Publications by authors named "Osinga Jan"

Claim this Profile
A
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome.
Mark Drost, Yvonne Tiersma, Bryony A Thompson, Jane H Frederiksen, Guido Keijzers, Jan Osinga

Genet Med· July 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
MicroRNA High Throughput Loss-of-Function Screening Reveals an Oncogenic Role for miR-21-5p in Hodgkin Lymphoma.
Ye Yuan, Fubiao Niu, Ilja M Nolte, Jasper Koerts, Debora de Jong, Jan Osinga, Arjan Diepstra

Cell Physiol Biochem· September 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease.
Yunia Sribudiani, Rajendra K Chauhan, Maria M Alves, Lucy Petrova, Erwin Brosens, Jan Osinga

Gastroenterology· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Functional Studies on Primary Tubular Epithelial Cells Indicate a Tumor Suppressor Role of SETD2 in Clear Cell Renal Cell Carcinoma.
Jun Li, Joost Kluiver, Jan Osinga, Helga Westers, Maaike B van Werkhoven

Neoplasia· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
New target genes in endometrial tumors show a role for the estrogen-receptor pathway in microsatellite-unstable cancers.
Ana M Ferreira, Iina Tuominen, Sónia Sousa, Frans Gerbens, Krista van Dijk-Bos, Jan Osinga

Hum Mutat· December 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Relation between genotype and left-ventricular dilatation in patients with Marfan syndrome.
Jan J J Aalberts, J Peter van Tintelen, Lilian J Meijboom, Annette Polko, Jan D H Jongbloed, Jan Osinga, Janneke Timmermans

Gene· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Targeted exome sequencing in clear cell renal cell carcinoma tumors suggests aberrant chromatin regulation as a crucial step in ccRCC development.
Gerben Duns, Robert M W Hofstra, Jantine G Sietzema, Harry Hollema, Inge van Duivenbode, Osinga Jan

Hum Mutat· July 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The effects of four different tyrosine kinase inhibitors on medullary and papillary thyroid cancer cells.
Hans H G Verbeek, Maria M Alves, Jan-Willem B de Groot, Jan Osinga, John T M Plukker

J Clin Endocrinol Metab· June 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Variants in RET associated with Hirschsprung's disease affect binding of transcription factors and gene expression.
Yunia Sribudiani, Marco Metzger, Jan Osinga, Amanda Rey, Alan J Burns

Gastroenterology· February 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in SCG10 are not involved in Hirschsprung disease.
Maria M M Alves, Jan Osinga, Joke B G M Verheij, Marco Metzger, Bart J L Eggen

PLoS One· December 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
K
KBP interacts with SCG10, linking Goldberg-Shprintzen syndrome to microtubule dynamics and neuronal differentiation.
Maria M Alves, Grzegorz Burzynski, Jean-Marie Delalande, Jan Osinga, Annemieke van der Goot

Hum Mol Genet· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Histone methyltransferase gene SETD2 is a novel tumor suppressor gene in clear cell renal cell carcinoma.
Gerben Duns, Eva van den Berg, Inge van Duivenbode, Jan Osinga, Harry Hollema

Cancer Res· June 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C gene.
J Peter van Tintelen, Rene A Tio, Wilhelmina S Kerstjens-Frederikse, Jop H van Berlo, Ludolf G Boven, Jan Osinga

J Am Coll Cardiol· June 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
MUTYH and the mismatch repair system: partners in crime?
Renée C Niessen, Rolf H Sijmons, J Ou, Sandra G M Olthof, Jan Osinga, Marjan M Weiss, Jan H Kleibeuker

Hum Genet· March 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systems.
Alice S Brooks, Aida M Bertoli-Avella, Grzegorz M Burzynski, Guido J Breedveld, Jan Osinga, Jane A Hurst

Am J Hum Genet· July 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identifying candidate Hirschsprung disease-associated RET variants.
Grzegorz M Burzynski, Ilja M Nolte, Agnes Bronda, Krista K Bos, Jan Osinga

Am J Hum Genet· May 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
RET-familial medullary thyroid carcinoma mutants Y791F and S891A activate a Src/JAK/STAT3 pathway, independent of glial cell line-derived neurotrophic factor.
Ivan Plaza Menacho, Roelof Koster, Almer M van der Sloot, Wim J Quax, Jan Osinga

Cancer Res· March 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2.
Grzegorz M Burzynski, Ilja M Nolte, Jan Osinga, Isabella Ceccherini, Bas Twigt

Eur J Hum Genet· August 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung disease.
Paola Griseri, Barbara Pesce, Giovanna Patrone, Jan Osinga, Francesca Puppo

Am J Hum Genet· October 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
ABCD syndrome is caused by a homozygous mutation in the EDNRB gene.
Joke B G M Verheij, Jürgen Kunze, Jan Osinga, Anthonie J van Essen, Robert M W Hofstra

Am J Med Genet· March 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis