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Items: 1 to 50 of 72

1.

Optical imaging with a novel cathepsin-activatable probe for enhanced detection of colorectal cancer.

Esfahani SA, Heidari P, Kucherlapati MH, Ferrer JM, Kucherlapati RS, Mahmood U.

Am J Nucl Med Mol Imaging. 2019 Oct 15;9(5):230-242. eCollection 2019.

2.

Cardiovascular disease in Noonan syndrome.

Prendiville TW, Gauvreau K, Tworog-Dube E, Patkin L, Kucherlapati RS, Roberts AE, Lacro RV.

Arch Dis Child. 2014 Jul;99(7):629-34. Epub 2014 Feb 17.

PMID:
24534818
3.

Genotype directed therapy in murine mismatch repair deficient tumors.

Kucherlapati MH, Esfahani S, Habibollahi P, Wang J, Still ER, Bronson RT, Mahmood U, Kucherlapati RS.

PLoS One. 2013 Jul 23;8(7):e68817. doi: 10.1371/journal.pone.0068817. Print 2013.

4.

Medical complications, clinical findings, and educational outcomes in adults with Noonan syndrome.

Smpokou P, Tworog-Dube E, Kucherlapati RS, Roberts AE.

Am J Med Genet A. 2012 Dec;158A(12):3106-11. doi: 10.1002/ajmg.a.35639. Epub 2012 Nov 19.

PMID:
23165751
5.

Impaired lymphatic contraction associated with immunosuppression.

Liao S, Cheng G, Conner DA, Huang Y, Kucherlapati RS, Munn LL, Ruddle NH, Jain RK, Fukumura D, Padera TP.

Proc Natl Acad Sci U S A. 2011 Nov 15;108(46):18784-9. doi: 10.1073/pnas.1116152108. Epub 2011 Nov 7. Erratum in: Proc Natl Acad Sci U S A. 2016 Oct 4;113(40):E5992.

6.

A restricted spectrum of NRAS mutations causes Noonan syndrome.

Cirstea IC, Kutsche K, Dvorsky R, Gremer L, Carta C, Horn D, Roberts AE, Lepri F, Merbitz-Zahradnik T, König R, Kratz CP, Pantaleoni F, Dentici ML, Joshi VA, Kucherlapati RS, Mazzanti L, Mundlos S, Patton MA, Silengo MC, Rossi C, Zampino G, Digilio C, Stuppia L, Seemanova E, Pennacchio LA, Gelb BD, Dallapiccola B, Wittinghofer A, Ahmadian MR, Tartaglia M, Zenker M.

Nat Genet. 2010 Jan;42(1):27-9. doi: 10.1038/ng.497. Epub 2009 Dec 6.

7.

Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia.

Kratz CP, Niemeyer CM, Thomas C, Bauhuber S, Matejas V, Bergsträsser E, Flotho C, Flores NJ, Haas O, Hasle H, van den Heuvel-Eibrink MM, Kucherlapati RS, Lang P, Roberts AE, Starý J, Strahm B, Swanson KD, Trebo M, Zecca M, Neel B, Locatelli F, Loh ML, Zenker M.

Leukemia. 2007 May;21(5):1108-9. Epub 2007 Feb 22. No abstract available.

PMID:
17315019
8.

Germline gain-of-function mutations in SOS1 cause Noonan syndrome.

Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, Li L, Yassin Y, Tamburino AM, Neel BG, Kucherlapati RS.

Nat Genet. 2007 Jan;39(1):70-4. Epub 2006 Dec 3.

PMID:
17143285
9.

Inactivation of conditional Rb by Villin-Cre leads to aggressive tumors outside the gastrointestinal tract.

Kucherlapati MH, Nguyen AA, Bronson RT, Kucherlapati RS.

Cancer Res. 2006 Apr 1;66(7):3576-83.

10.

The PTPN11 gene is not implicated in nonsyndromic hypertrophic cardiomyopathy.

Roberts AE, Hult B, Rehm HL, Rehm HL, McDonough B, Barr S, Seidman CE, Seidman JG, Kucherlapati RS.

Am J Med Genet A. 2005 Jan 30;132A(3):333-4. No abstract available.

PMID:
15578621
11.

Initial sequencing and comparative analysis of the mouse genome.

