males reveals X-Y interchange and maternal or paternal nondisjunction.
Human genetics 1989;81(3):247-51.
1989: Werner Schempp; G Müller; Gerd Scherer; S K Bohlander; W Rommerskirch; M Fraccaro; U Wolf
Localization of Y chromosome sequences and X chromosomal replication studies in XX males.
Human genetics 1989;81(2):144-8.
1989: E Natt; R Ellen Magenis; J Zimmer; A Mansouri; Gerd Scherer
Regional assignment of the human loci for uvomorulin (UVO) and chymotrypsinogen B (CTRB) with the help of two overlapping deletions on the long arm of chromosome 16.
Cytogenetics and cell genetics 1989;50(2-3):145-8.
1988: E M Westphal; E Natt; T Grimm; M Odievre; Gerd Scherer
The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II.
Human genetics 1988;79(3):260-4.
1987: E M Westphal; Margit Burmeister; T F Wienker; H Lehrach; K Bender; Gerd Scherer
Tyrosine aminotransferase and chymotrypsinogen B are linked to haptoglobin on human chromosome 16q: comparison of genetic and physical distances.
Genomics 1987;1(4):313-9.
1987: E Natt; E M Westphal; S E Toth-Fejel; R Ellen Magenis; N R Buist; R Rettenmeier; Gerd Scherer
Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1----q22.3 in a patient with tyrosinemia type II.
Human genetics 1987;77(4):352-8.
1987: U H Wiberg; Gerd Scherer
Evidence for the presence of testicular tissue and Sxs antigen in the absence of Y-derived sequences.
Development (Cambridge, England) 1987;101 Suppl():163-6.
1986: E Natt; F T Kao; R Rettenmeier; Gerd Scherer
Assignment of the human tyrosine aminotransferase gene to chromosome 16.
Human genetics 1986;72(3):225-8.