Lele KP - Search Results

1

Recent experience in prenatal fra(X) detection.

Jenkins EC, Brown WT, Krawczun MS, Duncan CJ, Lele KP, Cantu ES, Schonberg S, Golbus MS, Sekhon GS, Stark S, et al. Jenkins EC, et al. Among authors: lele kp. Am J Med Genet. 1988 May-Jun;30(1-2):329-36. doi: 10.1002/ajmg.1320300133. Am J Med Genet. 1988. PMID: 2972205

2

Progress toward an internal control system for fragile-X induction by 5-fluorodeoxyuridine in whole-blood cultures.

Jenkins EC, Duncan CJ, Sanz MM, Genovese M, Gu H, Schwartz-Richstein C, Lele KP, Salandi ML, Krawczun MS. Jenkins EC, et al. Among authors: lele kp. Pathobiology. 1990;58(4):236-40. doi: 10.1159/000163591. Pathobiology. 1990. PMID: 2147548

3

Fragile X expression increased by low cell-culture density.

Krawczun MS, Lele KP, Jenkins EC, Brown WT. Krawczun MS, et al. Among authors: lele kp. Am J Med Genet. 1986 Jan-Feb;23(1-2):467-73. doi: 10.1002/ajmg.1320230138. Am J Med Genet. 1986. PMID: 2937301

4

Constitutive fragile sites in fra(X) individuals.

Jenkins EC, Lele KP, Krawczun MS, Gross AC, Duncan CJ, Brown WT. Jenkins EC, et al. Among authors: lele kp. Am J Med Genet. 1988 May-Jun;30(1-2):429-34. doi: 10.1002/ajmg.1320300144. Am J Med Genet. 1988. PMID: 3052066

5

Fragile X chromosome frequency is consistent temporally and within replicate cultures.

Jenkins EC, Kastin BR, Krawczun MS, Lele KP, Silverman WP, Brown WT. Jenkins EC, et al. Among authors: lele kp. Am J Med Genet. 1986 Jan-Feb;23(1-2):475-81. doi: 10.1002/ajmg.1320230139. Am J Med Genet. 1986. PMID: 3953660

6

Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome.

Jenkins EC, Genovese MJ, Duncan CJ, Gu H, Stark-Houck SL, Lele K, Li SY, Krawczun MS. Jenkins EC, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):136-41. doi: 10.1002/ajmg.1320430121. Am J Med Genet. 1992. PMID: 1605182

7

Study of spindle microtubule reassembly in cells from Alzheimer and Down syndrome patients following exposure to colcemid.

Krawczun MS, Jenkins EC, Lele KP, Sersen EA, Wisniewski HM. Krawczun MS, et al. Among authors: lele kp. Alzheimer Dis Assoc Disord. 1990 Winter;4(4):203-16. doi: 10.1097/00002093-199040400-00002. Alzheimer Dis Assoc Disord. 1990. PMID: 2148262

8

Low frequencies of apparently fragile X chromosomes in normal control cultures: a possible explanation.

Jenkins EC, Brown WT, Brooks J, Duncan CJ, Sanz MM, Silverman WP, Lele KP, Masia A, Katz E, Lubin RA, et al. Jenkins EC, et al. Among authors: lele kp. Exp Cell Biol. 1986;54(1):40-8. doi: 10.1159/000163342. Exp Cell Biol. 1986. PMID: 3956839

9

Cytogenetic studies of hairy cell leukemia.

Lele KP, Filippa DA, Chaganti RS. Lele KP, et al. Cancer Genet Cytogenet. 1981 Dec;4(4):325-30. doi: 10.1016/0165-4608(81)90029-7. Cancer Genet Cytogenet. 1981. PMID: 7332900

10

Cytogenetic and molecular analysis of human male germ cell tumors: chromosome 12 abnormalities and gene amplification.

Samaniego F, Rodriguez E, Houldsworth J, Murty VV, Ladanyi M, Lele KP, Chen QG, Dmitrovsky E, Geller NL, Reuter V, et al. Samaniego F, et al. Among authors: lele kp. Genes Chromosomes Cancer. 1990 Mar;1(4):289-300. doi: 10.1002/gcc.2870010406. Genes Chromosomes Cancer. 1990. PMID: 2177638

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