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Publications by Birgitta Kranz

Clinical and Molecular Characterization of Patients With Heterozygous Mutations in Wilms Tumor Suppressor Gene 1

Clinical Journal of the American Society of Nephrology

Transplantation

Intensive Care Medicine

English

Related publications

Region-Specific Astrogliosis in Brains of Mice Heterozygous for Mutations in the Neurofibromatosis Type 1 (Nf1) Tumor Suppressor

Developmental Biology

Molecular Biology

English

Identification of Novel Wilms' Tumor Suppressor Gene Target Genes Implicated in Kidney Development

Journal of Biological Chemistry

Molecular Biology

English

Clinical Utility of Wilms' Tumor 1 Monitoring in Patients With Myeloid Malignancy and Prior Allogeneic Hematopoietic Stem Cell Transplantation

Biology of Blood and Marrow Transplantation

Transplantation

English

Reduced Mitochondrial DNA Content and Heterozygous Nuclear Gene Mutations in Patients With Acute Liver Failure

Journal of Pediatric Gastroenterology and Nutrition

Gastroenterology

English

Molecular Mechanisms of Functional Rescue Mediated by P53 Tumor Suppressor Mutations

Biophysical Chemistry

Organic Chemistry

English

Molecular and Phenotypic Abnormalities in Individuals With Germline Heterozygous PTEN Mutations and Autism

Molecular Psychiatry

Molecular Neuroscience

Molecular Biology

English

Characterization of the Novel Tumor-Suppressor Gene CCDC67 in Papillary Thyroid Carcinoma

English

Congenital Dyserythropoietic Anemia Type 1: A Case With Novel Compound Heterozygous Mutations in the C15orf41 Gene

American Journal of Hematology

English

Comprehensive Molecular and Clinical Characterization of Asian Melanoma Patients Treated With Anti-Pd-1 Antibody

Cancer Research

English