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Items: 1 to 50 of 57

1.

Feasibility of spatial frequency-domain imaging for monitoring palpable breast lesions.

Robbins CM, Raghavan G, Antaki JF, Kainerstorfer JM.

J Biomed Opt. 2017 Aug;22(12):1-9. doi: 10.1117/1.JBO.22.12.121605.

PMID:
28831792
2.

8q24 risk alleles and prostate cancer in African-Barbadian men.

Cropp CD, Robbins CM, Sheng X, Hennis AJ, Carpten JD, Waterman L, Worrell R, Schwantes-An TH, Trent JM, Haiman CA, Leske MC, Wu SY, Bailey-Wilson JE, Nemesure B.

Prostate. 2014 Dec;74(16):1579-88. doi: 10.1002/pros.22871. Epub 2014 Sep 22.

3.

Integrating patient safety and clinical pharmacy services into the care of a high-risk, ambulatory population: a collaborative approach.

Robbins CM, Stillwell T, Johnson D, Wilson S, Fitzgerald L.

J Patient Saf. 2013 Jun;9(2):110-7. doi: 10.1097/PTS.0b013e318281b879.

PMID:
23697983
4.

LuxS influences Escherichia coli biofilm formation through autoinducer-2-dependent and autoinducer-2-independent modalities.

Niu C, Robbins CM, Pittman KJ, Osborn jL, Stubblefield BA, Simmons RB, Gilbert ES.

FEMS Microbiol Ecol. 2013 Mar;83(3):778-91. doi: 10.1111/1574-6941.12034. Epub 2012 Nov 26.

5.

Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer.

Zuhlke KA, Johnson AM, Okoth LA, Stoffel EM, Robbins CM, Tembe WA, Salinas CA, Zheng SL, Xu J, Carpten JD, Lange EM, Isaacs WB, Cooney KA.

Fam Cancer. 2012 Dec;11(4):595-600. doi: 10.1007/s10689-012-9555-1.

6.

Germline mutations in HOXB13 and prostate-cancer risk.

Ewing CM, Ray AM, Lange EM, Zuhlke KA, Robbins CM, Tembe WD, Wiley KE, Isaacs SD, Johng D, Wang Y, Bizon C, Yan G, Gielzak M, Partin AW, Shanmugam V, Izatt T, Sinari S, Craig DW, Zheng SL, Walsh PC, Montie JE, Xu J, Carpten JD, Isaacs WB, Cooney KA.

N Engl J Med. 2012 Jan 12;366(2):141-9. doi: 10.1056/NEJMoa1110000.

7.

EphB2 SNPs and sporadic prostate cancer risk in African American men.

Robbins CM, Hooker S, Kittles RA, Carpten JD.

PLoS One. 2011;6(5):e19494. doi: 10.1371/journal.pone.0019494. Epub 2011 May 16.

8.

Copy number and targeted mutational analysis reveals novel somatic events in metastatic prostate tumors.

Robbins CM, Tembe WA, Baker A, Sinari S, Moses TY, Beckstrom-Sternberg S, Beckstrom-Sternberg J, Barrett M, Long J, Chinnaiyan A, Lowey J, Suh E, Pearson JV, Craig DW, Agus DB, Pienta KJ, Carpten JD.

Genome Res. 2011 Jan;21(1):47-55. doi: 10.1101/gr.107961.110. Epub 2010 Dec 8.

9.

Agarose stabilization of fragile biofilms for quantitative structure analysis.

Pittman KJ, Robbins CM, Osborn JL, Stubblefield BA, Gilbert ES.

J Microbiol Methods. 2010 May;81(2):101-7. doi: 10.1016/j.mimet.2010.02.001. Epub 2010 Feb 10.

PMID:
20152866
10.

Sweet syndrome with pulmonary involvement in a healthy young woman.

Robbins CM, Mason SE, Hughey LC.

Arch Dermatol. 2009 Mar;145(3):344-6. doi: 10.1001/archdermatol.2008.610. No abstract available.

PMID:
19289785
11.

Mastectomy with breast reconstruction in previously augmented patients: indications for implant removal.

Robbins CM, Long JN, Fix RJ, de la Torre JI, Vasconez LO.

Ann Plast Surg. 2008 Nov;61(5):500-5. doi: 10.1097/SAP.0b013e31817e9cef.

PMID:
18948775
12.

Association of HPC2/ELAC2 and RNASEL non-synonymous variants with prostate cancer risk in African American familial and sporadic cases.

Robbins CM, Hernandez W, Ahaghotu C, Bennett J, Hoke G, Mason T, Pettaway CA, Vijayakumar S, Weinrich S, Furbert-Harris P, Dunston G, Powell IJ, Carpten JD, Kittles RA.