Mouse Genome Sequencing Consortium, Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M, An P, Antonarakis SE, Attwood J, Baertsch R, Bailey J, Barlow K, Beck S, Berry E, Birren B, Bloom T, Bork P, Botcherby M, Bray N, Brent MR, Brown DG, Brown SD, Bult C, Burton J, Butler J, Campbell RD, Carninci P, Cawley S, Chiaromonte F, Chinwalla AT, Church DM, Clamp M, Clee C, Collins FS, Cook LL, Copley RR, Coulson A, Couronne O, Cuff J, Curwen V, Cutts T, Daly M, David R, Davies J, Delehaunty KD, Deri J, Dermitzakis ET, Dewey C, Dickens NJ, Diekhans M, Dodge S, Dubchak I, Dunn DM, Eddy SR, Elnitski L, Emes RD, Eswara P, Eyras E, Felsenfeld A, Fewell GA, Flicek P, Foley K, Frankel WN, Fulton LA, Fulton RS, Furey TS, Gage D, Gibbs RA, Glusman G, Gnerre S, Goldman N, Goodstadt L, Grafham D, Graves TA, Green ED, Gregory S, Guigó R, Guyer M, Hardison RC, Haussler D, Hayashizaki Y, Hillier LW, Hinrichs A, Hlavina W, Holzer T, Hsu F, Hua A, Hubbard T, Hunt A, Jackson I, Jaffe DB, Johnson LS, Jones M, Jones TA, Joy A, Kamal M, Karlsson EK, Karolchik D, Kasprzyk A, Kawai J, Keibler E, Kells C, Kent WJ, Kirby A, Kolbe DL, Korf I, Kucherlapati RS, Kulbokas EJ, Kulp D, Landers T, Leger JP, Leonard S, Letunic I, Levine R, Li J, Li M, Lloyd C, Lucas S, Ma B, Maglott DR, Mardis ER, Matthews L, Mauceli E, Mayer JH, McCarthy M, McCombie WR, McLaren S, McLay K, McPherson JD, Meldrim J, Meredith B, Mesirov JP, Miller W, Miner TL, Mongin E, Montgomery KT, Morgan M, Mott R, Mullikin JC, Muzny DM, Nash WE, Nelson JO, Nhan MN, Nicol R, Ning Z, Nusbaum C, O'Connor MJ, Okazaki Y, Oliver K, Overton-Larty E, Pachter L, Parra G, Pepin KH, Peterson J, Pevzner P, Plumb R, Pohl CS, Poliakov A, Ponce TC, Ponting CP, Potter S, Quail M, Reymond A, Roe BA, Roskin KM, Rubin EM, Rust AG, Santos R, Sapojnikov V, Schultz B, Schultz J, Schwartz MS, Schwartz S, Scott C, Seaman S, Searle S, Sharpe T, Sheridan A, Shownkeen R, Sims S, Singer JB, Slater G, Smit A, Smith DR, Spencer B, Stabenau A, Stange-Thomann N, Sugnet C, Suyama M, Tesler G, Thompson J, Torrents D, Trevaskis E, Tromp J, Ucla C, Ureta-Vidal A, Vinson JP, Von Niederhausern AC, Wade CM, Wall M, Weber RJ, Weiss RB, Wendl MC, West AP, Wetterstrand K, Wheeler R, Whelan S, Wierzbowski J, Willey D, Williams S, Wilson RK, Winter E, Worley KC, Wyman D, Yang S, Yang SP, Zdobnov EM, Zody MC, Lander ES.

Nature. 2002 Dec 5;420(6915):520-62.

PMID:
12466850
12.

Genomic and expression analysis of the 12p11-p12 amplicon using EST arrays identifies two novel amplified and overexpressed genes.

Bourdon V, Naef F, Rao PH, Reuter V, Mok SC, Bosl GJ, Koul S, Murty VV, Kucherlapati RS, Chaganti RS.

Cancer Res. 2002 Nov 1;62(21):6218-23.

13.

PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity.

Tartaglia M, Kalidas K, Shaw A, Song X, Musat DL, van der Burgt I, Brunner HG, Bertola DR, Crosby A, Ion A, Kucherlapati RS, Jeffery S, Patton MA, Gelb BD.

Am J Hum Genet. 2002 Jun;70(6):1555-63. Epub 2002 May 1.

14.

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome.

Tartaglia M, Mehler EL, Goldberg R, Zampino G, Brunner HG, Kremer H, van der Burgt I, Crosby AH, Ion A, Jeffery S, Kalidas K, Patton MA, Kucherlapati RS, Gelb BD.

Nat Genet. 2001 Dec;29(4):465-8. Erratum in: Nat Genet 2001 Dec;29(4):491. Nat Genet 2002 Jan;30(1):123.

PMID:
11704759
15.

Initial sequencing and analysis of the human genome.

Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W, Funke R, Gage D, Harris K, Heaford A, Howland J, Kann L, Lehoczky J, LeVine R, McEwan P, McKernan K, Meldrim J, Mesirov JP, Miranda C, Morris W, Naylor J, Raymond C, Rosetti M, Santos R, Sheridan A, Sougnez C, Stange-Thomann Y, Stojanovic N, Subramanian A, Wyman D, Rogers J, Sulston J, Ainscough R, Beck S, Bentley D, Burton J, Clee C, Carter N, Coulson A, Deadman R, Deloukas P, Dunham A, Dunham I, Durbin R, French L, Grafham D, Gregory S, Hubbard T, Humphray S, Hunt A, Jones M, Lloyd C, McMurray A, Matthews L, Mercer S, Milne S, Mullikin JC, Mungall A, Plumb R, Ross M, Shownkeen R, Sims S, Waterston RH, Wilson RK, Hillier LW, McPherson JD, Marra MA, Mardis ER, Fulton LA, Chinwalla AT, Pepin KH, Gish WR, Chissoe SL, Wendl MC, Delehaunty KD, Miner TL, Delehaunty A, Kramer JB, Cook LL, Fulton RS, Johnson DL, Minx PJ, Clifton SW, Hawkins T, Branscomb E, Predki P, Richardson P, Wenning S, Slezak T, Doggett N, Cheng JF, Olsen A, Lucas S, Elkin C, Uberbacher E, Frazier M, Gibbs RA, Muzny DM, Scherer SE, Bouck JB, Sodergren EJ, Worley KC, Rives CM, Gorrell JH, Metzker ML, Naylor SL, Kucherlapati RS, Nelson DL, Weinstock GM, Sakaki Y, Fujiyama A, Hattori M, Yada T, Toyoda A, Itoh T, Kawagoe C, Watanabe H, Totoki Y, Taylor T, Weissenbach J, Heilig R, Saurin W, Artiguenave F, Brottier P, Bruls T, Pelletier E, Robert C, Wincker P, Smith DR, Doucette-Stamm L, Rubenfield M, Weinstock K, Lee HM, Dubois J, Rosenthal A, Platzer M, Nyakatura G, Taudien S, Rump A, Yang H, Yu J, Wang J, Huang G, Gu J, Hood L, Rowen L, Madan A, Qin S, Davis RW, Federspiel NA, Abola AP, Proctor MJ, Myers RM, Schmutz J, Dickson M, Grimwood J, Cox DR, Olson MV, Kaul R, Raymond C, Shimizu N, Kawasaki K, Minoshima S, Evans GA, Athanasiou M, Schultz R, Roe BA, Chen F, Pan H, Ramser J, Lehrach H, Reinhardt R, McCombie WR, de la Bastide M, Dedhia N, Blöcker H, Hornischer K, Nordsiek G, Agarwala R, Aravind L, Bailey JA, Bateman A, Batzoglou S, Birney E, Bork P, Brown DG, Burge CB, Cerutti L, Chen HC, Church D, Clamp M, Copley RR, Doerks T, Eddy SR, Eichler EE, Furey TS, Galagan J, Gilbert JG, Harmon C, Hayashizaki Y, Haussler D, Hermjakob H, Hokamp K, Jang W, Johnson LS, Jones TA, Kasif S, Kaspryzk A, Kennedy S, Kent WJ, Kitts P, Koonin EV, Korf I, Kulp D, Lancet D, Lowe TM, McLysaght A, Mikkelsen T, Moran JV, Mulder N, Pollara VJ, Ponting CP, Schuler G, Schultz J, Slater G, Smit AF, Stupka E, Szustakowki J, Thierry-Mieg D, Thierry-Mieg J, Wagner L, Wallis J, Wheeler R, Williams A, Wolf YI, Wolfe KH, Yang SP, Yeh RF, Collins F, Guyer MS, Peterson J, Felsenfeld A, Wetterstrand KA, Patrinos A, Morgan MJ, de Jong P, Catanese JJ, Osoegawa K, Shizuya H, Choi S, Chen YJ, Szustakowki J; International Human Genome Sequencing Consortium.

Nature. 2001 Feb 15;409(6822):860-921. Erratum in: Nature 2001 Aug 2;412(6846):565. Nature 2001 Jun 7;411(6838):720. Szustakowki, J [corrected to Szustakowski, J].

16.

Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6.

Ion A, Crosby AH, Kremer H, Kenmochi N, Van Reen M, Fenske C, Van Der Burgt I, Brunner HG, Montgomery K, Kucherlapati RS, Patton MA, Page C, Mariman E, Jeffery S.

J Med Genet. 2000 Nov;37(11):884-6. No abstract available.

17.

Heterogeneity in the breakpoints in balanced rearrangements involving band 12p13 in hematologic malignancies identified by fluorescence in situ hybridization: TEL (ETV6 ) is involved in only one half.

Sato Y, Bohlander SK, Kobayashi H, Reshmi S, Suto Y, Davis EM, Espinosa R, Hoopes R, Montgomery KT, Kucherlapati RS, Le Beau MM, Rowley JD.

Blood. 1997 Dec 15;90(12):4886-93.

PMID:
9389705
18.

Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomas.

Schoenberg Fejzo M, Ashar HR, Krauter KS, Powell WL, Rein MS, Weremowicz S, Yoon SJ, Kucherlapati RS, Chada K, Morton CC.

Genes Chromosomes Cancer. 1996 Sep;17(1):1-6.

PMID:
8889500
19.

Assignment of the human myogenic factors 5 and 6 (MYF5, MYF6) gene cluster to 12q21 by in situ hybridization and physical mapping of the locus between D12S350 and D12S106.

Cupelli L, Renault B, Leblanc-Straceski J, Banks A, Ward D, Kucherlapati RS, Krauter K.

Cytogenet Cell Genet. 1996;72(2-3):250-1. No abstract available.

PMID:
8978788
20.

Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.

Lindsay EA, Goldberg R, Jurecic V, Morrow B, Carlson C, Kucherlapati RS, Shprintzen RJ, Baldini A.

Am J Med Genet. 1995 Jul 3;57(3):514-22.

PMID:
7677167
21.

Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases.

Kobayashi H, Montgomery KT, Bohlander SK, Adra CN, Lim BL, Kucherlapati RS, Donis-Keller H, Holt MS, Le Beau MM, Rowley JD.

Blood. 1994 Nov 15;84(10):3473-82.

PMID:
7949101
22.

Mutations in the non-helical linker segment L1-2 of keratin 5 in patients with Weber-Cockayne epidermolysis bullosa simplex.

Chan YM, Yu QC, LeBlanc-Straceski J, Christiano A, Pulkkinen L, Kucherlapati RS, Uitto J, Fuchs E.

J Cell Sci. 1994 Apr;107 ( Pt 4):765-74.

23.

Genomics: stock-taking after 5 years.

McKusik VA, Kucherlapati RS, Ruddle FH.

Genomics. 1993 Jan;15(1):1-2. No abstract available.

PMID:
8432520
24.

Generation of a nested series of interstitial deletions in yeast artificial chromosomes carrying human DNA.

Campbell C, Gulati R, Nandi AK, Floy K, Hieter P, Kucherlapati RS.

Proc Natl Acad Sci U S A. 1991 Jul 1;88(13):5744-8.

25.

Methods for introducing DNA into mammalian cells.

Keown WA, Campbell CR, Kucherlapati RS.

Methods Enzymol. 1990;185:527-37. No abstract available.

PMID:
2381329
26.

Homologous recombination in mammalian somatic cells.

Kucherlapati RS.

Prog Nucleic Acid Res Mol Biol. 1989;36:301-10. Review. No abstract available.

PMID:
2660192
27.

Homologous recombination in a Chinese hamster X-ray-sensitive mutant.

Moore PD, Song KY, Chekuri L, Wallace L, Kucherlapati RS.

Mutat Res. 1986 Apr;160(2):149-55.

PMID:
3951458
28.

Insertion of DNA sequences into the human chromosomal beta-globin locus by homologous recombination.

Smithies O, Gregg RG, Boggs SS, Koralewski MA, Kucherlapati RS.

Nature. 1985 Sep 19-25;317(6034):230-4.

PMID:
2995814
29.

Homologous recombination catalyzed by human cell extracts.

Kucherlapati RS, Spencer J, Moore PD.

Mol Cell Biol. 1985 Apr;5(4):714-20.

30.

Homologous recombination between plasmids in mammalian cells can be enhanced by treatment of input DNA.

Kucherlapati RS, Eves EM, Song KY, Morse BS, Smithies O.

Proc Natl Acad Sci U S A. 1984 May;81(10):3153-7.

31.

Insulin-induced reactivation of an inactive herpes simplex thymidine kinase gene.

Clough DW, Morse BS, Kucherlapati RS, Davidson RL.

Proc Natl Acad Sci U S A. 1984 Feb;81(3):838-42.

32.

Homologous recombination with DNA introduced into mammalian cells.

Smithies O, Koralewski MA, Song KY, Kucherlapati RS.

Cold Spring Harb Symp Quant Biol. 1984;49:161-70. No abstract available.

PMID:
6597754
33.

Homologous recombination in monkey cells and human cell-free extracts.

