Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Thomas H. Roderick"'
Autor:
Raquel Pittiglio, Beth A. Marosy, Ethylin Wang Jabs, P Calvas, Nicolas Chassaing, Roxann G. Ingersoll, Jill A. Barton, Alan F. Scott, David W. Mohr, Shreya S. Prabhu, Thomas H. Roderick, William C. Bromley, Brian Craig, Laura Kasch, Kimberly F. Doheny
Publikováno v:
JAMA Ophthalmology
JAMA Ophthalmology, American Medical Association 2014, 132 (10), pp.1215. ⟨10.1001/jamaophthalmol.2014.1731⟩
JAMA Ophthalmology, American Medical Association 2014, 132 (10), pp.1215. ⟨10.1001/jamaophthalmol.2014.1731⟩
International audience; Importance: Microphthalmias are rare disorders whose genetic bases are not fully understood. HMGB3 is a new candidate gene for X-linked forms of this disease.Objective: To identify the causative gene in a pedigree with an X-li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::485582e5d8fe88c73552beb129ca692f
https://hal-univ-tlse3.archives-ouvertes.fr/hal-03240874
https://hal-univ-tlse3.archives-ouvertes.fr/hal-03240874
Autor:
Christopher J. Calvano, James Mandell, Susan A. Cook, Norman L. Hawes, Kenneth R. Johnson, Thomas H. Roderick, Muriel T. Davisson, Roderick T. Bronson, Ellen C. Akeson
Publikováno v:
Cytogenetic and Genome Research. 93:77-82
The paracentric inversion In(3)55Rk on mouse Chromosome 3 (Chr 3) was induced by cesium irradiation. Genetic crosses indicate the proximal breakpoint cosegregates with D3Mit324 and D3Mit92; the distal breakpoint cosegregates with D3Mit127, D3Mit160,
Autor:
A. Rapoport, Steven Nusinowitz, Natik I. Piriev, Muriel T. Davisson, John R. Heckenlively, Christine A. Kozak, Patsy M. Nishina, Norman L. Hawes, Debora B. Farber, Bo Chang, Michael Danciger, Thomas H. Roderick, N. B. Akhmedov
Publikováno v:
Proceedings of the National Academy of Sciences. 97:5551-5556
The rd7 mouse, an animal model for hereditary retinal degeneration, has some characteristics similar to human flecked retinal disorders. Here we report the identification of a deletion in a photoreceptor-specific nuclear receptor (mPNR) mRNA that is
Autor:
Xin Wang, John R. Heckenlively, Richard S. Smith, Norman L. Hawes, Muriel T. Davisson, Bo Chang, Ellen C. Akeson, Xiaohua Gong, Thomas H. Roderick
Publikováno v:
Genomics. 63:314-320
A new cataract mutation was discovered in an ongoing program to identify new mouse models of hereditary eye disease. Lens opacity 12 (Lop12) is a semidominant mutation that results in an irregular nuclear lens opacity similar to the human Coppock cat
Autor:
Kevin Flurkey, Thomas H. Roderick, J. Chen, M.C. Astle, Jonathan R. Archer, David E. Harrison, Simon Klebanov
Publikováno v:
Genetica. 110:209-218
We found high narrow-sense heritability of life span based on the regression of offspring on average parental (midparent) life spans. In two mouse populations prepared using the 4-way-cross design, mean ± SE heritabilities were 62 ± 11% (P ≤ 0.00
Publikováno v:
Genomics. 42:393-396
An autosomal dominant retinal degeneration, called Rd4, was found in a stock carrying the inversion In(4)56Rk, which was induced in a DBA/2J male. The inversion encompasses nearly all of Chromosome 4. It is homozygous lethal and in heterozygotes is a
Autor:
Gregory S. Hageman, Norman L. Hawes, Thomas H. Roderick, Lawrence C. Erway, Chen Peng, Bo Chang, John R. Heckenlively
Publikováno v:
Proceedings of the National Academy of Sciences. 92:11100-11104
Usher syndrome is a group of diseases with autosomal recessive inheritance, congenital hearing loss, and the development of retinitis pigmentosa, a progressive retinal degeneration characterized by night blindness and visual field loss over several d
Autor:
Kenneth P. LeClair, Charles P. Hart, Frank H. Ruddle, Thomas H. Roderick, A. Zelent, Lisa Hunihan, John G. Compton, Stephen H. Langley
Publikováno v:
Journal of Experimental Zoology. 263:83-95
We have identified restriction fragment length polymorphisms between Mus musculus and Mus spretus for the Chromosome 15 loci Hox-3, Wnt-1, Krt-2, Rar-g, and Ly-6. We followed the inheritance of these alleles in interspecific genetic test crosses betw
Publikováno v:
Mammalian Genome. 1:S1-S17
Autor:
Norman L. Hawes, John Taylor, M. Anne Gemmell, Sandra L. Tollaksen, Carol S. Giometti, Thomas H. Roderick
Publikováno v:
Mutation Research/Genetic Toxicology. 242:47-55
We have used two-dimensional gel electrophoresis (2DE) coupled with computer-assisted data analysis to analyze liver-protein expression in mice known to be heterozygous carriers of recessive lethal mutations induced in In(1)1Rk or In(7)13Rk inversion