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Showing 1–50 of 67 results

Advanced filters: Author: Neal Copeland Clear advanced filters

Cooperative activation of Hoxa and Pbx1-related genes in murine myeloid leukaemias

Takuro Nakamura
David A. Largaespada
Neal G. Copeland
Research01 Feb 1996
Nature Genetics

Volume: 12, P: 149-153
Evolution of the mammalian G protein α subunit multigene family

Thomas M. Wilkie
Debra J. Gilbert
Neal G. Copeland
Research01 May 1992
Nature Genetics

Volume: 1, P: 85-91
Nf1 deficiency causes Ras-Dediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia

David A. Largaespada
Camilynn I. Brannan
Neal G. Copeland
Research01 Feb 1996
Nature Genetics

Volume: 12, P: 137-143
Dilute (d) coat colour mutation of DBA/2J mice is associated with the site of integration of an ecotropic MuLV genome

Nancy A. Jenkins
Neal G. Copeland
Barbara K. Lee
Research01 Oct 1981
Nature

Volume: 293, P: 370-374
The human pseudoautosomal GM–CSF receptor α subunit gene is autosomal in mouse

Christine M. Disteche
Camilynn I. Brannan
Linda S. Park
Research01 Aug 1992
Nature Genetics

Volume: 1, P: 333-336
Anchored reference loci for comparative genome mapping in mammals

Stephen J. O'Brien
James E. Womack
Neal G. Copeland
Reviews01 Feb 1993
Nature Genetics

Volume: 3, P: 103-112
Sequence homology shared by neurofibromatosis type-1 gene and IRA-1 and IRA-2 negative regulators of the RAS cyclic AMP pathway

Arthur M. Buchberg
Linda S. Cleveland
Neal G. Copeland
Research20 Sept 1990
Nature

Volume: 347, P: 291-294
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

Karen B. Avraham
Tama Hasson
Nancy A. Jenkins
Research01 Dec 1995
Nature Genetics

Volume: 11, P: 369-375
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region

Stuart E. Leff
Camilynn I. Brannan
Nancy A. Jenkins
Research01 Dec 1992
Nature Genetics

Volume: 2, P: 259-264
Proviral integrations at the Evi5 locus disrupt a novel 90 kDa protein with homology to the Tre2 oncogene and cell-cycle regulatory proteins

Xiaobei Liao
Yubin Du
Neal G Copeland
Research06 Mar 1997
Oncogene

Volume: 14, P: 1023-1029
Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia

Takuro Nakamura
David A. Largaespada
John D. Shaughnessy Jr.
Research01 Feb 1996
Nature Genetics

Volume: 12, P: 154-158
Genomic imprinting of Mash2, a mouse gene required for trophoblast development

François Guillemot
Tamara Caspary
András Nagy
Research01 Mar 1995
Nature Genetics

Volume: 9, P: 235-242
A comprehensive genetic map of the mouse genome

William F. Dietrich
Joyce Miller
Eric S. Lander
Research14 Mar 1996
Nature

Volume: 380, P: 149-152
Hyperaccumulation of FAD-linked presenilin 1 variants in vivo

Michael K. Lee
David R. Borchelt
Sangram S. Sisodia
Research01 Jul 1997
Nature Medicine

Volume: 3, P: 756-760
Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

Alex Koufos
Marc F. Hansen
Webster K. Cavenee
Research25 Jul 1985
Nature

Volume: 316, P: 330-334
Project reading

Neal G. Copeland
Comments & Opinion01 Oct 1992
Nature

Volume: 359, P: 440
GHRH receptor of little mice contains a missense mutation in the extracellular domain that disrupts receptor function

Paul Godfrey
Jason O. Rahal
Kelly E. Mayo
Research01 Jul 1993
Nature Genetics

Volume: 4, P: 227-232
Novel myosin heavy chain encoded by murine dilute coat colour locus

John A. Mercer
Peter K. Seperack
Nancy A. Jenkins
Research21 Feb 1991
Nature

Volume: 349, P: 709-713
The itchy locus encodes a novel ubiquitin protein ligase that is disrupted in a^18H mice

