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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1995 3
1997 3
1998 5
1999 7
2000 4
2001 2
2002 10
2003 2
2004 8
2005 3
2008 1
2009 2
2010 3
2011 3
2012 2
2013 1
2014 3
2015 4
2017 1
2018 1
2019 1
2021 1
2022 1
2023 3
2024 0

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70 results

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Page 1
Nonsyndromic Retinitis Pigmentosa Overview.
Fahim AT, Daiger SP, Weleber RG. Fahim AT, et al. 2000 Aug 4 [updated 2023 Apr 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2000 Aug 4 [updated 2023 Apr 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301590 Free Books & Documents. Review.
Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease.
Agha G, Mendelson MM, Ward-Caviness CK, Joehanes R, Huan T, Gondalia R, Salfati E, Brody JA, Fiorito G, Bressler J, Chen BH, Ligthart S, Guarrera S, Colicino E, Just AC, Wahl S, Gieger C, Vandiver AR, Tanaka T, Hernandez DG, Pilling LC, Singleton AB, Sacerdote C, Krogh V, Panico S, Tumino R, Li Y, Zhang G, Stewart JD, Floyd JS, Wiggins KL, Rotter JI, Multhaup M, Bakulski K, Horvath S, Tsao PS, Absher DM, Vokonas P, Hirschhorn J, Fallin MD, Liu C, Bandinelli S, Boerwinkle E, Dehghan A, Schwartz JD, Psaty BM, Feinberg AP, Hou L, Ferrucci L, Sotoodehnia N, Matullo G, Peters A, Fornage M, Assimes TL, Whitsel EA, Levy D, Baccarelli AA. Agha G, et al. Circulation. 2019 Aug 20;140(8):645-657. doi: 10.1161/CIRCULATIONAHA.118.039357. Epub 2019 Aug 19. Circulation. 2019. PMID: 31424985 Free PMC article.
These CpGs map to genes with key roles in calcium regulation (ATP2B2, CASR, GUCA1B, HPCAL1), and genes identified in genome- and epigenome-wide studies of serum calcium (CASR), serum calcium-related risk of CHD (CASR), coronary artery calcified plaque (PTPRN2), and kidney …
These CpGs map to genes with key roles in calcium regulation (ATP2B2, CASR, GUCA1B, HPCAL1), and genes identified in genome- and epig …
Identification of hub genes correlated with diabetic retinopathy via bioinformatics methods.
Xiong JH, Chen JL, Liang JY, Zhang FF, Cheng SM. Xiong JH, et al. Eur Rev Med Pharmacol Sci. 2023 Jun;27(11):4876-4882. doi: 10.26355/eurrev_202306_32604. Eur Rev Med Pharmacol Sci. 2023. PMID: 37318461 Free article.
By constructing a protein-protein interaction (PPI) network, 10 central genes were finally identified, including CNGA1, PDE6G, RHO, ABCA4, PDE6A, PDE6B, NRL, RPE65, GUCA1B and AIPL1. CONCLUSIONS: CNGA1, PDE6G, RHO, ABCA4, PDE6A, PDE6B, NRL, RPE65, GUCA1B, and AIPL1 …
By constructing a protein-protein interaction (PPI) network, 10 central genes were finally identified, including CNGA1, PDE6G, RHO, ABCA4, P …
The uroguanylin gene (Guca1b) is linked to guanylin (Guca2) on mouse chromosome 4.
Whitaker TL, Steinbrecher KA, Copeland NG, Gilbert DJ, Jenkins NA, Cohen MB. Whitaker TL, et al. Genomics. 1997 Oct 15;45(2):348-54. doi: 10.1006/geno.1997.4942. Genomics. 1997. PMID: 9344659
We describe the cloning of the complete mouse uroguanylin gene (Guca1b) and show that Guca1b is tightly linked to the mouse guanylin gene on chromosome 4. ...
We describe the cloning of the complete mouse uroguanylin gene (Guca1b) and show that Guca1b is tightly linked to the mouse gu …
Mutation screening of the GUCA1B gene in patients with autosomal dominant cone and cone rod dystrophy.
