Transcriptional hallmarks of noonan syndrome and noonan‐like syndrome with loose anagen hair-Reference-Cited by-同舟云学术

Transcriptional hallmarks of noonan syndrome and noonan‐like syndrome with loose anagen hair

Published:2012-02-14 Issue:4 Volume:33 Page:703-709
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Ferrero Giovanni Battista¹,Picco Gabriele²³,Baldassarre Giuseppina¹,Flex Elisabetta⁴,Isella Claudio²³,Cantarella Daniela²³,Corà Davide⁵,Chiesa Nicoletta¹,Crescenzio Nicoletta¹,Timeus Fabio¹,Merla Giuseppe⁶,Mazzanti Laura⁷,Zampino Giuseppe⁸,Rossi Cesare⁹,Silengo Margherita¹,Tartaglia Marco⁴,Medico Enzo²³

Affiliation:

1. Department of Pediatrics, University of Torino Medical School, Torino, Italy

2. Department of Oncological Sciences, University of Torino Medical School, Torino, Italy

3. Laboratory of Oncogenomics, Institute for Cancer Research and Treatment, Candiolo (Torino), Italy

4. Dipartimento di Ematologia, Oncologia e Medicina Molecolare, Istituto Superiore di Sanità, Roma, Italy

5. Laboratory of Systems Biology, Institute for Cancer Research and Treatment (IRCC), 10060 Candiolo (Torino), Italy

6. Medical Genetics Unit, IRCCS ‘Casa Sollievo della Sofferenza’, S. Giovanni Rotondo, Italy

7. Dipartimento di Pediatria, Università degli Studi di Bologna, Bologna, Italy

8. Istituto di Clinica Pediatrica, Università Cattolica del Sacro Cuore, Roma, Italy

9. UO Genetica Medica, Policlinico S.Orsola‐Malpighi, Bologna, Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.22026

Reference49 articles.

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4. MAPK and JNK transduction pathways can phosphorylate Sp1 to activate the uPA minimal promoter element and endogenous gene transcription

5. Genes2Networks: connecting lists of gene symbols using mammalian protein interactions databases

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