Prostate. 2008 Dec 1;68(16):1790-7. doi: 10.1002/pros.20841.

13.

Admixture and population stratification in African Caribbean populations.

Benn-Torres J, Bonilla C, Robbins CM, Waterman L, Moses TY, Hernandez W, Santos ER, Bennett F, Aiken W, Tullock T, Coard K, Hennis A, Wu S, Nemesure B, Leske MC, Freeman V, Carpten J, Kittles RA.

Ann Hum Genet. 2008 Jan;72(Pt 1):90-8. Epub 2006 Oct 1.

14.

A transforming mutation in the pleckstrin homology domain of AKT1 in cancer.

Carpten JD, Faber AL, Horn C, Donoho GP, Briggs SL, Robbins CM, Hostetter G, Boguslawski S, Moses TY, Savage S, Uhlik M, Lin A, Du J, Qian YW, Zeckner DJ, Tucker-Kellogg G, Touchman J, Patel K, Mousses S, Bittner M, Schevitz R, Lai MH, Blanchard KL, Thomas JE.

Nature. 2007 Jul 26;448(7152):439-44. Epub 2007 Jul 4.

PMID:
17611497
15.

Fine-mapping the putative chromosome 17q21-22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysis.

Lange EM, Robbins CM, Gillanders EM, Zheng SL, Xu J, Wang Y, White KA, Chang BL, Ho LA, Trent JM, Carpten JD, Isaacs WB, Cooney KA.

Hum Genet. 2007 Mar;121(1):49-55. Epub 2006 Nov 21.

PMID:
17120048
16.

Alefacept in the treatment of psoriatic nail disease: a proof of concept study.

Parrish CA, Sobera JO, Robbins CM, Cantrell WC, Desmond RA, Elewski BE.

J Drugs Dermatol. 2006 Apr;5(4):339-40.

PMID:
16673801
17.

A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.

Kittles RA, Baffoe-Bonnie AB, Moses TY, Robbins CM, Ahaghotu C, Huusko P, Pettaway C, Vijayakumar S, Bennett J, Hoke G, Mason T, Weinrich S, Trent JM, Collins FS, Mousses S, Bailey-Wilson J, Furbert-Harris P, Dunston G, Powell IJ, Carpten JD.

J Med Genet. 2006 Jun;43(6):507-11. Epub 2005 Sep 9.

18.

Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome.

Bradley KJ, Hobbs MR, Buley ID, Carpten JD, Cavaco BM, Fares JE, Laidler P, Manek S, Robbins CM, Salti IS, Thompson NW, Jackson CE, Thakker RV.

J Intern Med. 2005 Jan;257(1):18-26.

19.

Cloning and characterization of an inversion breakpoint at 6q23.3 suggests a role for Map7 in sacral dysgenesis.

Sood R, Bader PI, Speer MC, Edwards YH, Eddings EM, Blair RT, Hu P, Faruque MU, Robbins CM, Zhang H, Leuders J, Morrison K, Thompson D, Schwartzberg PL, Meltzer PS, Trent JM.

Cytogenet Genome Res. 2004;106(1):61-7.

PMID:
15218243
20.

The use of 40% urea cream in the treatment of moccasin tinea pedis.

Elewski BE, Haley HR, Robbins CM.

Cutis. 2004 May;73(5):355-7.

PMID:
15186053
21.

Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.

Simonds WF, Robbins CM, Agarwal SK, Hendy GN, Carpten JD, Marx SJ.

J Clin Endocrinol Metab. 2004 Jan;89(1):96-102.

PMID:
14715834
22.

Mutational analysis of susceptibility genes RNASEL/HPC1, ELAC2/HPC2, and MSR1 in sporadic prostate cancer.

Nupponen NN, Wallén MJ, Ponciano D, Robbins CM, Tammela TL, Vessella RL, Carpten JD, Visakorpi T.

Genes Chromosomes Cancer. 2004 Feb;39(2):119-25.

PMID:
14695991
23.

Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma.

Shattuck TM, Välimäki S, Obara T, Gaz RD, Clark OH, Shoback D, Wierman ME, Tojo K, Robbins CM, Carpten JD, Farnebo LO, Larsson C, Arnold A.

N Engl J Med. 2003 Oct 30;349(18):1722-9.

24.

Cloning and characterization of a novel gene, SHPRH, encoding a conserved putative protein with SNF2/helicase and PHD-finger domains from the 6q24 region.

Sood R, Makalowska I, Galdzicki M, Hu P, Eddings E, Robbins CM, Moses T, Namkoong J, Chen S, Trent JM.

Genomics. 2003 Aug;82(2):153-61.

PMID:
12837266
25.

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.

Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS.

Nature. 2003 May 15;423(6937):293-8. Epub 2003 Apr 25.

26.

High frequency of BRAF mutations in nevi.