William L. Perry
Carolyn M. Hustad
Neal G. Copeland
Research01 Feb 1998
Nature Genetics

Volume: 18, P: 143-146
Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis

Rie Watanabe-Fukunaga
Camilynn I. Brannan
Shigekazu Nagata
Research26 Mar 1992
Nature

Volume: 356, P: 314-317
A candidate mouse model for Prader–Willi syndrome which shows an absence of Snrpn expression

Bruce M. Cattanach
Jacqueline A. Barr
Janet Jones
Research01 Dec 1992
Nature Genetics

Volume: 2, P: 270-274
Transposon mutagenesis identifies genetic drivers of Braf^V600E melanoma

Nancy Jenkins, Neal Copeland and colleagues report the results of a Sleeping Beauty transposon mutagenesis screen in mice carrying a melanocyte-specific inducible Braf^V600E allele. Analysis of transposon insertion sites identified candidate genetic drivers of melanoma.

Michael B Mann
Michael A Black
Nancy A Jenkins
Research13 Apr 2015
Nature Genetics

Volume: 47, P: 486-495
Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences

Eiríkur Steingrímsson
Karen J. Moore
Nancy A. Jenkins
Research01 Nov 1994
Nature Genetics

Volume: 8, P: 256-263
Limb alterations in brachypodism mice due to mutations in a new member of the TGFβ-superfamily

Elaine E. Storm
Thanh V. Huynh
Se-Jin Lee
Research14 Apr 1994
Nature

Volume: 368, P: 639-643
Comparative anchor tagged sequences (CATS) for integrative mapping of mammalian genomes

Leslie A. Lyons
Thomas F. Laughlin
Stephen J. O'Brien
Research01 Jan 1997
Nature Genetics

Volume: 15, P: 47-56
Transposon mutagenesis identifies genes driving hepatocellular carcinoma in a chronic hepatitis B mouse model

Neal Copeland and colleagues use a transposon mutagenesis screen to identify drivers of hepatocellular carcinoma in a mouse model of chronic hepatitis B infection. They find a very large number of candidate driver genes, many of which are implicated in cellular metabolism.

Emilie A Bard-Chapeau
Anh-Tuan Nguyen
Neal G Copeland
Research08 Dec 2013
Nature Genetics

Volume: 46, P: 24-32
Correction: A comprehensive genetic map of the mouse genome

William F. Dietrich
Joyce Miller
Eric S. Lander
Amendments and Corrections09 May 1996
Nature

Volume: 381, P: 172
Correction: Novel myosin heavy chain encoded by murine dilute coat colour locus

John A. Mercer
Peter K. Seperack
Nancy A. Jenkins
Amendments and Corrections08 Aug 1991
Nature

Volume: 352, P: 547
Mammalian mutagenesis using a highly mobile somatic Sleeping Beauty transposon system

Adam J. Dupuy
Keiko Akagi
Nancy A. Jenkins
Research14 Jul 2005
Nature

Volume: 436, P: 221-226
Structure and promoter analysis of murine CAD and ICAD genes

Kohki Kawane
Hidehiro Fukuyama
Shigekazu Nagata
Research27 Aug 1999
Cell Death & Differentiation

Volume: 6, P: 745-752
Recombineering: a powerful new tool for mouse functional genomics

Neal G. Copeland
Nancy A. Jenkins
Donald L. Court
Reviews01 Oct 2001
Nature Reviews Genetics

Volume: 2, P: 769-779
A mouse model for Prader-Willi syndrome imprinting-centre mutations

Tao Yang
Todd E. Adamson
Camilynn I. Brannan
Research01 May 1998
Nature Genetics

Volume: 19, P: 25-31
Leukaemia disease genes: large-scale cloning and pathway predictions

Jiayin Li
Haifa Shen
Neal G. Copeland
Research01 Nov 1999
Nature Genetics

Volume: 23, P: 348-353
Keratinocyte growth factor expression in hormone insensitive prostate cancer

