Fremont V - Search Results

1

Regulation of uptake of 18F-FDG by a follicular human thyroid cancer cell line with mutation-activated K-ras.

Prante O, Maschauer S, Fremont V, Reinfelder J, Stoehr R, Szkudlinski M, Weintraub B, Hartmann A, Kuwert T. Prante O, et al. Among authors: fremont v. J Nucl Med. 2009 Aug;50(8):1364-70. doi: 10.2967/jnumed.109.062331. J Nucl Med. 2009. PMID: 19652218 Free article.

2

Effects of recombinant human thyroid-stimulating hormone superagonists on thyroidal uptake of 18F-fluorodeoxyglucose and radioiodide.

Reinfelder J, Maschauer S, Foss CA, Nimmagadda S, Fremont V, Wolf V, Weintraub BD, Pomper MG, Szkudlinski MW, Kuwert T, Prante O. Reinfelder J, et al. Among authors: fremont v. Thyroid. 2011 Jul;21(7):783-92. doi: 10.1089/thy.2010.0394. Epub 2011 May 13. Thyroid. 2011. PMID: 21568725

3

(99m)Tc-labeled-rhTSH analogue (TR1401) for imaging poorly differentiated metastatic thyroid cancer.

Galli F, Manni I, Piaggio G, Balogh L, Weintraub BD, Szkudlinski MW, Fremont V, Dierckx RA, Signore A. Galli F, et al. Among authors: fremont v. Thyroid. 2014 Aug;24(8):1297-308. doi: 10.1089/thy.2013.0429. Epub 2014 Jun 20. Thyroid. 2014. PMID: 24801227 Free PMC article.

4

Thyroid-stimulating hormone and thyroid-stimulating hormone receptor structure-function relationships.

Szkudlinski MW, Fremont V, Ronin C, Weintraub BD. Szkudlinski MW, et al. Among authors: fremont v. Physiol Rev. 2002 Apr;82(2):473-502. doi: 10.1152/physrev.00031.2001. Physiol Rev. 2002. PMID: 11917095 Free article. Review.

5

Human alpha-subunit analogs act as partial agonists to the thyroid-stimulating hormone receptor: differential effects of free and yoked subunits.

Angelova K, Fremont V, Jain R, Zhang M, Puett D, Narayan P, Szkudlinski MW. Angelova K, et al. Among authors: fremont v. Endocrine. 2004 Jun;24(1):25-31. doi: 10.1385/ENDO:24:1:025. Endocrine. 2004. PMID: 15249700

6

The extracellular domain suppresses constitutive activity of the transmembrane domain of the human TSH receptor: implications for hormone-receptor interaction and antagonist design.

Zhang M, Tong KP, Fremont V, Chen J, Narayan P, Puett D, Weintraub BD, Szkudlinski MW. Zhang M, et al. Among authors: fremont v. Endocrinology. 2000 Sep;141(9):3514-7. doi: 10.1210/endo.141.9.7790. Endocrinology. 2000. PMID: 10965926

7

Structure-activity relationship study of a scorpion toxin with high affinity for apamin-sensitive potassium channels by means of the solution structure of analogues.

Inisan AG, Meunier S, Fedelli O, Altbach M, Fremont V, Sabatier JM, Thévan A, Bernassau JM, Cambillau C, Darbon H. Inisan AG, et al. Among authors: fremont v. Int J Pept Protein Res. 1995 May;45(5):441-50. doi: 10.1111/j.1399-3011.1995.tb01059.x. Int J Pept Protein Res. 1995. PMID: 7591483

8

Leiurotoxin I, a scorpion toxin specific for Ca(2+)-activated K+ channels. Structure-activity analysis using synthetic analogs.

Sabatier JM, Fremont V, Mabrouk K, Crest M, Darbon H, Rochat H, Van Rietschoten J, Martin-Eauclaire MF. Sabatier JM, et al. Among authors: fremont v. Int J Pept Protein Res. 1994 May;43(5):486-95. doi: 10.1111/j.1399-3011.1994.tb00548.x. Int J Pept Protein Res. 1994. PMID: 8070973

9

Solution structure of P01, a natural scorpion peptide structurally analogous to scorpion toxins specific for apamin-sensitive potassium channel.

Blanc E, Fremont V, Sizun P, Meunier S, Van Rietschoten J, Thevand A, Bernassau JM, Darbon H. Blanc E, et al. Among authors: fremont v. Proteins. 1996 Mar;24(3):359-69. doi: 10.1002/(SICI)1097-0134(199603)24:3<359::AID-PROT9>3.0.CO;2-B. Proteins. 1996. PMID: 8778783

10

Characterization of PO1, a new peptide ligand of the apamin-sensitive Ca2+ activated K+ channel.

Zerrouk H, Laraba-Djebari F, Fremont V, Meki A, Darbon H, Mansuelle P, Oughideni R, van Rietschoten J, Rochat H, Martin-Eauclaire MF. Zerrouk H, et al. Among authors: fremont v. Int J Pept Protein Res. 1996 Dec;48(6):514-21. doi: 10.1111/j.1399-3011.1996.tb00870.x. Int J Pept Protein Res. 1996. PMID: 8985784

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