Kucherlapati RS, Ayares D, Hanneken A, Noonan K, Rauth S, Spencer JM, Wallace L, Moore PD.

Cold Spring Harb Symp Quant Biol. 1984;49:191-7. No abstract available.

PMID:
6099233
34.

Events preceding stable integration of SV40 genomes in a human cell line.

Hwang SP, Kucherlapati RS.

Somatic Cell Genet. 1983 Jul;9(4):457-68.

PMID:
6312621
35.

Modulation of transfected gene expression mediated by changes in chromatin structure.

Davies RL, Fuhrer-Krusi S, Kucherlapati RS.

Cell. 1982 Dec;31(3 Pt 2):521-9.

PMID:
6186385
36.

Activation of human beta-globin genes from nonerythroid cells by fusion with murine erythroleukemia cells.

Pyati J, Kucherlapati RS, Skoultchi AI.

Proc Natl Acad Sci U S A. 1980 Jun;77(6):3435-9.

37.
38.

Assignment of the gene locus for human alpha-L-fucosidase to chromosome 1 by analysis of somatic cell hybrids.

Turner BM, Smith M, Turner VS, Kucherlapati RS, Ruddle FH, Hirschhorn K.

Somatic Cell Genet. 1978 Jan;4(1):45-54.

39.

Human mitochondrial thymidine kinase is coded for by a gene on chromosome 16 of the nucleus.

Willecke K, Teber T, Kucherlapati RS, Ruddle FH.

Somatic Cell Genet. 1977 May;3(3):237-45.

PMID:
605384
40.

Somatic cell genetic assignment of the human gene for mitochondrial NADP-linked isocitrate dehydrogenase to the long arm of chromosome 15.

Shimizu N, Giles RE, Kucherlapati RS, Shimizu Y, Ruddle FH.

Somatic Cell Genet. 1977 Jan;3(1):47-60.

PMID:
564083
41.

Assignment of a human gene for tryptophanyl-tRNA synthetase to chromosome 14 using human-mouse somatic cell hybrids.

Shimizu N, Kucherlapati RS, Ruddle FH.

Somatic Cell Genet. 1976 Jul;2(4):345-57.

PMID:
829178
42.

Detection of interspecific translocations in mouse-human hybrids by alkaline Giemsa staining.

Friend KK, Dorman BP, Kucherlapati RS, Ruddle FH.

Exp Cell Res. 1976 Apr;99(1):31-6. No abstract available.

PMID:
57063
43.

beta2-microglobulin locus on human chromosome 15.

Faber HE, Kucherlapati RS, Poulik MD, Ruddle FH, Smithies O.

Somatic Cell Genet. 1976 Mar;2(2):141-53.

PMID:
69326
44.

Assignment of the human gene for tryptophanyl-tRNA synthetase using human-mouse somatic cell hybrids.

Shimizu N, Kucherlapati RS, Ruddle FH.

Cytogenet Cell Genet. 1976;16(1-5):223-6. No abstract available.

PMID:
1088821
45.

Segregation of human mitochondrial thymidine thymidine kinase activity in human-mouse somatic cell hybrids.

Willecke K, Reber T, Kucherlapati RS, Ruddle FH.

Birth Defects Orig Artic Ser. 1976;12(7):252-5. No abstract available.

PMID:
1024620
46.

Immunochemical detection of human enzymes in hybrid cells.

Shimizu N, Shimizu Y, Kucherlapati RS, Ruddle FH.

Cell. 1976 Jan;7(1):123-30.

PMID:
985736
47.

A new technique for mapping the human hemoglobin genes.

Anderson WF, Deisseroth AB, Velez R, Nienhuis AW, Ruddle FH, Kucherlapati RS.

Cytogenet Cell Genet. 1976;16(1-5):367-71. No abstract available.

PMID:
975910
48.

Segregation of human mitochondrial thymidine kinase activity in human-mouse somatic cell hybrids.

Willecke K, Reber T, Kucherlapati RS, Ruddle FH.

Cytogenet Cell Genet. 1976;16(1-5):252-5. No abstract available.

PMID:
975885
49.

Assignment of the human genes for mannose phosphate isomerase, pyruvate kinase (M2), and hexosaminidase-A to chromosome 15.

Kucherlapati RS, Ruddle FH.

Cytogenet Cell Genet. 1976;16(1-5):181-3. No abstract available.

PMID:
975875
50.

A new technique for mapping the human hemoglobin genes.

Anderson WF, Deisseroth AB, Velez R, Nienhuis AW, Ruddle FH, Kucherlapati RS.

Birth Defects Orig Artic Ser. 1976;12(7):367-71. No abstract available.

PMID:
799520

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