Meinrad Busslinger - Publications

Publications (23)

ECB-PERS-4284

Publications By Meinrad Busslinger

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The characterization of novel Pax genes of the sea urchin and Drosophila reveal an ancient evolutionary origin of the Pax2/5/8 subfamily., Czerny T, Bouchard M, Kozmik Z, Busslinger M., Mech Dev. October 1, 1997; 67 (2): 179-92.
Isolation and amino acid sequence analysis reveal an ancient evolutionary origin of the cleavage stage (CS) histones of the sea urchin., Brandt WF, Schwager SU, Rodrigues JA, Busslinger M., Eur J Biochem. August 1, 1997; 247 (3): 784-91.
The five cleavage-stage (CS) histones of the sea urchin are encoded by a maternally expressed family of replacement histone genes: functional equivalence of the CS H1 and frog H1M (B4) proteins., Mandl B, Brandt WF, Superti-Furga G, Graninger PG, Birnstiel ML, Busslinger M., Mol Cell Biol. March 1, 1997; 17 (3): 1189-200.
C-terminal activating and inhibitory domains determine the transactivation potential of BSAP (Pax-5), Pax-2 and Pax-8., Dörfler P, Busslinger M., EMBO J. April 15, 1996; 15 (8): 1971-82.
DNA-binding and transactivation properties of Pax-6: three amino acids in the paired domain are responsible for the different sequence recognition of Pax-6 and BSAP (Pax-5)., Czerny T, Busslinger M., Mol Cell Biol. May 1, 1995; 15 (5): 2858-71.
The transcription factor BSAP (NF-HB) is essential for immunoglobulin germ-line epsilon transcription., Liao F, Birshtein BK, Busslinger M, Rothman P., J Immunol. March 15, 1994; 152 (6): 2904-11.
A novel B-cell lineage-specific transcription factor present at early but not late stages of differentiation., Barberis A, Widenhorn K, Vitelli L, Busslinger M., Genes Dev. May 1, 1990; 4 (5): 849-59.
The testis-specific octamer-binding protein of the sea urchin has a molecular weight of 85 kDa., Barberis A, Superti-Furga G, Busslinger M., Nucleic Acids Res. September 12, 1989; 17 (17): 7114.
Developmental and tissue-specific regulation of a novel transcription factor of the sea urchin., Barberis A, Superti-Furga G, Vitelli L, Kemler I, Busslinger M., Genes Dev. May 1, 1989; 3 (5): 663-75.
The protein CDP, but not CP1, footprints on the CCAAT region of the gamma-globin gene in unfractionated B-cell extracts., Superti-Furga G, Barberis A, Schreiber E, Busslinger M., Biochim Biophys Acta. March 1, 1989; 1007 (2): 237-42.
In vivo and in vitro expression of U7 snRNA genes: cis- and trans-acting elements required for RNA polymerase II-directed transcription., Southgate C, Busslinger M., EMBO J. February 1, 1989; 8 (2): 539-49.
The -117 mutation in Greek HPFH affects the binding of three nuclear factors to the CCAAT region of the gamma-globin gene., Superti-Furga G, Barberis A, Schaffner G, Busslinger M., EMBO J. October 1, 1988; 7 (10): 3099-107.
Promoter of a somatic histone H2B gene of the sea urchin., Cosson J, Kemler I, Tanno S, Busslinger M., Nucleic Acids Res. May 11, 1988; 16 (9): 4175.
Developmental regulation of micro-injected histone genes in sea urchin embryos., Vitelli L, Kemler I, Lauber B, Birnstiel ML, Busslinger M., Dev Biol. May 1, 1988; 127 (1): 54-63.
Mutually exclusive interaction of the CCAAT-binding factor and of a displacement protein with overlapping sequences of a histone gene promoter., Barberis A, Superti-Furga G, Busslinger M., Cell. July 31, 1987; 50 (3): 347-59.
Characterization of two nonallelic pairs of late histone H2A and H2B genes of the sea urchin: differential regulation in the embryo and tissue-specific expression in the adult., Kemler I, Busslinger M., Mol Cell Biol. November 1, 1986; 6 (11): 3746-54.
Synthesis of sperm and late histone cDNAs of the sea urchin with a primer complementary to the conserved 3'' terminal palindrome: evidence for tissue-specific and more general histone gene variants., Busslinger M, Barberis A., Proc Natl Acad Sci U S A. September 1, 1985; 82 (17): 5676-80.
Regulation of histone gene expression., Busslinger M, Schümperli D, Birnstiel ML., Cold Spring Harb Symp Quant Biol. January 1, 1985; 50 665-70.
The cDNA sequences of the sea urchin U7 small nuclear RNA suggest specific contacts between histone mRNA precursor and U7 RNA during RNA processing., Strub K, Galli G, Busslinger M, Birnstiel ML., EMBO J. December 1, 1984; 3 (12): 2801-7.
An unusual evolutionary behaviour of a sea urchin histone gene cluster., Busslinger M, Rusconi S, Birnstiel ML., EMBO J. January 1, 1982; 1 (1): 27-33.
Ubiquitous and gene-specific regulatory 5'' sequences in a sea urchin histone DNA clone coding for histone protein variants., Busslinger M, Portmann R, Irminger JC, Birnstiel ML., Nucleic Acids Res. March 11, 1980; 8 (5): 957-77.
A regulatory sequence near the 3'' end of sea urchin histone genes., Busslinger M, Portmann R, Birnsteil ML., Nucleic Acids Res. July 11, 1979; 6 (9): 2997-3008.
Aspects of the regulation of histone genes., Birnstiel ML, Kressmann A, Schaffner W, Portmann R, Busslinger M., Philos Trans R Soc Lond B Biol Sci. May 11, 1978; 283 (997): 319-24.

