Year |
Citation |
Score |
2002 |
Cushman LJ, Showalter AD, Rhodes SJ. Genetic defects in the development and function of the anterior pituitary gland. Annals of Medicine. 34: 179-91. PMID 12173688 DOI: 10.1080/Ann.34.3.179.191 |
0.393 |
|
2001 |
Cushman LJ, Camper SA. Molecular basis of pituitary dysfunction in mouse and human. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 485-94. PMID 11420609 DOI: 10.1007/S003350040002 |
0.594 |
|
2001 |
Zhao L, Bakke M, Krimkevich Y, Cushman LJ, Parlow AF, Camper SA, Parker KL. Hypomorphic phenotype in mice with pituitary-specific knockout of steroidogenic factor 1. Genesis (New York, N.Y. : 2000). 30: 65-9. PMID 11416865 DOI: 10.1002/Gene.1034 |
0.573 |
|
2001 |
Cushman LJ, Watkins-Chow DE, Brinkmeier ML, Raetzman LT, Radak AL, Lloyd RV, Camper SA. Persistent Prop1 expression delays gonadotrope differentiation and enhances pituitary tumor susceptibility. Human Molecular Genetics. 10: 1141-53. PMID 11371507 DOI: 10.1093/Hmg/10.11.1141 |
0.599 |
|
2001 |
Zhao L, Bakke M, Krimkevich Y, Cushman LJ, Parlow AF, Camper SA, Parker KL. Steroidogenic factor 1 (SF1) is essential for pituitary gonadotrope function. Development (Cambridge, England). 128: 147-54. PMID 11124111 |
0.614 |
|
2000 |
Cushman LJ, Burrows HL, Seasholtz AF, Lewandoski M, Muzyczka N, Camper SA. Cre-mediated recombination in the pituitary gland. Genesis (New York, N.Y. : 2000). 28: 167-74. PMID 11105060 DOI: 10.1002/1526-968X(200011/12)28:3/4<167::Aid-Gene120>3.0.Co;2-N |
0.571 |
|
2000 |
Cushman LJ, Burrows HL, Seasholtz AF, Lewandoski M, Muzyczka N, Camper SA. Mouse embryonic stem (ES) cell lines established from neuronal cell-derived cloned blastocysts Genesis. 28: 156-163. PMID 11105058 DOI: 10.1002/1526-968X(200011/12)28:3/4<156::Aid-Gene100>3.0.Co;2-T |
0.536 |
|
Low-probability matches (unlikely to be authored by this person) |
2005 |
Cushman LJ, Torres-Martinez W, Cherry AM, Manning MA, Abdul-Rahman O, Anderson CE, Punnett HH, Thurston VC, Sweeney D, Vance GH. A report of three patients with an interstitial deletion of chromosome 15q24. American Journal of Medical Genetics. Part A. 137: 65-71. PMID 16007617 DOI: 10.1002/ajmg.a.30836 |
0.12 |
|
2005 |
Foroud T, Pankratz N, Batchman AP, Pauciulo MW, Vidal R, Miravalle L, Goebel HH, Cushman LJ, Azzarelli B, Horak H, Farlow M, Nichols WC. A mutation in myotilin causes spheroid body myopathy. Neurology. 65: 1936-40. PMID 16380616 DOI: 10.1212/01.Wnl.0000188872.28149.9A |
0.104 |
|
2005 |
Cushman LJ, Torres-Martinez W, Weaver DD. Johnson-McMillin syndrome: report of a new case with novel features. Birth Defects Research. Part a, Clinical and Molecular Teratology. 73: 638-41. PMID 16116593 DOI: 10.1002/bdra.20178 |
0.079 |
|
2007 |
Cushman L, Warren ML, Livesay S. Bringing research to the bedside: The role of induced hypothermia in cardiac arrest Critical Care Nursing Quarterly. 30: 143-153. PMID 17356355 DOI: 10.1097/01.CNQ.0000264257.75252.41 |
0.074 |
|
2014 |
Quaid KA, Cushman LJ. Genetic counseling Molecular Genetic Pathology: Second Edition. 645-652. DOI: 10.1007/978-1-4614-4800-6-24 |
0.039 |
|
Hide low-probability matches. |