K. Gaudenz

发表

Piwi Is Required in Multiple Cell Types to Control Germline Stem Cell Lineage Development in the Drosophila Ovary

J. Haug, A. Perera, T. Xie, 2014, PloS one.

A Complex Oscillating Network of Signaling Genes Underlies the Mouse Segmentation Clock

Jie Chen, Arcady Mushegian, Earl F. Glynn, 2006, Science.

Defective FGF signaling causes coloboma formation and disrupts retinal neurogenesis

T. Xie, C. Seidel, C. Deng, 2012, Cell Research.

Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function

Earl F. Glynn, E. Glynn, M. Dixon, 2008, Nature Medicine.

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.

E. Haan, R. Markowitz, A. Guttmacher, 1997, American journal of human genetics.

Stable transgenesis in Astyanax mexicanus using the Tol2 transposase system

A. Keene, Nicolas Rohner, James B Jaggard, 2019, bioRxiv.

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

S. Scherer, L. Tsui, M. Muenke, 1996, Nature Genetics.

Analysis of patients with craniosynostosis syndromes for a pro246Arg mutation of FGFR4.

K. Alitalo, M. Muenke, K. Gaudenz, 1998, Molecular genetics and metabolism.

Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domain.

A. Ballabio, J. Opitz, B. Wittwer, 1998, American journal of human genetics.

Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly

S. Scherer, L. Tsui, M. Muenke, 1997, Human Genetics.

N-cadherin expression level distinguishes reserved versus primed states of hematopoietic stem cells.

Xi C. He, J. Haug, Linheng Li, 2007, Cell stem cell.

Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly.

S. Scherer, L. Tsui, M. Muenke, 1997, Human molecular genetics.

Transcription Alters Chromosomal Locations of Cohesin in Saccharomyces cerevisiae

J. Gerton, C. Seidel, K. Gaudenz, 2007, Molecular and Cellular Biology.

Analysis of dynamic changes in retinoid-induced transcription and epigenetic profiles of murine Hox clusters in ES cells

Brian D. Slaughter, R. Krumlauf, A. Shilatifard, 2015, Genome research.

Delayed Correlation of mRNA and Protein Expression in Rapamycin-treated Cells and a Role for Ggc1 in Cellular Sensitivity to Rapamycin*

Norman Pavelka, Earl F. Glynn, Mihaela E. Sardiu, 2009, Molecular & Cellular Proteomics.

Notch2 regulates BMP signaling and epithelial morphogenesis in the ciliary body of the mouse eye

T. Xie, A. Kiernan, R. Libby, 2013, Proceedings of the National Academy of Sciences.

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

George J. Feldman, Andrea Ballabio, Maximilian Muenke, 1997, Nature Genetics.

Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

E. Zackai, M. Muenke, G. Bellus, 1996, Nature Genetics.

Improved transcription and translation with L-leucine stimulation of mTORC1 in Roberts syndrome

J. Gerton, Baoshan Xu, K. Gaudenz, 2016, BMC Genomics.

Identification of a genetic cause for isolated unilateral coronal synostosis: a unique mutation in the fibroblast growth factor receptor 3.

E. Zackai, S. Bartlett, K. Gripp, 1998, The Journal of pediatrics.

Insulin resistance in cavefish as an adaptation to a nutrient-limited environment

Misty R. Riddle, C. Tabin, Nicolas Rohner, 2017, Nature.

Poised RNA polymerase II changes over developmental time and prepares genes for future expression.

Alexander S. Garruss, J. Zeitlinger, R. Krumlauf, 2012, Cell reports.

Wingless Directly Represses DPP Morphogen Expression via an Armadillo/TCF/Brinker Complex

H. Theisen, J. Purcell, A. Syed, 2007, PloS one.

Twisted gastrulation is a conserved extracellular BMP antagonist

Stephen C. Ekker, Spencer Hermanson, Osamu Shimmi, 2001, Nature.

The Twisted gastrulation family of proteins, together with the IGFBP and CCN families, comprise the TIC superfamily of cysteine rich secreted factors

J. Marsh, K. Gaudenz, Z. Hegedus, 2001, Molecular pathology : MP.

Improved transcription and translation with L-leucine stimulation of mTORC1 in Roberts syndrome

J. Gerton, Baoshan Xu, K. Gaudenz, 2016, BMC Genomics.

Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly

S. Scherer, L. Tsui, S. Antonarakis, 1998, Human Genetics.

N-cadherin expression level distinguishes reserved versus primed states of hematopoietic stem cells.

Xi C. He, J. Haug, Linheng Li, 2007, Cell stem cell.

Erratum: Opiz G/BBB syndrome in Xp22: Mutations in the MID1 gene cluster in the carboxy-terminal domain (American Journal of Human Genetics (September 1998) 63 (703-710))

A. Ballabio, B. Wittwer, M. Muenke, 1998 .