Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1995 | 1 |
1997 | 1 |
2003 | 1 |
2013 | 1 |
2015 | 1 |
2020 | 1 |
2021 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 3021
7 results
Results by year
Filters applied: . Clear all
Page 1
De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities.
NPJ Genom Med. 2021 Dec 7;6(1):104. doi: 10.1038/s41525-021-00268-8.
NPJ Genom Med. 2021.
PMID: 34876591
Free PMC article.
Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients.
Bryant L, Li D, Cox SG, Marchione D, Joiner EF, Wilson K, Janssen K, Lee P, March ME, Nair D, Sherr E, Fregeau B, Wierenga KJ, Wadley A, Mancini GMS, Powell-Hamilton N, van de Kamp J, Grebe T, Dean J, Ross A, Crawford HP, Powis Z, Cho MT, Willing MC, Manwaring L, Schot R, Nava C, Afenjar A, Lessel D, Wagner M, Klopstock T, Winkelmann J, Catarino CB, Retterer K, Schuette JL, Innis JW, Pizzino A, Lüttgen S, Denecke J, Strom TM, Monaghan KG; DDD Study; Yuan ZF, Dubbs H, Bend R, Lee JA, Lyons MJ, Hoefele J, Günthner R, Reutter H, Keren B, Radtke K, Sherbini O, Mrokse C, Helbig KL, Odent S, Cogne B, Mercier S, Bezieau S, Besnard T, Kury S, Redon R, Reinson K, Wojcik MH, Õunap K, Ilves P, Innes AM, Kernohan KD; Care4Rare Canada Consortium; Costain G, Meyn MS, Chitayat D, Zackai E, Lehman A, Kitson H; CAUSES Study; Martin MG, Martinez-Agosto JA; Undiagnosed Diseases Network; Nelson SF, Palmer CGS, Papp JC, Parker NH, Sinsheimer JS, Vilain E, Wan J, Yoon AJ, Zheng A, Brimble E, Ferrero GB, Radio FC, Carli D, Barresi S, Brusco A, Tartaglia M, Thomas JM, Umana L, Weiss MM, Gotway G, Stuurman KE, Thompson ML, McWalter K, Stumpel CTRM, Stevens SJC, Stegmann APA, Tveten K, Vøllo A, Prescott T,…
See abstract for full author list ➔
Bryant L, et al.
Sci Adv. 2020 Dec 2;6(49):eabc9207. doi: 10.1126/sciadv.abc9207. Print 2020 Dec.
Sci Adv. 2020.
PMID: 33268356
Free PMC article.
Item in Clipboard
Histone H3.3 maintains genome integrity during mammalian development.
Jang CW, Shibata Y, Starmer J, Yee D, Magnuson T.
Jang CW, et al.
Genes Dev. 2015 Jul 1;29(13):1377-92. doi: 10.1101/gad.264150.115.
Genes Dev. 2015.
PMID: 26159997
Free PMC article.
Item in Clipboard
Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone.
Behjati S, Tarpey PS, Presneau N, Scheipl S, Pillay N, Van Loo P, Wedge DC, Cooke SL, Gundem G, Davies H, Nik-Zainal S, Martin S, McLaren S, Goodie V, Robinson B, Butler A, Teague JW, Halai D, Khatri B, Myklebost O, Baumhoer D, Jundt G, Hamoudi R, Tirabosco R, Amary MF, Futreal PA, Stratton MR, Campbell PJ, Flanagan AM.
Behjati S, et al.
Nat Genet. 2013 Dec;45(12):1479-82. doi: 10.1038/ng.2814. Epub 2013 Oct 27.
Nat Genet. 2013.
PMID: 24162739
Free PMC article.
Item in Clipboard
Differential expression of human replacement and cell cycle dependent H3 histone genes.
Frank D, Doenecke D, Albig W.
Frank D, et al.
Gene. 2003 Jul 17;312:135-43. doi: 10.1016/s0378-1119(03)00609-7.
Gene. 2003.
PMID: 12909349
Item in Clipboard
Transcriptional regulation of the human replacement histone gene H3.3B.
Witt O, Albig W, Doenecke D.
Witt O, et al.
FEBS Lett. 1997 May 26;408(3):255-60. doi: 10.1016/s0014-5793(97)00436-5.
FEBS Lett. 1997.
PMID: 9188772
Free article.
Item in Clipboard
The human replacement histone H3.3B gene (H3F3B).
Albig W, Bramlage B, Gruber K, Klobeck HG, Kunz J, Doenecke D.
Albig W, et al.
Genomics. 1995 Nov 20;30(2):264-72. doi: 10.1006/geno.1995.9878.
Genomics. 1995.
PMID: 8586426
Item in Clipboard
Cite
Cite