The characterization of novel Pax genes of the sea urchin and Drosophila reveal an ancient evolutionary origin of the Pax2/5/8 subfamily., Czerny T, Bouchard M, Kozmik Z, Busslinger M., Mech Dev. October 1, 1997; 67 (2): 179-92.

Isolation and amino acid sequence analysis reveal an ancient evolutionary origin of the cleavage stage (CS) histones of the sea urchin., Brandt WF, Schwager SU, Rodrigues JA, Busslinger M., Eur J Biochem. August 1, 1997; 247 (3): 784-91.

The five cleavage-stage (CS) histones of the sea urchin are encoded by a maternally expressed family of replacement histone genes: functional equivalence of the CS H1 and frog H1M (B4) proteins., Mandl B, Brandt WF, Superti-Furga G, Graninger PG, Birnstiel ML, Busslinger M., Mol Cell Biol. March 1, 1997; 17 (3): 1189-200.

C-terminal activating and inhibitory domains determine the transactivation potential of BSAP (Pax-5), Pax-2 and Pax-8., Dörfler P, Busslinger M., EMBO J. April 15, 1996; 15 (8): 1971-82.

DNA-binding and transactivation properties of Pax-6: three amino acids in the paired domain are responsible for the different sequence recognition of Pax-6 and BSAP (Pax-5)., Czerny T, Busslinger M., Mol Cell Biol. May 1, 1995; 15 (5): 2858-71.

The transcription factor BSAP (NF-HB) is essential for immunoglobulin germ-line epsilon transcription., Liao F, Birshtein BK, Busslinger M, Rothman P., J Immunol. March 15, 1994; 152 (6): 2904-11.

A novel B-cell lineage-specific transcription factor present at early but not late stages of differentiation., Barberis A, Widenhorn K, Vitelli L, Busslinger M., Genes Dev. May 1, 1990; 4 (5): 849-59.

The testis-specific octamer-binding protein of the sea urchin has a molecular weight of 85 kDa., Barberis A, Superti-Furga G, Busslinger M., Nucleic Acids Res. September 12, 1989; 17 (17): 7114.

Developmental and tissue-specific regulation of a novel transcription factor of the sea urchin., Barberis A, Superti-Furga G, Vitelli L, Kemler I, Busslinger M., Genes Dev. May 1, 1989; 3 (5): 663-75.

The protein CDP, but not CP1, footprints on the CCAAT region of the gamma-globin gene in unfractionated B-cell extracts., Superti-Furga G, Barberis A, Schreiber E, Busslinger M., Biochim Biophys Acta. March 1, 1989; 1007 (2): 237-42.

In vivo and in vitro expression of U7 snRNA genes: cis- and trans-acting elements required for RNA polymerase II-directed transcription., Southgate C, Busslinger M., EMBO J. February 1, 1989; 8 (2): 539-49.

The -117 mutation in Greek HPFH affects the binding of three nuclear factors to the CCAAT region of the gamma-globin gene., Superti-Furga G, Barberis A, Schaffner G, Busslinger M., EMBO J. October 1, 1988; 7 (10): 3099-107.

Promoter of a somatic histone H2B gene of the sea urchin., Cosson J, Kemler I, Tanno S, Busslinger M., Nucleic Acids Res. May 11, 1988; 16 (9): 4175.

Developmental regulation of micro-injected histone genes in sea urchin embryos., Vitelli L, Kemler I, Lauber B, Birnstiel ML, Busslinger M., Dev Biol. May 1, 1988; 127 (1): 54-63.

Mutually exclusive interaction of the CCAAT-binding factor and of a displacement protein with overlapping sequences of a histone gene promoter., Barberis A, Superti-Furga G, Busslinger M., Cell. July 31, 1987; 50 (3): 347-59.

Characterization of two nonallelic pairs of late histone H2A and H2B genes of the sea urchin: differential regulation in the embryo and tissue-specific expression in the adult., Kemler I, Busslinger M., Mol Cell Biol. November 1, 1986; 6 (11): 3746-54.

Synthesis of sperm and late histone cDNAs of the sea urchin with a primer complementary to the conserved 3'' terminal palindrome: evidence for tissue-specific and more general histone gene variants., Busslinger M, Barberis A., Proc Natl Acad Sci U S A. September 1, 1985; 82 (17): 5676-80.

Regulation of histone gene expression., Busslinger M, Schümperli D, Birnstiel ML., Cold Spring Harb Symp Quant Biol. January 1, 1985; 50 665-70.

The cDNA sequences of the sea urchin U7 small nuclear RNA suggest specific contacts between histone mRNA precursor and U7 RNA during RNA processing., Strub K, Galli G, Busslinger M, Birnstiel ML., EMBO J. December 1, 1984; 3 (12): 2801-7.

An unusual evolutionary behaviour of a sea urchin histone gene cluster., Busslinger M, Rusconi S, Birnstiel ML., EMBO J. January 1, 1982; 1 (1): 27-33.

Ubiquitous and gene-specific regulatory 5'' sequences in a sea urchin histone DNA clone coding for histone protein variants., Busslinger M, Portmann R, Irminger JC, Birnstiel ML., Nucleic Acids Res. March 11, 1980; 8 (5): 957-77.

A regulatory sequence near the 3'' end of sea urchin histone genes., Busslinger M, Portmann R, Birnsteil ML., Nucleic Acids Res. July 11, 1979; 6 (9): 2997-3008.

Aspects of the regulation of histone genes., Birnstiel ML, Kressmann A, Schaffner W, Portmann R, Busslinger M., Philos Trans R Soc Lond B Biol Sci. May 11, 1978; 283 (997): 319-24.

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