Kitiratschky VB, Glöckner CJ, Kohl S. Kitiratschky VB, et al. Ophthalmic Genet. 2011 Sep;32(3):151-5. doi: 10.3109/13816810.2011.559650. Epub 2011 Mar 15. Ophthalmic Genet. 2011. PMID: 21405999
We therefore performed a mutation analysis of the GUCA1B gene in a clinically well characterized group of patients of European and North-American geographical origin with autosomal dominantly inherited cone dystrophy and cone rod dystrophy. ...CONCLUSION: The absence of cl …
We therefore performed a mutation analysis of the GUCA1B gene in a clinically well characterized group of patients of European and No …
A role for GCAP2 in regulating the photoresponse. Guanylyl cyclase activation and rod electrophysiology in GUCA1B knock-out mice.
Makino CL, Peshenko IV, Wen XH, Olshevskaya EV, Barrett R, Dizhoor AM. Makino CL, et al. J Biol Chem. 2008 Oct 24;283(43):29135-43. doi: 10.1074/jbc.M804445200. Epub 2008 Aug 22. J Biol Chem. 2008. PMID: 18723510 Free PMC article.
Two neuronal calcium sensors, GCAP1 and GCAP2, confer Ca(2+) sensitivity to guanylyl cyclase activity, but the importance and the contribution of each GCAP is controversial. To explore this issue, the gene GUCA1B, coding for GCAP2, was disrupted in mice, and the capacity f …
Two neuronal calcium sensors, GCAP1 and GCAP2, confer Ca(2+) sensitivity to guanylyl cyclase activity, but the importance and the contributi …
Mutations in the gene coding for guanylate cyclase-activating protein 2 (GUCA1B gene) in patients with autosomal dominant retinal dystrophies.
Sato M, Nakazawa M, Usui T, Tanimoto N, Abe H, Ohguro H. Sato M, et al. Graefes Arch Clin Exp Ophthalmol. 2005 Mar;243(3):235-42. doi: 10.1007/s00417-004-1015-7. Epub 2004 Sep 28. Graefes Arch Clin Exp Ophthalmol. 2005. PMID: 15452722
BACKGROUND: We investigated mutations in the gene coding for guanylate-cyclase activating protein 2 (GCAP2), also known as GUCA1B gene, in Japanese patients with retinitis pigmentosa (RP) and tried to identify phenotypic characteristics associated with mutations in the gen …
BACKGROUND: We investigated mutations in the gene coding for guanylate-cyclase activating protein 2 (GCAP2), also known as GUCA1B gen …
[Analysis of GUCA1B,GNGT1 and RGS9 genes in patients with retinitis pigmentosa].
Zhang QJ, Li W, Xiao XS, Li SQ, Guo XM. Zhang QJ, et al. Yi Chuan. 2002 Jan;24(1):19-21. Yi Chuan. 2002. PMID: 15901556 Chinese.
Mutation was confirmed by DNA sequencing. A T/C polymorphism was identified in exon 1 of the GUCA1B gene in 31 of the 120 probands. Heteroduplex-SSCP analysis of the GUCA1B and GNGT1 coding regions and RGS9 alternative splicing region showed no mutations in 120 pati …
Mutation was confirmed by DNA sequencing. A T/C polymorphism was identified in exon 1 of the GUCA1B gene in 31 of the 120 probands. H …
Polygenic Risk Score and Rare Variant Burden Identified by Targeted Sequencing in a Group of Patients with Pigment Epithelial Detachment in Age-Related Macular Degeneration.
Wąsowska A, Sendecki A, Boguszewska-Chachulska A, Teper S. Wąsowska A, et al. Genes (Basel). 2023 Aug 27;14(9):1707. doi: 10.3390/genes14091707. Genes (Basel). 2023. PMID: 37761846 Free PMC article.
The highest predictive value was achieved for a model consisting of six non-coding variants: rs760306 (BEST1), rs148662546 (BEST1), rs11569560 (C3), rs74600252 (GUCA1B), rs2240688 (PROM1), and rs185507582 (TCF4). The risk of PED occurrence was found to be the highest in th …
The highest predictive value was achieved for a model consisting of six non-coding variants: rs760306 (BEST1), rs148662546 (BEST1), rs115695 …
70 results