Hing Y Leung
Pyush Mehta
David E Neal
Research28 Aug 1997
Oncogene

Volume: 15, P: 1115-1120
Good genes in bad neighbourhoods

Mary A. Bedell
Nancy A. Jenkins
Neal G. Copeland
News & Views01 Mar 1996
Nature Genetics

Volume: 12, P: 229-232
Author Correction: A recellularized human colon model identifies cancer driver genes

Huanhuan Joyce Chen
Zhubo Wei
Michael L Shuler
Amendments and Corrections03 Jun 2019
Nature Biotechnology

Volume: 37, P: 820
Identification of Vangl2 and Scrb1 as planar polarity genes in mammals

Mireille Montcouquiol
Rivka A. Rachel
Matthew W. Kelley
Research30 Apr 2003
Nature

Volume: 423, P: 173-177
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)

Wei Li
Qing Zhang
Richard T Swank
Research17 Aug 2003
Nature Genetics

Volume: 35, P: 84-89
Direct interaction of microtubule- and actin-based transport motors

Jian-Dong Huang
Scott T. Brady
Nancy A. Jenkins
Research21 Jan 1999
Nature

Volume: 397, P: 267-270
Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease

Scott M. Wilson
Bula Bhattacharyya
Nancy A. Jenkins
Research07 Oct 2002
Nature Genetics

Volume: 32, P: 420-425
New genes involved in cancer identified by retroviral tagging

Takeshi Suzuki
Haifa Shen
Neal G Copeland
Research19 Aug 2002
Nature Genetics

Volume: 32, P: 166-174
Bcl11a is essential for normal lymphoid development

Pentao Liu
Jonathan R Keller
Neal G Copeland
Research28 Apr 2003
Nature Immunology

Volume: 4, P: 525-532
Efficient Cre-loxP–induced mitotic recombination in mouse embryonic stem cells

Pentao Liu
Nancy A. Jenkins
Neal G. Copeland
Research10 Dec 2001
Nature Genetics

Volume: 30, P: 66-72
BCL11A is a triple-negative breast cancer gene with critical functions in stem and progenitor cells

Triple-negative breast cancers (TNBCs) tend to have poor prognosis; however, the mechanisms underlying TNBC pathology are not well understood. Here the authors utilize epidemiologic data and animal models to demonstrate an important role for BCL11A in the genesis and propagation of TNBCs.

Walid T. Khaled
Song Choon Lee
Pentao Liu
ResearchOpen Access09 Jan 2015
Nature Communications

Volume: 6, P: 1-10
Dysregulation of T lymphocyte function in itchy mice: a role for Itch in T_H2 differentiation

Deyu Fang
Chris Elly
Yun-Cai Liu
Research04 Feb 2002
Nature Immunology

Volume: 3, P: 281-287
Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6

Qing Zhang
Baohui Zhao
Richard T. Swank
Research27 Jan 2003
Nature Genetics

Volume: 33, P: 145-153
The E3 ligase Itch negatively regulates inflammatory signaling pathways by controlling the function of the ubiquitin-editing enzyme A20

Noula Shembade
Nicole S Harhaj
Edward W Harhaj
Research03 Feb 2008
Nature Immunology

Volume: 9, P: 254-262
Identification of an organelle receptor for myosin-Va

Xufeng S. Wu
Kang Rao
John A. Hammer III
Research04 Mar 2002
Nature Cell Biology

Volume: 4, P: 271-278
Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1

Marion G Ott
Manfred Schmidt
Manuel Grez
Research02 Apr 2006
Nature Medicine

Volume: 12, P: 401-409
A conditional transposon-based insertional mutagenesis screen for genes associated with mouse hepatocellular carcinoma

Keng et al. characterize the mouse hepatocellular carcinoma genome by using tissue-specific recombinase expression to restrict mobilization of the Sleeping Beauty transposon to the liver. High throughput sequencing of >100,000 insertions sites in mouse tumor nodules identifies potential therapeutic targets.

Vincent W Keng
Augusto Villanueva
David A Largaespada
Research22 Feb 2009
Nature Biotechnology

Volume: 27, P: 264-274

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