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Summary Literature (14)
Literature for DOID 1342: congenital hypoplastic anemia


Xenbase Articles :
( Denotes literature images)
Fanconi anemia proteins are required to prevent accumulation of replication-associated DNA double-strand breaks., Sobeck A,Stone S,Costanzo V,de Graaf B,Reuter T,de Winter J,Wallisch M,Akkari Y,Olson S,Wang W,Joenje H,Christian JL,Lupardus PJ,Cimprich KA,Gautier J,Hoatlin ME, Mol Cell Biol. January 1, 2006; 26(2):1098-5549.
The Fanconi anemia gene product FANCF is a flexible adaptor protein., Léveillé F,Blom E,Medhurst AL,Bier P,Laghmani el H,Johnson M,Rooimans MA,Sobeck A,Waisfisz Q,Arwert F,Patel KJ,Hoatlin ME,Joenje H,de Winter JP, J Biol Chem. September 17, 2004; 279(38):1083-351X.
Identification, developmental expression and regulation of the Xenopus ortholog of human FANCG/XRCC9., Stone S,Sobeck A,van Kogelenberg M,de Graaf B,Joenje H,Christian J,Hoatlin ME, Genes Cells. July 1, 2007; 12(7):1356-9597.
Monoketone analogs of curcumin, a new class of Fanconi anemia pathway inhibitors., Landais I,Hiddingh S,McCarroll M,Yang C,Sun A,Turker MS,Snyder JP,Hoatlin ME, Mol Cancer. December 31, 2009; 8:1476-4598.
Fanconi anemia proteins FANCD2 and FANCI exhibit different DNA damage responses during S-phase., Sareen A,Chaudhury I,Adams N,Sobeck A, Nucleic Acids Res. September 1, 2012; 40(17):1362-4962.
FANCJ promotes DNA synthesis through G-quadruplex structures., Castillo Bosch P,Segura-Bayona S,Koole W,van Heteren JT,Dewar JM,Tijsterman M,Knipscheer P, EMBO J. November 3, 2014; 33(21):0261-4189.
Regulation of the Rev1-pol ζ complex during bypass of a DNA interstrand cross-link., Budzowska M,Graham TG,Sobeck A,Waga S,Walter JC, EMBO J. July 14, 2015; 34(14):0261-4189.
Expression of ribosomopathy genes during Xenopus tropicalis embryogenesis., Robson A,Owens ND,Baserga SJ,Khokha MK,Griffin JN, BMC Dev Biol. January 1, 2016; 16(1):1471-213X.
Fanconi-Anemia-Associated Mutations Destabilize RAD51 Filaments and Impair Replication Fork Protection., Zadorozhny K,Sannino V,Beláň O,Mlčoušková J,Špírek M,Costanzo V,Krejčí L, Cell Rep. October 10, 2017; 21(2):2211-1247.
Tissue-selective effects of nucleolar stress and rDNA damage in developmental disorders., Calo E,Gu B,Bowen ME,Aryan F,Zalc A,Liang J,Flynn RA,Swigut T,Chang HY,Attardi LD,Wysocka J, Nature. January 1, 2018; 554(7690):0143-5221.
Replication Fork Reversal during DNA Interstrand Crosslink Repair Requires CMG Unloading., Amunugama R,Willcox S,Wu RA,Abdullah UB,El-Sagheer AH,Brown T,McHugh PJ,Griffith JD,Walter JC, Cell Rep. January 1, 2018; 23(12):2211-1247.
Structural basis of the fanconi anemia-associated mutations within the FANCA and FANCG complex., Jeong E,Lee SG,Kim HS,Yang J,Shin J,Kim Y,Kim J,Schärer OD,Kim Y,Yeo JE,Kim HM,Cho Y, Nucleic Acids Res. January 1, 2020; 48(6):1362-4962.
Alcohol-derived DNA crosslinks are repaired by two distinct mechanisms., Hodskinson MR,Bolner A,Sato K,Kamimae-Lanning AN,Rooijers K,Witte M,Mahesh M,Silhan J,Petek M,Williams DM,Kind J,Chin JW,Patel KJ,Knipscheer P, Nature. January 1, 2020; 579(7800):0143-5221.
HSF2BP negatively regulates homologous recombination in DNA interstrand crosslink repair., Sato K,Brandsma I,van Rossum-Fikkert SE,Verkaik N,Oostra AB,Dorsman JC,van Gent DC,Knipscheer P,Kanaar R,Zelensky AN, Nucleic Acids Res. January 1, 2020; 48(5):1362-4962.