Zobrazeno 1 - 10
of 28
pro vyhledávání: '"L R, Donahue"'
Autor:
L. R. Donahue, Wesley G. Beamer, Mary L. Bouxsein, N. Pitner, Charles H. Turner, R. Price, J. Schriefer, Qiwei Sun, Clifford J. Rosen, K. L. Shultz
Publikováno v:
Calcified Tissue International. 73:297-303
Genetic linkage studies in C3H/HeJ (C3H) and C57BL/6J (B6) mice identified several chromosomal locations or quantitative trait loci (QTL) linked to femoral volumetric bone mineral density (vBMD). From QTL identified on chromosomes (chr) 1, 4, 6, 13,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab00f9436556f279de72f2ade0123a04
https://doi.org/10.1007/s00223-002-1062-1
https://doi.org/10.1007/s00223-002-1062-1
Autor:
Kin-Hing William Lau, L. R. Donahue, Donna D. Strong, Weikuan Gu, Xin-Min Li, Wesley G. Beamer, Subburaman Mohan, Bouchra Edderkaoui, David J. Baylink
Publikováno v:
Genetica. 114:1-9
One QTL and genes and phenotypes have been localized in the region between 92 cM and 95 cM of mouse chromosome 1. The QTL locus contributes to approximately 40% of the variation of the peak bone density between C57BL/6J (B6) and CAST/EiJ (CAST) strai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e81ddc44798cf745fd8773ee3bebf696
https://doi.org/10.1023/a:1014609809681
https://doi.org/10.1023/a:1014609809681
Autor:
C J, Rosen, G A, Churchill, L R, Donahue, K L, Shultz, J K, Burgess, D R, Powell, C, Ackert, W G, Beamer
Publikováno v:
Bone. 27:521-528
Serum insulin-like growth factor-1 (IGF-1) and femoral bone mineral density (BMD) differ between two inbred strains of mice, C3H/HeJ (C3H) and C57BL/6J (B6), by approximately 30% and 50%, respectively. Similarly, skeletal IGF-1 content, bone formatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e51db92f8b2c0ea42f71302fe10bd032
https://doi.org/10.1016/s8756-3282(00)00354-9
https://doi.org/10.1016/s8756-3282(00)00354-9
Autor:
Kenneth R. Johnson, L. R. Donahue, Roderick T. Bronson, Jerry R. Faust, Priscilla W. Lane, Allison Tanner
Publikováno v:
American Journal of Medical Genetics. 77:289-297
The neuronal ceroid lipofuscinoses (NCLs) comprise a set of at least 6 distinct human and an unknown number of animal diseases characterized by storage of proteolipids in lysosomes of many cell types. By unknown mechanisms, this accumulation leads to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b572a8bba5c7692aba281f77d9d61cb4
https://doi.org/10.1002/(sici)1096-8628(19980526)77:4<289::aid-ajmg8>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19980526)77:4<289::aid-ajmg8>3.0.co
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
Publikováno v:
Mammalian Genome. 8:108-112
Cerebellar deficient folia, cdf, is a spontaneous autosomal recessive mutation in the mouse with unique pathology; the cerebellar cortex of the cdf/cdf mouse has only 7 folia instead of 10, which is the normal count for the C3H/HeJ strain in which th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ceeb66dbf93f5f8650f8d44a74b95132
https://doi.org/10.1007/s003359900368
https://doi.org/10.1007/s003359900368
Publikováno v:
Mammalian Genome. 7:871-876
Megencephaly, enlarged brain, occurs in several acquired and inherited human diseases including Sotos syndrome, Robinow syndrome, Canavan's disease, and Alexander disease. This defect can be distinguished from macrocephaly, an enlarged head, which us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d491adb274e9f8965716be8665c2fb7c
https://doi.org/10.1007/s003359900259
https://doi.org/10.1007/s003359900259
Publikováno v:
Journal of Heredity. 87:87-95
Mesenchymal dysplasia (mes) is a new autosomal recessive mouse mutation that alters normal growth of mesenchyme-derived tissues and provides a new mouse model for studying connective tissue development and defects. Mutants are characterized by preaxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a964732e8894f4fa1a8b35a3c1b39a24
https://doi.org/10.1093/oxfordjournals.jhered.a022981
https://doi.org/10.1093/oxfordjournals.jhered.a022981
Publikováno v:
Journal of Endocrinology. 139:431-439
Insulin-like growth factor-I (IGF-I) and testosterone are major hormonal regulators of protein metabolism. We chose genetically GH-deficient little (lit/lit) mice to test whether these anabolic hormones act independently or in concert with each other
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b7d38eb34e0ff5f0f0c0fa25396cb27
https://doi.org/10.1677/joe.0.1390431
https://doi.org/10.1677/joe.0.1390431
Autor:
Lindsay G. Horton, Boguslawa Koczon-Jaremko, Krista M. Delahunty, Joseph A. Lorenzo, L. R. Donahue, K. L. Shultz, Cheryl L. Ackert-Bicknell, Clifford J. Rosen, Martin L. Adamo, Wesley G. Beamer, Gloria Gronowicz, Barbara E. Kream
Publikováno v:
Endocrinology. 147(8)
We identified quantitative trait loci (QTL) that determined the genetic variance in serum IGF-I through genome-wide scanning of mice derived from C57BL/6J(B6) × C3H/HeJ(C3H) intercrosses. One QTL (Igf1s2), on mouse chromosome 10 (Chr10), produces a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cf0451492668fd273fcf75b7c5b72ee
https://pubmed.ncbi.nlm.nih.gov/16675518
https://pubmed.ncbi.nlm.nih.gov/16675518