S. Pierce

发表

Genomic binding by the Drosophila Myc, Max, Mad/Mnt transcription factor network.

B. Edgar, H. Bussemaker, J. Delrow, 2003, Genes & development.

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

A. Singleton, C. Baker, E. Eichler, 2008, Science.

Drosophila growth and development in the absence of dMyc and dMnt.

J. Delrow, R. Eisenman, C. Yost, 2008, Developmental biology.

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy

R. Pfundt, Adam Claridge‐Chang, B. Venkatesh, 2020, Nature Communications.

Overexpression of Xgsk-3 disrupts anterior ectodermal patterning in Xenopus.

S. Pierce, D. Kimelman, 1996, Developmental biology.

Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families

T. Walsh, M. King, Ming K. Lee, 2016, European Journal of Human Genetics.

Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy.

T. Walsh, M. King, M. Tekin, 2014, The New England journal of medicine.

Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria

Michael S. Bereman, M. King, M. MacCoss, 2011, Proceedings of the National Academy of Sciences.

Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome.

T. Walsh, M. King, Ming K. Lee, 2013, American journal of human genetics.

Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophrenia.

Bradley P. Coe, B. Coe, Niklas Krumm, 2013, American journal of human genetics.

Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism.

T. Walsh, M. King, J. Lupski, 2015, The Journal of clinical endocrinology and metabolism.

Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities

M. King, S. Pierce, B. Norquist, 2020, Cold Spring Harbor molecular case studies.

dMyc is required for larval growth and endoreplication in Drosophila

J. S. Britton, B. Edgar, R. Eisenman, 2004, Development.

Myc A Weapon of Mass Destruction

R. Eisenman, S. Pierce, J. Secombe, 2004, Cell.

Interaction among Gsk-3, Gbp, Axin, and APC in Xenopus Axis Specification

D. M. Ferkey, C. Yost, S. Pierce, 2000, The Journal of cell biology.

GBP, an Inhibitor of GSK-3, Is Implicated in Xenopus Development and Oncogenesis

D. M. Ferkey, C. Yost, S. Pierce, 1998, Cell.

Histone Acetyltransferase Activity of p300 Is Required for Transcriptional Repression by the Promyelocytic Leukemia Zinc Finger Protein

J. Licht, M. Isalan, S. Pierce, 2004, Molecular and Cellular Biology.

Inherited thrombocytopenia associated with mutation of UDP‐galactose‐4‐epimerase (GALE)

T. Walsh, M. King, S. Pierce, 2018, Human molecular genetics.

Regulation of Spemann organizer formation by the intracellular kinase Xgsk-3.

S. Pierce, D. Kimelman, S B Pierce, 1995, Development.

Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome

T. Walsh, M. King, J. Opitz, 2011, Proceedings of the National Academy of Sciences.

Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome.

T. Walsh, M. King, J. Opitz, 2010, American journal of human genetics.

De novo mutation in RING1 with epigenetic effects on neurodevelopment

T. Walsh, M. King, J. McClellan, 2018, Proceedings of the National Academy of Sciences.

Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.

J. Sebat, T. Walsh, M. King, 2010, American journal of human genetics.

Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease

Tom Walsh, Augusto Morales, T. Walsh, 2016, Cold Spring Harbor molecular case studies.

Mutations in Twinkle primase-helicase cause Perrault syndrome with neurologic features

T. Walsh, M. King, Ming K. Lee, 2014, Neurology.

Regulation of DAF-2 receptor signaling by human insulin and ins-1, a member of the unusually large and diverse C. elegans insulin gene family.

Michael A. Costa, Leo X. Liu, G. Ruvkun, 2001, Genes & development.

The receptor for insulin‐like growth factor II mediates an insulin‐like response.

S. Pierce, D. Morgan, R. Roth, 1987, The EMBO journal.