Pollock PM, Harper UL, Hansen KS, Yudt LM, Stark M, Robbins CM, Moses TY, Hostetter G, Wagner U, Kakareka J, Salem G, Pohida T, Heenan P, Duray P, Kallioniemi O, Hayward NK, Trent JM, Meltzer PS.

Nat Genet. 2003 Jan;33(1):19-20. Epub 2002 Nov 25.

PMID:
12447372
27.

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome.

Carpten JD, Robbins CM, Villablanca A, Forsberg L, Presciuttini S, Bailey-Wilson J, Simonds WF, Gillanders EM, Kennedy AM, Chen JD, Agarwal SK, Sood R, Jones MP, Moses TY, Haven C, Petillo D, Leotlela PD, Harding B, Cameron D, Pannett AA, Höög A, Heath H 3rd, James-Newton LA, Robinson B, Zarbo RJ, Cavaco BM, Wassif W, Perrier ND, Rosen IB, Kristoffersson U, Turnpenny PD, Farnebo LO, Besser GM, Jackson CE, Morreau H, Trent JM, Thakker RV, Marx SJ, Teh BT, Larsson C, Hobbs MR.

Nat Genet. 2002 Dec;32(4):676-80. Epub 2002 Nov 18.

PMID:
12434154
28.

Identification of six novel genes by experimental validation of GeneMachine predicted genes.

Makalowska I, Sood R, Faruque MU, Hu P, Robbins CM, Eddings EM, Mestre JD, Baxevanis AD, Carpten JD.

Gene. 2002 Feb 6;284(1-2):203-13.

PMID:
11891061
29.

Physical and transcript map of the hereditary prostate cancer region at xq27.

Stephan DA, Howell GR, Teslovich TM, Coffey AJ, Smith L, Bailey-Wilson JE, Malechek L, Gildea D, Smith JR, Gillanders EM, Schleutker J, Hu P, Steingruber HE, Dhami P, Robbins CM, Makalowska I, Carpten JD, Sood R, Mumm S, Reinbold R, Bonner TI, Baffoe-Bonnie A, Bubendorf L, Heiskanen M, Kallioneimi OP, Baxevanis AD, Joseph SS, Zucchi I, Burk RD, Isaacs W, Ross MT, Trent JM.

Genomics. 2002 Jan;79(1):41-50.

PMID:
11827456
30.

Isolation and characterization of the human homeobox gene HOX D1.

Appukuttan B, Sood R, Ott S, Makalowska I, Patel RJ, Wang X, Robbins CM, Brownstein MJ, Stout JT.

Mol Biol Rep. 2000;27(4):195-201.

PMID:
11455954
31.

The community's voice in research.

Macaulay AC, Gibson N, Freeman WL, Commanda LE, McCabe ML, Robbins CM, Twohig PL.

CMAJ. 2001 Jun 12;164(12):1661-3. No abstract available.

32.

Cloning and characterization of 13 novel transcripts and the human RGS8 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus.

Sood R, Bonner TI, Makalowska I, Stephan DA, Robbins CM, Connors TD, Morgenbesser SD, Su K, Faruque MU, Pinkett H, Graham C, Baxevanis AD, Klinger KW, Landes GM, Trent JM, Carpten JD.

Genomics. 2001 Apr 15;73(2):211-22.

PMID:
11318611
33.

Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer.

Xu J, Zheng SL, Carpten JD, Nupponen NN, Robbins CM, Mestre J, Moses TY, Faith DA, Kelly BD, Isaacs SD, Wiley KE, Ewing CM, Bujnovszky P, Chang B, Bailey-Wilson J, Bleecker ER, Walsh PC, Trent JM, Meyers DA, Isaacs WB.

Am J Hum Genet. 2001 Apr;68(4):901-11. Epub 2001 Mar 14.

34.

Positional cloning utilizing genomic DNA microarrays: the Niemann-Pick type C gene as a model system.

Stephan DA, Chen Y, Jiang Y, Malechek L, Gu JZ, Robbins CM, Bittner ML, Morris JA, Carstea E, Meltzer PS, Adler K, Garlick R, Trent JM, Ashlock MA.

Mol Genet Metab. 2000 May;70(1):10-8.

PMID:
10833327
35.

The human RGL (RalGDS-like) gene: cloning, expression analysis and genomic organization.

Sood R, Makalowska I, Carpten JD, Robbins CM, Stephan DA, Connors TD, Morgenbesser SD, Su K, Pinkett HW, Graham CL, Quesenberry MI, Baxevanis AD, Klinger KW, Trent JM, Bonner TI.

Biochim Biophys Acta. 2000 Apr 25;1491(1-3):285-8.

PMID:
10760592
36.

A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region.

