Robbins LS - Search Results

1

Isolation of TSH and LH/CG receptor cDNAs from human thyroid: regulation by tissue specific splicing.

Frazier AL, Robbins LS, Stork PJ, Sprengel R, Segaloff DL, Cone RD. Frazier AL, et al. Among authors: robbins ls. Mol Endocrinol. 1990 Aug;4(8):1264-76. doi: 10.1210/mend-4-8-1264. Mol Endocrinol. 1990. PMID: 2293030

2

Thyrotropin receptor messenger ribonucleic acid is expressed in most brown and white adipose tissues in the guinea pig.

Roselli-Rehfuss L, Robbins LS, Cone RD. Roselli-Rehfuss L, et al. Among authors: robbins ls. Endocrinology. 1992 Apr;130(4):1857-61. doi: 10.1210/endo.130.4.1547715. Endocrinology. 1992. PMID: 1547715

3

Cloning and expression of a 5HT7 receptor from Xenopus laevis.

Nelson CS, Cone RD, Robbins LS, Allen CN, Adelman JP. Nelson CS, et al. Among authors: robbins ls. Recept Channels. 1995;3(1):61-70. Recept Channels. 1995. PMID: 8589994

4

The cloning of a family of genes that encode the melanocortin receptors.

Mountjoy KG, Robbins LS, Mortrud MT, Cone RD. Mountjoy KG, et al. Among authors: robbins ls. Science. 1992 Aug 28;257(5074):1248-51. doi: 10.1126/science.1325670. Science. 1992. PMID: 1325670

5

Cloning and functional characterization of a family of receptors for the melanotropic peptides.

Cone RD, Mountjoy KG, Robbins LS, Nadeau JH, Johnson KR, Roselli-Rehfuss L, Mortrud MT. Cone RD, et al. Among authors: robbins ls. Ann N Y Acad Sci. 1993 May 31;680:342-63. doi: 10.1111/j.1749-6632.1993.tb19694.x. Ann N Y Acad Sci. 1993. PMID: 8390157 Review. No abstract available.

6

Identification of a receptor for gamma melanotropin and other proopiomelanocortin peptides in the hypothalamus and limbic system.

Roselli-Rehfuss L, Mountjoy KG, Robbins LS, Mortrud MT, Low MJ, Tatro JB, Entwistle ML, Simerly RB, Cone RD. Roselli-Rehfuss L, et al. Among authors: robbins ls. Proc Natl Acad Sci U S A. 1993 Oct 1;90(19):8856-60. doi: 10.1073/pnas.90.19.8856. Proc Natl Acad Sci U S A. 1993. PMID: 8415620 Free PMC article.

7

Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function.

Robbins LS, Nadeau JH, Johnson KR, Kelly MA, Roselli-Rehfuss L, Baack E, Mountjoy KG, Cone RD. Robbins LS, et al. Cell. 1993 Mar 26;72(6):827-34. doi: 10.1016/0092-8674(93)90572-8. Cell. 1993. PMID: 8458079

8

Identification of common polymorphisms in the coding sequence of the human MSH receptor (MCIR) with possible biological effects.

Koppula SV, Robbins LS, Lu D, Baack E, White CR Jr, Swanson NA, Cone RD. Koppula SV, et al. Among authors: robbins ls. Hum Mutat. 1997;9(1):30-6. doi: 10.1002/(SICI)1098-1004(1997)9:1<30::AID-HUMU5>3.0.CO;2-T. Hum Mutat. 1997. PMID: 8990005

9

SALL1 truncated protein expression in Townes-Brocks syndrome leads to ectopic expression of downstream genes.

Kiefer SM, Robbins L, Barina A, Zhang Z, Rauchman M. Kiefer SM, et al. Hum Mutat. 2008 Sep;29(9):1133-40. doi: 10.1002/humu.20759. Hum Mutat. 2008. PMID: 18470945

10

A mouse model of Townes-Brocks syndrome expressing a truncated mutant Sall1 protein is protected from acute kidney injury.

Hirsch S, El-Achkar T, Robbins L, Basta J, Heitmeier M, Nishinakamura R, Rauchman M. Hirsch S, et al. Am J Physiol Renal Physiol. 2015 Nov 15;309(10):F852-63. doi: 10.1152/ajprenal.00222.2015. Epub 2015 Aug 26. Am J Physiol Renal Physiol. 2015. PMID: 26311113 Free article.

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