Niswander, Lee

Hedgehog signalling in the mouse requires intraflagellar transport proteins

Huangfu, D., Liu, A., Rakeman, A. S., Murcia, N. S., Niswander, L., & Anderson, K. V. (2003) · Nature

Hedgehog Signaling Pathway StudiesGenetic and Kidney Cyst Diseases

Cited by 1,425

β-catenin activation is necessary and sufficient to specify the dorsal dermal fate in the mouse

Atit, R., Sgaier, S. K., Mohamed, O. A., Taketo, M. M., Dufort, D., Joyner, A. L., Niswander, L., & Conlon, R. A. (2006) · Developmental Biology

Developmental Biology and Gene RegulationWnt/β-catenin signaling in development and cancer

Cited by 400

LDL-receptor-related protein 4 is crucial for formation of the neuromuscular junction

Weatherbee, S. D., Anderson, K. V., & Niswander, L. A. (2006) · Development

Myasthenia Gravis and ThymomaMuscle Physiology and Disorders

Cited by 351

Coordinate regulation of neural tube patterning and proliferation by TGFβ and WNT activity

Chesnutt, C., Burrus, L. W., Brown, A. M. C., & Niswander, L. (2004) · Developmental Biology

Developmental Biology and Gene RegulationWnt/β-catenin signaling in development and cancer

Cited by 152

Lin28 promotes the proliferative capacity of neural progenitor cells in brain development

Yang, M., Yang, S.-L., Herrlinger, S., Liang, C., Dzieciatkowska, M., Hansen, K. C., Desai, R., Nagy, A., Niswander, L., Moss, E. G., et al. (2015) · Development

Neurogenesis and neuroplasticity mechanismsDevelopmental Biology and Gene Regulation

Cited by 127

The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin disease.

Zohn, I. E., De Domenico, I., Pollock, A., Ward, D. M., Goodman, J. F., Liang, X., Sanchez, A. J., Niswander, L., & Kaplan, J. (2007) · Blood

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 104

Scribble is required for normal epithelial cell–cell contacts and lumen morphogenesis in the mammalian lung

Yates, L. L., Schnatwinkel, C., Hazelwood, L., Chessum, L., Paudyal, A., Hilton, H., Romero, M. R., Wilde, J., Bogani, D., Sanderson, J., et al. (2013) · Developmental Biology

Developmental Biology and Gene RegulationHippo pathway signaling and YAP/TAZ

Cited by 78

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

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

A hypomorphic allele reveals an important role of inturned in mouse skeletal development

Chang, R., Petersen, J. R., Niswander, L. A., & Liu, A. (2015) · Developmental Dynamics

Genetic and Kidney Cyst DiseasesHedgehog Signaling Pathway Studies

Cited by 18