Carpten JD, Makalowska I, Robbins CM, Scott N, Sood R, Connors TD, Bonner TI, Smith JR, Faruque MU, Stephan DA, Pinkett H, Morgenbesser SD, Su K, Graham C, Gregory SG, Williams H, McDonald L, Baxevanis AD, Klingler KW, Landes GM, Trent JM.

Genomics. 2000 Feb 15;64(1):1-14.

PMID:
10708513
37.

Cloning, mapping, and expression of a novel brain-specific transcript in the familial dysautonomia candidate region on chromosome 9q31.

Chadwick BP, Leyne M, Gill S, Liebert CB, Mull J, Mezey E, Robbins CM, Pinkett HW, Makalowska I, Maayan C, Blumenfeld A, Axelrod FB, Brownstein M, Gusella JF, Slaugenhaupt SA.

Mamm Genome. 2000 Jan;11(1):81-3. No abstract available.

PMID:
10603000
38.

Localization of a gene for Duane retraction syndrome to chromosome 2q31.

Appukuttan B, Gillanders E, Juo SH, Freas-Lutz D, Ott S, Sood R, Van Auken A, Bailey-Wilson J, Wang X, Patel RJ, Robbins CM, Chung M, Annett G, Weinberg K, Borchert MS, Trent JM, Brownstein MJ, Stout JT.

Am J Hum Genet. 1999 Dec;65(6):1639-46.

39.

Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene.

Chadwick BP, Gill S, Leyne M, Mull J, Liebert CB, Robbins CM, Pinkett HW, Makalowska I, Maayan C, Blumenfeld A, Axelrod FB, Brownstein M, Slaugenhaupt SA.

Gene. 1999 Nov 15;240(1):67-73.

PMID:
10564813
40.

Participatory research maximises community and lay involvement. North American Primary Care Research Group.

Macaulay AC, Commanda LE, Freeman WL, Gibson N, McCabe ML, Robbins CM, Twohig PL.

BMJ. 1999 Sep 18;319(7212):774-8. Review. No abstract available.

41.

Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familial dysautonomia candidate region on 9q31.

Chadwick BP, Mull J, Helbling LA, Gill S, Leyne M, Robbins CM, Pinkett HW, Makalowska I, Maayan C, Blumenfeld A, Axelrod FB, Brownstein M, Gusella JF, Slaugenhaupt SA.

Genomics. 1999 Jun 15;58(3):302-9.

PMID:
10373328
42.

Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays.

Hacia JG, Fan JB, Ryder O, Jin L, Edgemon K, Ghandour G, Mayer RA, Sun B, Hsie L, Robbins CM, Brody LC, Wang D, Lander ES, Lipshutz R, Fodor SP, Collins FS.

Nat Genet. 1999 Jun;22(2):164-7.

PMID:
10369258
43.

Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene.

Stephan DA, Gillanders E, Vanderveen D, Freas-Lutz D, Wistow G, Baxevanis AD, Robbins CM, VanAuken A, Quesenberry MI, Bailey-Wilson J, Juo SH, Trent JM, Smith L, Brownstein MJ.

Proc Natl Acad Sci U S A. 1999 Feb 2;96(3):1008-12.

44.

Effects of a direct-fed yeast culture on enteric microbial populations, fermentation acids, and performance of weanling pigs.

Mathew AG, Chattin SE, Robbins CM, Golden DA.

J Anim Sci. 1998 Aug;76(8):2138-45.

PMID:
9734864
45.

Evolutionary sequence comparisons using high-density oligonucleotide arrays.

Hacia JG, Makalowski W, Edgemon K, Erdos MR, Robbins CM, Fodor SP, Brody LC, Collins FS.

Nat Genet. 1998 Feb;18(2):155-8.

PMID:
9462745
46.

Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human region.

Hirotsune S, Pack SD, Chong SS, Robbins CM, Pavan WJ, Ledbetter DH, Wynshaw-Boris A.

Genome Res. 1997 Jun;7(6):625-34.

47.

Influence of galactosyl lactose on energy and protein digestibility, enteric microflora, and performance of weanling pigs.

Mathew AG, Robbins CM, Chattin SE, Quigley JD 3rd.

J Anim Sci. 1997 Apr;75(4):1009-16.

PMID:
9110214
48.

2006 expressed-sequence tags derived from human chromosome 7-enriched cDNA libraries.

Touchman JW, Bouffard GG, Weintraub LA, Idol JR, Wang L, Robbins CM, Nussbaum JC, Lovett M, Green ED.

Genome Res. 1997 Mar;7(3):281-92.

50.

Developing allantois is a primary site of 2'-deoxycoformycin toxicity.

Airhart MJ, Robbins CM, Knudsen TB, Church JK, Skalko RG.

Teratology. 1996 Jun;53(6):361-73.

PMID:
8910982

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