K R Thomas
Overview
Explore the profile of K R Thomas including associated specialties, affiliations and a list of published articles.
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40
Citations
2465
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Recent Articles
11.
Thomas K
Psychoanal Rev
. 1995 Dec;
82(6):859-901.
PMID: 8657823
The purpose of this paper was to demonstrate how Freudian concepts such as the Oedipus complex, castration anxiety, fear of loss of love, the psychosexual stages of development, and the...
12.
Zeiher B, Eichwald E, Zabner J, Smith J, Puga A, McCray Jr P, et al.
J Clin Invest
. 1995 Oct;
96(4):2051-64.
PMID: 7560099
The most common cause of cystic fibrosis is a mutation that deletes phenylalanine 508 in cystic fibrosis transmembrane conductance regulator (CFTR). The delta F508 protein is misprocessed and degraded rather...
13.
14.
Knapp J, Thomas K, Mathews R, Wasserman G
Pediatr Emerg Care
. 1994 Dec;
10(6):364-8.
PMID: 7899126
No abstract available.
15.
Thompson D, Thomas K, S Fernandez M
Int J Rehabil Res
. 1994 Jun;
17(2):109-21.
PMID: 7960334
The primary purpose of this article is to inform an international audience about the Americans with Disabilities Act, which is considered by some American humanists to be the most significant...
16.
17.
Deng C, Thomas K, Capecchi M
Mol Cell Biol
. 1993 Apr;
13(4):2134-40.
PMID: 8455602
Gene targeting was used to introduce nonselectable genetic changes into chromosomal loci in mouse embryo-derived stem cells. The nonselectable markers were linked to a selectable marker in both insertion- and...
18.
Thomas K
Am J Psychoanal
. 1992 Sep;
52(3):213-25.
PMID: 1443274
Freud's description of his analysis and treatment of the Wolf-Man will be forever regarded as an extraordinary clinical and theoretical achievement. What has been attempted in this paper is to...
19.
Thomas K, Deng C, Capecchi M
Mol Cell Biol
. 1992 Jul;
12(7):2919-23.
PMID: 1620105
Mutations were targeted to the Hprt locus in murine embryonic stem cells by using sequence replacement vectors. When the vector was designed such that the mutated sequences were flanked on...
20.
Thomas K, Musci T, Neumann P, Capecchi M
Cell
. 1991 Nov;
67(5):969-76.
PMID: 1835670
Mice homozygous for the recessive mutation swaying (sw) are characterized by ataxia and hypertonia, attributed to the malformation of anterior regions of the cerebellum. We show that sw is a...