PubMed for id: 824604

Year	Number of Results
1984	3
1985	1
1986	1
1989	2
1990	2
1991	2
1992	2
1993	2
1994	2
1995	3
1996	1
1997	2
1998	3
1999	4
2000	7
2001	6
2002	2
2003	2
2004	1
2005	7
2006	5
2007	1
2008	14
2009	8
2010	6
2011	11
2012	10
2013	7
2014	16
2015	11
2016	14
2017	14
2018	9
2019	14
2020	9
2021	12
2022	14
2023	15
2024	2

1

Structures of FHOD1-Nesprin1/2 complexes reveal alternate binding modes for the FH3 domain of formins.

Lim SM, Cruz VE, Antoku S, Gundersen GG, Schwartz TU. Lim SM, et al. Structure. 2021 Jun 3;29(6):540-552.e5. doi: 10.1016/j.str.2020.12.013. Epub 2021 Jan 19. Structure. 2021. PMID: 33472039 Free PMC article.

2

Familial hyperaldosteronism type III a novel case and review of literature.

Pons Fernández N, Moreno F, Morata J, Moriano A, León S, De Mingo C, Zuñiga Á, Calvo F. Pons Fernández N, et al. Rev Endocr Metab Disord. 2019 Mar;20(1):27-36. doi: 10.1007/s11154-018-9481-0. Rev Endocr Metab Disord. 2019. PMID: 30569443 Review.

3

Familial hyperaldosteronism type III.

Monticone S, Tetti M, Burrello J, Buffolo F, De Giovanni R, Veglio F, Williams TA, Mulatero P. Monticone S, et al. J Hum Hypertens. 2017 Dec;31(12):776-781. doi: 10.1038/jhh.2017.34. Epub 2017 Apr 27. J Hum Hypertens. 2017. PMID: 28447626 Review.

4

Disordered zonal and cellular CYP11B2 enzyme expression in familial hyperaldosteronism type 3.

Gomez-Sanchez CE, Qi X, Gomez-Sanchez EP, Sasano H, Bohlen MO, Wisgerhof M. Gomez-Sanchez CE, et al. Mol Cell Endocrinol. 2017 Jan 5;439:74-80. doi: 10.1016/j.mce.2016.10.025. Epub 2016 Oct 25. Mol Cell Endocrinol. 2017. PMID: 27793677 Free PMC article.

5

A Novel Phenotype of Familial Hyperaldosteronism Type III: Concurrence of Aldosteronism and Cushing's Syndrome.

Tong A, Liu G, Wang F, Jiang J, Yan Z, Zhang D, Zhang Y, Cai J. Tong A, et al. J Clin Endocrinol Metab. 2016 Nov;101(11):4290-4297. doi: 10.1210/jc.2016-1504. Epub 2016 Jul 12. J Clin Endocrinol Metab. 2016. PMID: 27403928 Free PMC article.

6

Using (FH)2 and (FH)3 to Bridge the σ-Hole and the Lone Pair at P in Complexes with H2 XP, for X=CH3 , OH, H, CCH, F, Cl, NC, and CN.

Del Bene JE, Alkorta I, Elguero J. Del Bene JE, et al. Chemphyschem. 2016 May 18;17(10):1475-85. doi: 10.1002/cphc.201600048. Epub 2016 Mar 3. Chemphyschem. 2016. PMID: 26888567

7

Discordant genotype-phenotype correlation in familial hyperaldosteronism type III with KCNJ5 gene mutation: a patient report and review of the literature.

Adachi M, Muroya K, Asakura Y, Sugiyama K, Homma K, Hasegawa T. Adachi M, et al. Horm Res Paediatr. 2014;82(2):138-42. doi: 10.1159/000358197. Epub 2014 May 10. Horm Res Paediatr. 2014. PMID: 24819081 Review.

8

a Novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III.

Monticone S, Hattangady NG, Penton D, Isales CM, Edwards MA, Williams TA, Sterner C, Warth R, Mulatero P, Rainey WE. Monticone S, et al. J Clin Endocrinol Metab. 2013 Nov;98(11):E1861-5. doi: 10.1210/jc.2013-2428. Epub 2013 Sep 13. J Clin Endocrinol Metab. 2013. PMID: 24037882 Free PMC article.

9

The human formin FHOD1 contains a bipartite structure of FH3 and GTPase-binding domains required for activation.

Schulte A, Stolp B, Schönichen A, Pylypenko O, Rak A, Fackler OT, Geyer M. Schulte A, et al. Structure. 2008 Sep 10;16(9):1313-23. doi: 10.1016/j.str.2008.06.008. Structure. 2008. PMID: 18786395 Free article.

10

The multiple-wing-hairs gene encodes a novel GBD-FH3 domain-containing protein that functions both prior to and after wing hair initiation.

Yan J, Huen D, Morely T, Johnson G, Gubb D, Roote J, Adler PN. Yan J, et al. Genetics. 2008 Sep;180(1):219-28. doi: 10.1534/genetics.108.091314. Epub 2008 Aug 24. Genetics. 2008. PMID: 18723886 Free PMC article.

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