Scientific Commons: C. Larsson

The aim of this study was to characterize Swedish families with non-syndromic cleft lip and/or palate (NSCL/P) for mutations or other sequence variants in the interferon regulatory factor 6 (IRF6)...

Fracture strength of four-unit Y-TZP FPD cores designed with varying connector diameter. An in-vitro study. (2007)

Larsson, C, Vult Von Steyern, Per, Holm, L, Lövgren, N, Kokubo, Y

Reported clinical success rates of all-ceramic fixed partial dentures (FPDs) made of high-strength oxide ceramics range between 82.5% and 100%. The main cause of all-ceramic FPD failure is fracture...

All-ceramic two- to five-unit implant-supported reconstructions. A randomized, prospective clinical trial (2006)

Larsson, C, Vult Von Steyern, Per, Nilner, Krister, Sunzel, B

The purpose of this study was to evaluate the clinical performance of two to five-unit implant-supported all-ceramic reconstructions and to compare the results of two different all-ceramic systems,...

Menin interacts directly with the homeobox-containing protein Pem (2001)

Forsberg, L, Pannett, A A, Meyen, E, Piehl, F, Turner, J J, ...

The tumour suppressor gene causing multiple endocrine neoplasia type 1 (MEN1) encodes a 610 amino acid protein, menin. In order to identify menin-interacting proteins we used a yeast two-hybrid assay...

Expression of Escherichia coli otsA in a Saccharomyces cerevisiae tps1 mutant restores trehalose 6-phosphate levels and partly restores growth and fermentation with glucose and control of glucose influx into glycolysis (2000)

Larsson, C, Gustafsson, L, Ma, PS, ...

The TPS1 gene, encoding trehalose-6-phosphate synthase (TPS), exerts an essential control on the influx of glucose into glycolysis in the yeast Saccharomyces cerevisiae. The deletion of TPS1 causes...

Molecular characterization of human and murine C11orf5, a new member of the FAUNA gene cluster (2000)

Farnebo, F, Piehl, F, Merregaert, J, Larsson, C, ...

Laboratory for Molecular Oncology, Center for Human Genetics, University of Leuven & Flanders Interuniversity Institute for Biotechnology, Center for Human Genetics, KU Leuven, Herestraat 49, B-3000...

Phenotype and phenocopy: the relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1) (2000)

Burgess, JR, Nord, B, David, R, Greenaway, TM, Parameswaran, V, Larsson, C, ...

Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the meni gene in sporadic melanoma (2000)

Nord, B, Platz, A, Smoczynski, K, Kytola, S, Robertson, G, Calender, A, ...

Distinct deleted regions on chromosome segment 16q23-24 associated with metastases in prostate cancer. (1999)

LI, CD, Berx, Geert, LARSSON, C, AUER, G, ASPENBLAD, U, PAN, Y, ...

Localization and comparative toxicity of methylsulfonyl-2,5- and 2,6- dichlorobenzene in the olfactory mucosa of mice (1999)

Bahrami, F, Brittebo, EB, Bergman, A, Larsson, C, Brandt, I

A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1 (1998)

De Wit, M J, Simarro-Doorten, A Y, Roijers, J F, Van Herrewaarden, H M, Lips, C J, ...

In the process of identification of the multiple endocrine neoplasia type 1 gene, which was recently published, we isolated a novel gene in the 11q13 region. This gene (named ZFPL1, for zinc-finger...

Clinicopathologic Studies of Thymic Carcinoids in Multiple Endocrine Neoplasia Type 1 (1997)

Teh, BT, McArdle, J, Chan, SP, Menon, J, Hartley, L, Pullan, P, ...

Sporadic Primary Hyperparathyroidism in the Setting of Multiple Endocrine Neoplasia Type 1 (1997)

Teh, BT, McArdle, J, Parameswaran, V, David, R, Larsson, C, Shepherd, JJ

Multiple Endocrine Neoplasia (1996)

Teh, BT, Zedemius, J, Shepherd, JJ, Cameron, D, Larsson, C

Definition of the Minimal MEN1 Candidate Area Based on a 5-Mb Integrated Map of Proximal 11q13 (1996)

Courseaux, A, Grosgeorge, J, Gaudray, P, Pannett, AAJ, Forbes, SA, Williamson, C, ...

