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1

Human homologue of the murinebare patches/striated gene is not mutated in incontinentia pigmenti type 2

Aradhya, Swaroop, Nelson, David L., Heiss, Nina S., Poustka, Annemarie, Woffendin, Hayley, Kenwrick, Susan, Esposito, Teresa, Ciccodicola, Alfredo, Bardaro, Tiziana, D'Urso, Michele, Smahi, Asmae, Mun

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 477 KB

english, 2000

2

Biodegradable β-Tri-Calciumphosphate/hydroxyethyl methacrylate enhanced three component bone adhesive demonstrates biocompatibility without evidence of systemic toxicity in a rabbit model

Natali B. Bauer, Nina Brinke, Christian Heiss, Agnes B. Skorupa, Fabian Peters, Ralf Kraus, Reinhard Schnettler, Andreas Moritz

Journal:

Journal of Biomedical Materials Research Part B: Applied Biomaterials

Year:

2009

Language:

english

File:

PDF, 449 KB

english, 2009

3

10.1038/35013114

Kenwrick, S. J., The International Incontinentia Pigmenti (IP) Consortium,, France,, Smahi, Asmae, Courtois, G., Vabres, P., Yamaoka, S., Heuertz, S., Munnich, A., Israël, A., Germany,, Heiss, Nina

Journal:

Year:

2000

Language:

english

File:

PDF, 403 KB

english, 2000

4

10.1038/35013127

Kenwrick, S. J., The International Incontinentia Pigmenti (IP) Consortium,, France,, Smahi, Asmae, Courtois, G., Vabres, P., Yamaoka, S., Heuertz, S., Munnich, A., Israël, A., Germany,, Heiss, Nina

Journal:

Year:

2000

Language:

english

File:

PDF, 180 KB

english, 2000

5

10.1038/35013122

Kenwrick, S. J., The International Incontinentia Pigmenti (IP) Consortium,, France,, Smahi, Asmae, Courtois, G., Vabres, P., Yamaoka, S., Heuertz, S., Munnich, A., Israël, A., Germany,, Heiss, Nina

Journal:

Year:

2000

Language:

english

File:

PDF, 239 KB

english, 2000

6

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions

Heiss, Nina S., Knight, Stuart W., Vulliamy, Tom J., Klauck, Sabine M., Wiemann, Stefan, Mason, Philip J., Poustka, Annemarie, Dokal, Inderjeet

Journal:

Nature Genetics

Year:

1998

File:

PDF, 1.32 MB

1998

7

Amplification and expression of the TGF-α, EGF receptor and c-mycgenes in four human oesophageal squamous cell carcinoma lines

Gregory J. Jones, Nina S. Heiss, Robin B. Veale, Alan L. Thornley

Journal:

Bioscience Reports

Year:

1993

Language:

english

File:

PDF, 785 KB

english, 1993

8

A 900-kb Cosmid Contig and 10 New Transcripts within the Candidate Region for Myotubular Myopathy (MTM1)

Petra Kioschis, Ute C. Rogner, Elke Pick, Sabine M. Klauck, Nina Heiss, Renate Siebenhaar, Bernhard Korn, Johannes F. Coy, Jocelyn Laporte, Sabina Liechti-Gallati, Annemarie Poustka

Journal:

Year:

1996

Language:

english

File:

PDF, 230 KB

english, 1996

9

Genomic Structure of a Novel LIM Domain Gene (ZNF185) in Xq28 and Comparisons with the Orthologous Murine Transcript

Nina S Heiss, Gernot Gloeckner, Dietmar Bächner, Petra Kioschis, Sabine M Klauck, Bernd Hinzmann, André Rosenthal, Gail E Herman, Annemarie Poustka

Journal:

Year:

1997

Language:

english

File:

PDF, 1.58 MB

english, 1997

10

Genomic Structure of a Novel Chloride Channel Gene, CLIC2, in Xq28

Nina S. Heiss, Annemarie Poustka

Journal:

Year:

1997

Language:

english

File:

PDF, 111 KB

english, 1997

11

Genomic Organization of a 225-kb Region in Xq28 Containing the Gene for X-Linked Myotubular Myopathy (MTM1) and a Related Gene (MTMR1)

Petra Kioschis, Stefan Wiemann, Nina S. Heiss, Fiona Francis, Carmen Götz, Annemarie Poustka, Stefan Taudien, Matthias Platzer, Thomas Wiehe, Georg Beckmann, Jacqueline Weber, Gabriele Nordsiek, André

Journal:

Year:

1998

Language:

english

File:

PDF, 910 KB

english, 1998

12

Transcription Mapping in a Medulloblastoma Breakpoint Interval and Smith–Magenis Syndrome Candidate Region: Identification of 53 Transcriptional Units and New Candidate Genes

Peter Seranski, Nina S. Heiss, Sophie Dhorne-Pollet, Uwe Radelof, Bernhard Korn, Steffen Hennig, Esther Backes, Sabine Schmidt, Stefan Wiemann, Charles E. Schwarz, Hans Lehrach, Annemarie Poustka

Journal:

Year:

1999

Language:

english

File:

PDF, 191 KB

english, 1999

13

Gene Structure and Expression of the Mouse Dyskeratosis Congenita Gene, Dkc1

Nina S. Heiss, Dietmar Bächner, Rüdiger Salowsky, Anja Kolb, Petra Kioschis, Annemarie Poustka

Journal:

Year:

2000

Language:

english

File:

PDF, 908 KB

english, 2000

14

Physical and Genetic Characterization Reveals a Pseudogene, an Evolutionary Junction, and Unstable Loci in Distal Xq28

Swaroop Aradhya, Hayley Woffendin, Penelope Bonnen, Nina S. Heiss, Takanori Yamagata, Teresa Esposito, Tiziana Bardaro, Annemarie Poustka, Michele D'Urso, Sue Kenwrick, David L. Nelson

Journal:

Year:

2002

Language:

english

File:

PDF, 423 KB

english, 2002

15

RAI1 is a novel polyglutamine encoding gene that is deleted in Smith–Magenis syndrome patients

Peter Seranski, Céline Hoff, Uwe Radelof, Steffen Hennig, Richard Reinhardt, Charles E Schwartz, Nina S Heiss, Annemarie Poustka

Journal:

Year:

2001

Language:

english

File:

PDF, 840 KB

english, 2001

16

Basal transcription activity of the dyskeratosis congenita gene is mediated by Sp1 and Sp3 and a patient mutation in a Sp1 binding site is associated with decreased promoter activity

Rüdiger Salowsky, Nina S Heiss, Axel Benner, Rainer Wittig, Annemarie Poustka

Journal:

Year:

2002

Language:

english

File:

PDF, 735 KB

english, 2002

17

Overlap of dyskeratosis congenita with the Hoyeraal-Hreidarsson syndrome

Reza Yaghmai, Arash Kimyai-Asadi, Karoline Rostamiani, Nina S Heiss, Annemarie Poustka, Wafaa Eyaid, Joann Bodurtha, Hossein C Nousari, Ada Hamosh, Aida Metzenberg

Journal:

The Journal of Pediatrics

Year:

2000

Language:

english

File:

PDF, 69 KB

english, 2000

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