Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Melissa L. Berry"'
Autor:
John P. Sundberg, Dale A. Begley, Melissa L. Berry, Michelle N. Perry, David Shaw, Paul N. Schofield
Publikováno v:
Pathology of Genetically Engineered and Other Mutant Mice. :22-38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ad5dc90c693b9bdd1c692ca3252a290
https://doi.org/10.1002/9781119624608.ch3
https://doi.org/10.1002/9781119624608.ch3
Publikováno v:
Lab animal. 49(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e36c6651afb9963477bcd067d55689d4
https://pubmed.ncbi.nlm.nih.gov/31802010
https://pubmed.ncbi.nlm.nih.gov/31802010
Autor:
Ronald G. Gregg, Gobinda Pangeni, Laura G. Reinholdt, Neal S. Peachey, Samantha Burrill, Son Yong Karst, Bernard FitzMaurice, Maureen A. McCall, Nazarul Hasan, Marge Strobel, Melissa L. Berry, Bo Chang
Publikováno v:
Journal of Neurophysiology. 118:845-854
This article describes a mouse model of the human disease complete congenital stationary night blindness in which the mutation reduces but does not eliminate GRM6 expression and bipolar cell function, a phenotype distinct from that seen in other Grm6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5d4572a8c2231c03ac04eec79477c38
https://doi.org/10.1152/jn.00888.2016
https://doi.org/10.1152/jn.00888.2016
Publikováno v:
Lab Animal. 49:9-10
Many studies have reported on the identification of ‘essential genes’ in mice, but the context of the experimental model, including genetic background and specific molecular details of the allele, may impact the influence of alleles on viability.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8a8b212eb19ec14df103568a039b94c
https://doi.org/10.1038/s41684-019-0444-1
https://doi.org/10.1038/s41684-019-0444-1
Autor:
Neal S, Peachey, Nazarul, Hasan, Bernard, FitzMaurice, Samantha, Burrill, Gobinda, Pangeni, Son Yong, Karst, Laura, Reinholdt, Melissa L, Berry, Marge, Strobel, Ronald G, Gregg, Maureen A, McCall, Bo, Chang
Publikováno v:
Journal of neurophysiology. 118(2)
This article describes a mouse model of the human disease complete congenital stationary night blindness in which the mutation reduces but does not eliminate GRM6 expression and bipolar cell function, a phenotype distinct from that seen in other Grm6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b50d8201d490b0a18ca47a259c862ea8
https://pubmed.ncbi.nlm.nih.gov/28490646
https://pubmed.ncbi.nlm.nih.gov/28490646
Autor:
Laura G. Reinholdt, Amira Masri, Patricia F Ward-Bailey, Abby Tadenev, Jocelyn C. Sharp, Anne Czechanski, Robert W. Burgess, Candice Byers, Anuj Srivastava, Jeffrey Milbrandt, Belinda S. Harris, Hanan Hamamy, Periklis Makrythanasis, Stylianos E. Antonarakis, Gregory A. Cox, Rangjiao Liu, Stephen A. Murray, Coleen Kane, Jay Shendure, Whitney Martin, Polyxeni Gudis, Federico Santoni, Bo Chang, Anuradha Lakshminarayana, Paul F. Cliften, Laurent P. Bogdanik, Ian Greenstein, Kristina Palmer, Louise A Dionne, Heather Fairfield, Martin Kircher, C. Herbert Pratt, Son Yong Karst, Melissa L. Berry, David E. Bergstrom, Michelle Curtain, Leah Rae Donahue, Guruprasad Ananda, David G. Schroeder
Publikováno v:
Genome Research, Vol. 25, No 7 (2015) pp. 948-957
Genome Res, vol. 25, no. 7, pp. 948-57
GENOME RESEARCH
Genome Res, vol. 25, no. 7, pp. 948-57
GENOME RESEARCH
Spontaneously arising mouse mutations have served as the foundation for understanding gene function for more than 100 years. We have used exome sequencing in an effort to identify the causative mutations for 172 distinct, spontaneously arising mouse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7d929619ef8a01cd99b8ef1fb6b5e99
https://europepmc.org/articles/PMC4484392/
https://europepmc.org/articles/PMC4484392/
Autor:
Danielle Milette, Annabelle C.O. Chong, Evica Rajcan-Separovic, Brett S. Abrahams, Maimun Nisha, Farkhad Muratkhodjaev, Elizabeth M. Simpson, Melissa L Berry, David A. Brewster, Sabine Mai
Publikováno v:
genesis. 36:134-141
The evolving trend to use larger transgenes and their associated increased chance of unexpected genetic events mandates more careful characterization of transgenic mice. In characterizing our five new mouse strains transgenic for the BAC, bEMS4, we h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d22ba7768fba83d4663663d901e88f4
https://doi.org/10.1002/gene.10205
https://doi.org/10.1002/gene.10205
Autor:
Diana L. Palmquist, Brett S. Abrahams, Byrappa Venkatesh, Elizabeth M. Simpson, Melissa L Berry, Sydney Brenner, Alice Tay, Y. H. Tan, Grace M Mak, Jennifer R Saionz
Publikováno v:
Genomics. 80:45-53
Fierce (frc) mice are deleted for nuclear receptor 2e1 (Nr2e1), and exhibit cerebral hypoplasia, blindness, and extreme aggression. To characterize the Nr2e1 locus, which may also contain the mouse kidney disease (kd) allele, we compared sequence fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4042649030b4e52e4aa45e37c233a9c
https://doi.org/10.1006/geno.2002.6795
https://doi.org/10.1006/geno.2002.6795
Autor:
Melissa L. Berry, Carol C. Linder
Publisher Summary The use of mice in biomedical research greatly facilitates the understanding of human biology and is critical for the development of treatment for diseases. The phenotypic characteristics and pathophysiology of mice carrying spontan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac55175923b9125756597136d5c727f9
https://doi.org/10.1016/b978-012369454-6/50016-9
https://doi.org/10.1016/b978-012369454-6/50016-9
Autor:
Kelly A. Young, Melissa L Berry, Richard S. Smith, Jennifer R Saionz, Elizabeth M. Simpson, Randy J. Nelson, Roderick T. Bronson, Bo Chang, Connie L Mahaffey, Qing Yin Zheng, Norman L. Hawes
Publikováno v:
Behavioural brain research. 132(2)
A new spontaneous mouse mutation named fierce (frc) is deleted for the nuclear receptor Nr2e1 gene (also known as Tlx, mouse homolog of Drosophila tailless). The fierce mutation is genetically and phenotypically similar to Nr2e1 targeted mutations pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78c5cb903ceb934f8650279aeb4ffd27
https://pubmed.ncbi.nlm.nih.gov/11997145
https://pubmed.ncbi.nlm.nih.gov/11997145