Y. You

发表

Generation of inner ear sensory neurons using blastocyst complementation in a Neurog1+/−−deficient mouse

J. Dutton, W. Low, P. Santi, 2020, Stem cell research & therapy.

Modification of an Existing Chromosomal Inversion to Engineer a Balancer for Mouse Chromosome 15

W. S. Chick, D. Carpenter, E. Rinchik, 2004, Genetics.

Leiomodin-3-deficient mice display nemaline myopathy with fast-myofiber atrophy

Ling V. Sun, Sheng Ding, Xiaohui Wu, 2015, Disease Models & Mechanisms.

Decreasing mutant ATXN1 nuclear localization improves a spectrum of SCA1-like phenotypes and brain region transcriptomic profiles

Jason S. Mitchell, H. Zoghbi, H. Orr, 2022, Neuron.

Liver development is restored by blastocyst complementation of HHEX knockout in mice and pigs

J. Dutton, C. Steer, W. Low, 2021, Stem cell research & therapy.

A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice.

J. Sundberg, A. Christiano, D. Warburton, 2008, Human molecular genetics.

Homozygous carnitine palmitoyltransferase 1b (muscle isoform) deficiency is lethal in the mouse.

P. A. Wood, T. Schoeb, C. Hoppel, 2005, Molecular genetics and metabolism.

Physical mapping of male fertility and meiotic drive quantitative trait loci in the mouse t complex using chromosome deficiencies.

J. Schimenti, A. Planchart, Y. You, 2000, Genetics.

Deletion mapping of the head tilt (het) gene in mice: a vestibular mutation causing specific absence of otoliths.

M. Lyon, J. Schimenti, L. Erway, 1998, Genetics.

Chromosomal deletion complexes in mice by radiation of embryonic stem cells

Rudolf Jaenisch, Heather Nelson, R. Jaenisch, 1997, Nature Genetics.

The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered Hoxc gene expression in the ears.

J. Sundberg, D. Carpenter, E. Rinchik, 2008, Veterinary dermatology.

X-ray-induced deletion complexes in embryonic stem cells on mouse chromosome 15

W. S. Chick, Dabney K. Johnson, D. Carpenter, 2005, Mammalian Genome.

Regional vulnerability in a neurodegenerative disease: Delineating SCA1 CNS and muscle therapeutic targets using a conditional mutant ATXN1 mouse.

Jason S. Mitchell, H. Zoghbi, J. Ervasti, 2023, bioRxiv : the preprint server for biology.

Decreasing mutant ATXN1 nuclear localization improves a spectrum of SCA1-like phenotypes and brain region transcriptomic profiles

Jason S. Mitchell, H. Zoghbi, H. Orr, 2022, Neuron.

Overlapping deletions spanning the proximal two-thirds of the mouse t complex.

D. Bergstrom, J. Schimenti, R. Munroe, 2003, Mammalian genome : official journal of the International Mammalian Genome Society.

Overlapping deletions define novel embryonic lethal loci in the mouse t complex

J. Schimenti, Y. You, Sarah E. Mentzer, 2003, Genesis.

Generation of radiation-induced deletion complexes in the mouse genome using embryonic stem cells.

J. Schimenti, V. Browning, Y. You, 1997, Methods.

A Vector with a Single Promoter for In Vitro Transcription and Mammalian Cell Expression of CRISPR gRNAs

P. Romanienko, Y. You, Willie H. Mark, 2016, PloS one.

Disrupting ATXN1 Nuclear Localization in a Knock-in SCA1 Mouse Model Improves a Spectrum of SCA1-Like Phenotypes and their Brain Region Associated Transcriptomic Profiles

H. Zoghbi, H. Orr, C. Henzler, 2021, bioRxiv.

Utility of C57BL/6J × 129/SvJae embryonic stem cells for generating chromosomal deletions: tolerance to γ radiation and microsatellite polymorphism

R. Jaenisch, J. Schimenti, Y. You, 1998, Mammalian Genome.