Found: 28
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Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis.
- Published in:
- 2010
- By:
- Publication type:
- journal article
The COP9 signalosome is vital for timely repair of DNA double-strand breaks.
- Published in:
- Nucleic Acids Research, 2015, v. 43, n. 9, p. 4517, doi. 10.1093/nar/gkv270
- By:
- Publication type:
- Article
The fusion gene Cbfb-MYH11 blocks myeloid differentiation and predisposes mice to acute myelomonocytic leukaemia.
- Published in:
- Nature Genetics, 1999, v. 23, n. 2, p. 144, doi. 10.1038/13776
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- Publication type:
- Article
Improved generation of C57BL/6J mouse embryonic stem cells in a defined serum-free media (This article is a US Government work and, as such, is in the public domain in the United States of America.).
- Published in:
- Genesis: The Journal of Genetics & Development, 2004, v. 39, n. 2, p. 100, doi. 10.1002/gene.20031
- By:
- Publication type:
- Article
Direct removal in the mouse of a floxed neo gene from a three-loxp conditional knockout allele by two novel approaches.
- Published in:
- Genesis: The Journal of Genetics & Development, 2001, v. 30, n. 1, p. 1, doi. 10.1002/gene.1025
- By:
- Publication type:
- Article
Meeting the needs of consumers: Lessons from business and industry.
- Published in:
- New Directions for Adult & Continuing Education, 2003, v. 2003, n. 100, p. 89, doi. 10.1002/ace.122
- By:
- Publication type:
- Article
Natural Resource Conservation in a Cultural Park: Evaluating the Importance of Big Hole National Battlefield to the Endemic Lemhi Penstemon (Penstemon lemhiensis).
- Published in:
- Natural Areas Journal, 2013, v. 33, n. 1, p. 50, doi. 10.3375/043.033.0106
- By:
- Publication type:
- Article
Sharing the Patient Experience: A "Talk Story" Intervention for Heart Failure Management in Native Hawaiians.
- Published in:
- Journal of Patient Experience, 2020, v. 7, n. 3, p. 399, doi. 10.1177/2374373519846661
- By:
- Publication type:
- Article
Wnt-5a inhibits the canonical Wnt pathway by promoting GSK-3—independent β-catenin degradation.
- Published in:
- Journal of Cell Biology, 2003, v. 162, n. 5, p. 899, doi. 10.1083/jcb.200303158
- By:
- Publication type:
- Article
Woodland Dynamics at the Northern Range Periphery: A Challenge for Protected Area Management in a Changing World.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0070454
- By:
- Publication type:
- Article
Distribution of American pikas in a low-elevation lava landscape: conservation implications from the range periphery.
- Published in:
- Journal of Mammalogy, 2010, v. 91, n. 5, p. 1287, doi. 10.1644/09-MAMM-A-334.1
- By:
- Publication type:
- Article
An inbred 129SvEv GFPCre transgenic mouse that deletes loxP‐flanked genes in all tissues.
- Published in:
- Nucleic Acids Research, 2003, v. 31, n. 10, p. e57, doi. 10.1093/nar/gng057
- By:
- Publication type:
- Article
Cre-mediated gene deletion in the mammary gland.
- Published in:
- Nucleic Acids Research, 1997, v. 25, n. Supplement, p. 4323, doi. 10.1093/nar/25.21.4323
- By:
- Publication type:
- Article
Highly Efficient Cpf1-Mediated Gene Targeting in Mice Following High Concentration Pronuclear Injection.
- Published in:
- G3: Genes | Genomes | Genetics, 2017, v. 7, n. 2, p. 719, doi. 10.1534/g3.116.038091
- By:
- Publication type:
- Article
addendum: An expressed pseudogene regulates the messenger-RNA stability of its homologous coding gene.
- Published in:
- 2003
- By:
- Publication type:
- Correction Notice
An expressed pseudogene regulates the messenger-RNA stability of its homologous coding gene.
- Published in:
- Nature, 2003, v. 423, n. 6935, p. 91, doi. 10.1038/nature01535
- By:
- Publication type:
- Article
Incidence and Risk Factors for New and Recurrent Infarcts in Adults With Sickle Cell Disease.
- Published in:
- Journal of the American Heart Association, 2024, v. 13, n. 12, p. 1, doi. 10.1161/JAHA.123.033278
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- Publication type:
- Article
A mouse model of Proteus syndrome.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 17, p. 2920, doi. 10.1093/hmg/ddz116
- By:
- Publication type:
- Article
Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral Phenotype.
- Published in:
- Cerebral Cortex, 2015, v. 25, n. 10, p. 3572, doi. 10.1093/cercor/bhu196
- By:
- Publication type:
- Article
CRISPR-Mediated Triple Knockout of SLAMF1, SLAMF5 and SLAMF6 Supports Positive Signaling Roles in NKT Cell Development.
- Published in:
- PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0156072
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- Publication type:
- Article
The ubiquitin ligase SCF<sup>Grr1</sup> is necessary for pheromone sensitivity in Saccharomyces cerevisiae.
- Published in:
- Yeast, 2005, v. 22, n. 7, p. 553, doi. 10.1002/yea.1234
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- Publication type:
- Article
Development and analysis of transgenic mice expressing porcine hematopoietic cytokines: a model for achieving durable porcine hematopoietic chimerism across an extensive xenogeneic barrier.
- Published in:
- Xenotransplantation, 2000, v. 7, n. 1, p. 58, doi. 10.1034/j.1399-3089.2000.00044.x
- By:
- Publication type:
- Article
A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosis.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 17, p. 2501, doi. 10.1093/hmg/ddi254
- By:
- Publication type:
- Article
The MFSD12 p.Tyr182His common variant is sufficient to alter mouse agouti coat color.
- Published in:
- Pigment Cell & Melanoma Research, 2024, v. 37, n. 2, p. 259, doi. 10.1111/pcmr.13144
- By:
- Publication type:
- Article
Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA.
- Published in:
- Nature Genetics, 1998, v. 20, n. 2, p. 198, doi. 10.1038/2510
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- Publication type:
- Article
Ke Ku'una Na'au: A Native Hawaiian Behavioral Health Initiative at The Queen's Medical Center.
- Published in:
- Hawaii Journal of Medicine & Public Health, 2019, v. 78, p. 83
- By:
- Publication type:
- Article
Author Correction: Mutations in COMP cause familial carpal tunnel syndrome.
- Published in:
- 2020
- By:
- Publication type:
- Correction Notice
Mutations in COMP cause familial carpal tunnel syndrome.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-17378-z
- By:
- Publication type:
- Article