Schedl, Andreas

The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6

Akiyama, H., Chaboissier, M.-C., Martin, J. F., Schedl, A., & de Crombrugghe, B. (2002) · Genes & Development

Osteoarthritis Treatment and MechanismsDevelopmental Biology and Gene Regulation

Cited by 1,721

The Sox9 transcription factor determines glial fate choice in the developing spinal cord

Stolt, C. C., Lommes, P., Sock, E., Chaboissier, M.-C., Schedl, A., & Wegner, M. (2003) · Genes & Development

Neurogenesis and neuroplasticity mechanismsDevelopmental Biology and Gene Regulation

Cited by 636

Visceral and subcutaneous fat have different origins and evidence supports a mesothelial source

Chau, Y.-Y., Bandiera, R., Serrels, A., Martínez-Estrada, O. M., Qing, W., Lee, M., Slight, J., Thornburn, A., Berry, R., McHaffie, S., et al. (2014) · Nature Cell Biology

Adipose Tissue and MetabolismAdipokines, Inflammation, and Metabolic Diseases

Cited by 518

The transcriptional control of trunk neural crest induction, survival, and delamination

Cheung, M., Chaboissier, M.-C., Mynett, A., Hirst, E., Schedl, A., & Briscoe, J. (2005) · Developmental Cell

Developmental Biology and Gene RegulationNeurogenesis and neuroplasticity mechanisms

Cited by 427

Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease

Joutel, A., Monet-Leprêtre, M., Gosele, C., Baron-Menguy, C., Hammes, A., Schmidt, S., Lemaire-Carrette, B., Domenga, V., Schedl, A., Lacombe, P., et al. (2010) · Journal of Clinical Investigation

Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments

Cited by 379

Essential role of Sox9 in the pathway that controls formation of cardiac valves and septa

Akiyama, H., Chaboissier, M.-C., Behringer, R. R., Rowitch, D. H., Schedl, A., Epstein, J. A., & de Crombrugghe, B. (2004) · Proceedings of the National Academy of Sciences

Congenital heart defects researchDevelopmental Biology and Gene Regulation

Cited by 265

The Angiocrine Factor Rspondin3 Is a Key Determinant of Liver Zonation

Rocha, A. S., Vidal, V., Mertz, M., Kendall, T. J., Charlet, A., Okamoto, H., & Schedl, A. (2015) · Cell Reports

Liver physiology and pathologyWnt/β-catenin signaling in development and cancer

Cited by 194

PKA inhibits WNT signalling in adrenal cortex zonation and prevents malignant tumour development

Drelon, C., Berthon, A., Sahut-Barnola, I., Mathieu, M., Dumontet, T., Rodriguez, S., Batisse-Lignier, M., Tabbal, H., Tauveron, I., Lefrançois-Martinez, A.-M., et al. (2016) · Nature Communications

Wnt/β-catenin signaling in development and cancerAdrenal and Paraganglionic Tumors

Cited by 128

Deficiency of an enzyme of tyrosine metabolism underlies altered gene expression in newborn liver of lethal albino mice.

Ruppert, S., Kelsey, G., Schedl, A., Schmid, E., Thies, E., & Schütz, G. (1992) · Genes & Development

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 95

Molecular mapping of albino deletions associated with early embryonic lethality in the mouse

Niswander, L., Kelsey^, G., Schedl, A., Ruppert, S., Sharan, S. K., Holdener-Kenny, B., Rinchik, E. M., Edström, J.-E., & Magnuson, T. (1991) · Genomics

Genomic variations and chromosomal abnormalitiesDevelopmental Biology and Gene Regulation

Cited by 28

Physical mapping of the albino-deletion complex in the mouse to localize alf/hsdr-1, a locus required for neonatal survival

Kelsey, G., Schedl, A., Ruppert, S., Niswander, L., Magnuson, T., Klebig, M. L., Rinchik, E. M., & Schütz, G. (1992) · Genomics

Genomic variations and chromosomal abnormalitiesGenetic Mapping and Diversity in Plants and Animals

Cited by 28

New Horizons: Novel Adrenal Regenerative Therapies

Bornstein, S. R., Malyukov, M., Heller, C., Ziegler, C. G., Ruiz-Babot, G., Schedl, A., Ludwig, B., & Steenblock, C. (2020) · The Journal of Clinical Endocrinology & Metabolism

Adrenal Hormones and DisordersPancreatic function and diabetes

Cited by 23

Chromosome jumping from flanking markers defines the minimal region for alf/hsdr-1 within the albino-deletion complex

Schedl, A., Ruppert, S., Kelsey, G., Thies, E., Niswander, L., Magnuson, T., Klebig, M. L., Rinchik, E. M., & Schütz, G. (1992) · Genomics

Genomic variations and chromosomal abnormalitiesMetabolism and Genetic Disorders

Cited by 18