Responses of nitrate assimilation and N translocation in tomato (Lycopersicon esculentum Mill) to reduced ambient air humidity (1996)

Brewitz, E, Larsson, C, Larsson, M

Plant nutrition, dry matter gain and partitioning at the whole-plant level (1996)

McDonald, A, Ericsson, T, Larsson, C

Multiple Endocrine Neoplasia Type 1 - Clinical Syndrome to molecular genetics ome to Molecular Genetics (1995)

Teh, BT, Grimmond, S, Shepherd, JJ, Larsson, C, Hayward, N

Genetic mapping of the multiple endocrine neoplasia type 1 locus at 11q13 (1995)

Teh, BT, Cardinal, J, Shepherd, JJ, Hayward, N, Weber, G, Cameron, D, ...

Exclusion of the 13-kDa rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1 (1995)

Grimmond, S, Weber, G, Larsson, C, Walters, M, Teh, BT, Shepherd, JJ, ...

Activation of the Ig germ-line gamma 1 promoter. Involvement of C/enhancer-binding protein transcription factors and their possible interaction with an NF-IL-4 site (1994)

Lundgren, M., Larsson, C., Femino, Andrea, Xu, M., Stavnezer, Janet, Severinson, E.

Ig isotype switching in B lymphocytes is preceded by transcription of the corresponding unrearranged, or germ-line (GL), CH gene. The promoter of mouse GL C gamma 1 transcripts has been shown to be...

Assignment of the human FAU gene to a subregion of chromosome 11q13 (1993)

Weber, G, Nordenskjöld, M, Michiels, L, ...

The FAU gene is the cellular homologue of the fox sequence in the Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV). FAU (for FBR-MuSV associated ubiquitously expressed gene) encodes the ribosomal...

A polymorphism in the coding region of the vasopressin type 2 receptor (AVPR2) gene (1993)

Friedman, E, Carson, E, Larsson, C, DeMarco, L

BOOK REVIEWS (1993)

LARSSON, C.

An EcoRI RFLP at the human insulin-like growth factor binding protein 2 gene (IGFBP2) (1992)

Ehrenborg, E, Larsson, C

No improvement in a pilot study of tai chi exercise in rheumatoid arthritis

Uhlig, T, Larsson, C, Hjorth, A, Odegard, S, Kvien, T

Genetic studies of thymic carcinoids in multiple endocrine neoplasia type 1.

Teh, B T, Hayward, N K, Walters, M K, Shepherd, J J, Wilkinson, S, Nordenskjold, M, ...

Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one family

TEH, B, LINBLAD, K, NORD, B, KYTOLA, S, SCHALLING, M, LARSSON, C, ...

Association of a novel constitutional translocation t(1q;3q) with familial renal cell carcinoma

Kanayama, H., Lui, W., Takahashi, M., Naroda, T., Kedra, D., Wong, F. K., ...

Four cases of late onset clear cell renal cell carcinoma (RCC), a case of gastric cancer, and a case of exocrine pancreatic cancer were identified in a Japanese family. In order to elucidate the...

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome

WONG, F. K., KOILLINEN, H., RAUTIO, J., TEH, B. T., RANTA, R., KARSTEN, A., ...

Founder effect in multiple endocrine neoplasia type 1 (MEN 1) in Finland

KYTOLA, S, VILLABLANCA, A, EBELING, T, NORD, B, LARSSON, C, HOOG, A, ...

Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)

Villablanca, A, Calender, A, Forsberg, L, Hoog, A, Cheng, J, Petillo, D, ...

Frequent gain of the human telomerase gene TERC at 3q26 in cervical adenocarcinomas

Andersson, S, Wallin, K-L, Hellström, A-C, Morrison, L E, Hjerpe, A, Auer, G, ...

The level of genomic amplification of the human telomerase gene TERC, which maps to chromosome band 3q26, was determined in primary cervical adenocarcinomas. Interphase nuclei prepared from archival...

Comparative genomic hybridization reveals population-based genetic alterations in hepatoblastomas

Gray, S G, Kytölä, S, Matsunaga, T, Larsson, C, Ekström, T J

Hepatoblastoma is a malignant paediatric liver tumour. In order to approach the genetic background of this malignancy we have screened a panel of eighteen cases from Europe and Japan for chromosomal...

Gain of 17q in malignant fibrous histiocytoma is associated with a longer disease-free survival and a low risk of developing distant metastasis

Weng, W-H, Åhlén, J, Lui, W-O, Brosjö, O, Pang, S-T, Von Rosen, A, ...

Association between low concentrations of antibodies to protein α and Rib and invasive neonatal group B streptococcal infection

Larsson, C, Lindroth, M, Nordin, P, Stålhammar‐Carlemalm, M, Lindahl, G, Krantz, I

C. Larsson

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