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3D follow‐up study of facial asymmetry after developmental dysplasia of the hip

Orthodontics & craniofacial research, 2018-08, Vol.21 (3), p.146-152

2018

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80P Oncolytic adenovirus type 3 coding for CD40L facilitates dendritic cell therapy of prostate cancer in humanized mice and patient samples

Annals of oncology, 2020-12, Vol.31, p.S1449-S1450

2020

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Analysis of 11q21-24 loss of heterozygosity candidate target genes in breast cancer: Indications of TSLC1 promoter hypermethylation

Genes chromosomes & cancer, 2002-08, Vol.34 (4), p.384-389

2002

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The androgen receptor depends on ligand‐binding domain dimerization for transcriptional activation

EMBO reports, 2021-12, Vol.22 (12), p.e52764-n/a

2021

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Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer

Journal of endocrinological investigation, 2009-05, Vol.32 (5), p.426-429

2009

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ATM mutations in Finnish breast cancer patients

Journal of medical genetics, 2002-03, Vol.39 (3), p.192-196

2002

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Biallelic Inactivation of Fumarate Hydratase ( FH) Occurs in Nonsyndromic Uterine Leiomyomas but Is Rare in Other Tumors

The American journal of pathology, 2004, Vol.164 (1), p.17-22

2004

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Chromosome 11q22.3-q25 LOH in Ovarian Cancer: Association with a More Aggressive Disease Course and Involved Subregions

Gynecologic oncology, 1998-11, Vol.71 (2), p.299-304

1998

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Orthodontics & craniofacial research, 2018-08, Vol.21 (3)

2018

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Distal Biceps Tendon Rupture Surgery: Changing Incidence in Finnish and Swedish Men Between 1997 and 2016

The Journal of hand surgery (American ed.), 2020-11, Vol.45 (11), p.1022-1028

2020

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DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

Human molecular genetics, 2001-12, Vol.10 (26), p.3001-3007

2001

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Do Treatment Policies for Proximal Humerus Fractures Differ among Three Nordic Countries and Estonia? Results of a Survey Study

Scandinavian journal of surgery, 2016-09, Vol.105 (3), p.186-190

2016

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E-cadherin is not frequently mutated in hereditary gastric cancer

Journal of medical genetics, 2001, Vol.38 (1), p.49-52

2001

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E-cadherinis not frequently mutated in hereditary gastric cancer

Journal of medical genetics, 2001-01, Vol.38 (1), p.49-52

2001

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Epidemiology of proximal humerus fractures

Archives of osteoporosis, 2015, Vol.10 (1), p.209-209, Article 2

2015

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European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables

British Journal of Cancer, 1999-05, Vol.80 (5-6), p.879-882

1999

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European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables. Breast Cancer Somatic Genetics Consortium

British journal of cancer, 1999-05, Vol.80 (5-6), p.879-882

1999

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Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families

American journal of human genetics, 1998-06, Vol.62 (6), p.1544-1548

1998

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Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology

The American journal of pathology, 2001-09, Vol.159 (3), p.825-829

2001

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Frequent loss of SMAD4/DPC4 protein in colorectal cancers

Molecular pathology, 2002-12, Vol.55 (6), p.385-388

2002

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Frequent loss of SMAD4/DPC4 protein in colorectal cancers

Gut, 2002-07, Vol.51 (1), p.56-59

2002

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Frequent loss of SMAD4/DPCA protein in colorectal cancers

Molecular pathology, 2002-12, Vol.55 (6), p.385

2002

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Germ Line Insertions of Moloney Murine Leukemia Virus in the TLL Mouse Causes Site-specific Differences in Lymphoma/Leukemia Frequency and Tumor Immunophenotype

Anticancer research, 2006-07, Vol.26 (4B), p.2873-2878

2006

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Germ-Line TP53 Mutations in Finnish Cancer Families Exhibiting Features of the Li-Fraumeni Syndrome and Negative for BRCA1 and BRCA2

Cancer genetics and cytogenetics, 1999-07, Vol.112 (1), p.9-14

1999

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Germline and Somatic Mutation Analysis of MLH3 in MSI-Positive Colorectal Cancer

The American journal of pathology, 2000-08, Vol.157 (2), p.347-352

2000

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3D follow‐up study of facial asymmetry after developmental dysplasia of the hip

80P Oncolytic adenovirus type 3 coding for CD40L facilitates dendritic cell therapy of prostate cancer in humanized mice and patient samples

Analysis of 11q21-24 loss of heterozygosity candidate target genes in breast cancer: Indications of TSLC1 promoter hypermethylation

The androgen receptor depends on ligand‐binding domain dimerization for transcriptional activation

Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer

ATM mutations in Finnish breast cancer patients

Biallelic Inactivation of Fumarate Hydratase ( FH) Occurs in Nonsyndromic Uterine Leiomyomas but Is Rare in Other Tumors

Chromosome 11q22.3-q25 LOH in Ovarian Cancer: Association with a More Aggressive Disease Course and Involved Subregions

Cover Image

Distal Biceps Tendon Rupture Surgery: Changing Incidence in Finnish and Swedish Men Between 1997 and 2016

DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

Do Treatment Policies for Proximal Humerus Fractures Differ among Three Nordic Countries and Estonia? Results of a Survey Study

E-cadherin is not frequently mutated in hereditary gastric cancer

E-cadherinis not frequently mutated in hereditary gastric cancer

Epidemiology of proximal humerus fractures

European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables

European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables. Breast Cancer Somatic Genetics Consortium

Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families

Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology

Frequent loss of SMAD4/DPC4 protein in colorectal cancers

Frequent loss of SMAD4/DPC4 protein in colorectal cancers

Frequent loss of SMAD4/DPCA protein in colorectal cancers

Germ Line Insertions of Moloney Murine Leukemia Virus in the TLL Mouse Causes Site-specific Differences in Lymphoma/Leukemia Frequency and Tumor Immunophenotype

Germ-Line TP53 Mutations in Finnish Cancer Families Exhibiting Features of the Li-Fraumeni Syndrome and Negative for BRCA1 and BRCA2

Germline and Somatic Mutation Analysis of MLH3 in MSI-Positive Colorectal Cancer

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