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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1994 | 1 |
1998 | 1 |
1999 | 1 |
2000 | 2 |
2001 | 1 |
2002 | 1 |
2003 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 338577
7 results
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Page 1
Cold-induced sweating syndrome is caused by mutations in the CRLF1 gene.
Am J Hum Genet. 2003 Feb;72(2):375-83. doi: 10.1086/346120. Epub 2002 Dec 31.
Am J Hum Genet. 2003.
PMID: 12509788
Free PMC article.
Ciliary neurotrophic factor activates leptin-like pathways and reduces body fat, without cachexia or rebound weight gain, even in leptin-resistant obesity.
Lambert PD, Anderson KD, Sleeman MW, Wong V, Tan J, Hijarunguru A, Corcoran TL, Murray JD, Thabet KE, Yancopoulos GD, Wiegand SJ.
Lambert PD, et al.
Proc Natl Acad Sci U S A. 2001 Apr 10;98(8):4652-7. doi: 10.1073/pnas.061034298. Epub 2001 Mar 20.
Proc Natl Acad Sci U S A. 2001.
PMID: 11259650
Free PMC article.
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CLF associates with CLC to form a functional heteromeric ligand for the CNTF receptor complex.
Elson GC, Lelièvre E, Guillet C, Chevalier S, Plun-Favreau H, Froger J, Suard I, de Coignac AB, Delneste Y, Bonnefoy JY, Gauchat JF, Gascan H.
Elson GC, et al.
Nat Neurosci. 2000 Sep;3(9):867-72. doi: 10.1038/78765.
Nat Neurosci. 2000.
PMID: 10966616
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CNTF II, I presume?
Lesser SS, Lo DC.
Lesser SS, et al.
Nat Neurosci. 2000 Sep;3(9):851-2. doi: 10.1038/78738.
Nat Neurosci. 2000.
PMID: 10966608
Review.
No abstract available.
Item in Clipboard
Suckling defect in mice lacking the soluble haemopoietin receptor NR6.
Alexander WS, Rakar S, Robb L, Farley A, Willson TA, Zhang JG, Hartley L, Kikuchi Y, Kojima T, Nomura H, Hasegawa M, Maeda M, Fabri L, Jachno K, Nash A, Metcalf D, Nicola NA, Hilton DJ.
Alexander WS, et al.
Curr Biol. 1999 Jun 3;9(11):605-8. doi: 10.1016/s0960-9822(99)80266-8.
Curr Biol. 1999.
PMID: 10359701
Free article.
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Cytokine-like factor-1, a novel soluble protein, shares homology with members of the cytokine type I receptor family.
Elson GC, Graber P, Losberger C, Herren S, Gretener D, Menoud LN, Wells TN, Kosco-Vilbois MH, Gauchat JF.
Elson GC, et al.
J Immunol. 1998 Aug 1;161(3):1371-9.
J Immunol. 1998.
PMID: 9686600
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A null mutation in the human CNTF gene is not causally related to neurological diseases.
Takahashi R, Yokoji H, Misawa H, Hayashi M, Hu J, Deguchi T.
Takahashi R, et al.
Nat Genet. 1994 May;7(1):79-84. doi: 10.1038/ng0594-79.
Nat Genet. 1994.
PMID: 8075647
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