Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Patricia F Ward-Bailey"'
Autor:
John P Sundberg, Hannah Galantino-Homer, Heather Fairfield, Patricia F Ward-Bailey, Belinda S Harris, Melissa Berry, C Herbert Pratt, Nicholas E Gott, Lesley S Bechtold, Pauline R Kaplan, Blythe P Durbin-Johnson, David M Rocke, Robert H Rice
Publikováno v:
PLoS ONE, Vol 17, Iss 11, p e0277284 (2022)
Numerous single gene mutations identified in humans and mice result in nail deformities with many similarities between the species. A spontaneous, autosomal, recessive mutation called witch nails (whnl) is described here where the distal nail matrix
Externí odkaz:
https://doaj.org/article/111ba92ac4f542d2b3f9392424ccbb91
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:
Priscilla W. Lane, Muriel T. Davisson, Susan A. Cook, Patricia F Ward-Bailey, L. R. Donahue, Roderick T. Bronson
Publikováno v:
Journal of Heredity. 89:254-257
We describe a new juvenile hair loss mutant in the mouse in which the hair follicle follows irregular pathways to the surface and generally becomes dystrophic when the mouse is about 23 days of age. Skin from mutant mice older than 1 month of age is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::973657cafa8de14854260a401d3408b4
https://doi.org/10.1093/jhered/89.3.254
https://doi.org/10.1093/jhered/89.3.254
Autor:
Leonard D. Shultz, Howard C. Passmore, V. Patel, Muriel T. Davisson, Damian Heine, Patricia F Ward-Bailey, Susan A. Cook
Publikováno v:
Mammalian Genome. 7:497-500
The goal of this study was to determine the effect of the mouse severe combined immunodeficiency (scid) mutation on the rate of meiotic recombination, by standard backcross linkage analysis. For this purpose, we examined four crosses that involved F1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5c3b4709afef8735857fa2d9a52a9e5
https://doi.org/10.1007/s003359900150
https://doi.org/10.1007/s003359900150
Publikováno v:
Genomics. 29:457-464
Dactylaplasia is an inherited mouse limb malformation whose manifestation is clearly dependent on the interaction of two genes and thus represents an excellent model system for studying such gene interactions in vivo. The Dac mutation is inherited as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aa8b282348a6c5c3f0cdd5fe4b73b23
https://doi.org/10.1006/geno.1995.9981
https://doi.org/10.1006/geno.1995.9981
Publikováno v:
Mammalian Genome. 4:49-52
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6eca31b4bfae80824fc0eedbeba1feb6
https://doi.org/10.1007/bf00364664
https://doi.org/10.1007/bf00364664
Autor:
Patricia F Ward-Bailey, Muriel T. Davisson, Michael Bustin, Susan A. Cook, Kenneth R. Johnson
Publikováno v:
Mammalian Genome. 4:83-89
HMG-17 is an abundant, nonhistone chromosomal protein that binds preferentially to nucleosomal core particles of mammalian chromatin. The human gene for HMG-17 has been localized to Chromosome (Chr) 1p, but the murine gene has not been previously map
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6058229682e03b442f9f54df021597a6
https://doi.org/10.1007/bf00290431
https://doi.org/10.1007/bf00290431
Autor:
Muriel T. Davisson, Leah Rae Donahue, Susan A. Cook, Kenneth R. Johnson, Belinda S. Harris, Patricia F Ward-Bailey, Roderick T. Bronson
Publikováno v:
Mammalian Genome. 11:1139-1141
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc17aa022687234f0943d1d8e72bf0c7
https://doi.org/10.1007/s003350010165
https://doi.org/10.1007/s003350010165
Autor:
Leona H. Gagnon, Leah Rae Donahue, Coleen C. Marden, Patricia F Ward-Bailey, Kenneth R. Johnson, Roderick T. Bronson
Publikováno v:
Molecular endocrinology (Baltimore, Md.). 21(7)
Dual oxidases generate the hydrogen peroxide needed by thyroid peroxidase for the incorporation of iodine into thyroglobulin, an essential step in thyroid hormone synthesis. Mutations in the human dual oxidase 2 gene, DUOX2, have been shown to underl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b68e46c3ceb30af221bef979c6e66cab
https://pubmed.ncbi.nlm.nih.gov/17440044
https://pubmed.ncbi.nlm.nih.gov/17440044
Autor:
Bonnie Wood, Kenneth R. Johnson, Rod Bronson, Patricia F Ward-Bailey, Leah Rae Donahue, Muriel T. Davisson
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 11(10)
Neuromuscular ataxia, nma, is a new autosomal recessive mutation that arose spontaneously in CBA/J inbred mice at The Jackson Laboratory. The mutation, now maintained on the B6C3FeF(1) hybrid background, when homozygous, causes small size, uncoordina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0693cb0a154dfb9165d2ebe4ceaa9d1b
https://pubmed.ncbi.nlm.nih.gov/11003693
https://pubmed.ncbi.nlm.nih.gov/11003693