144 related articles for article (PubMed ID: 37547463)
1. A self-repair history: compensatory effect of a
Persico I; Fontana G; Faleschini M; Zanchetta ME; Ammeti D; Cappelli E; Corsolini F; Mosa C; Guarina A; Bogliolo M; Surrallés J; Dufour C; Farruggia P; Savoia A; Bottega R
Front Genet; 2023; 14():1209138. PubMed ID: 37547463
[No Abstract] [Full Text] [Related]
2. Erratum: A self-repair history: compensatory effect of a
Frontiers Production Office
Front Genet; 2023; 14():1293778. PubMed ID: 37799138
[TBL] [Abstract][Full Text] [Related]
3. Bone Marrow Mesenchymal Stem Cells Carrying FANCD2 Mutation Differ from the Other Fanconi Anemia Complementation Groups in Terms of TGF-β1 Production.
Cagnan I; Gunel-Ozcan A; Aerts-Kaya F; Ameziane N; Kuskonmaz B; Dorsman J; Gumruk F; Uckan D
Stem Cell Rev Rep; 2018 Jun; 14(3):425-437. PubMed ID: 29247345
[TBL] [Abstract][Full Text] [Related]
4. Esophageal cancer as initial presentation of Fanconi anemia in patients with a hypomorphic
Lach FP; Singh S; Rickman KA; Ruiz PD; Noonan RJ; Hymes KB; DeLacure MD; Kennedy JA; Chandrasekharappa SC; Smogorzewska A
Cold Spring Harb Mol Case Stud; 2020 Dec; 6(6):. PubMed ID: 33172906
[TBL] [Abstract][Full Text] [Related]
5. Phenotype reversion as "natural gene therapy" in Fanconi anemia by a gene conversion event.
Persico I; Fiscarelli I; Pelle A; Faleschini M; Pasini B; Savoia A; Bottega R
Front Genet; 2023; 14():1240758. PubMed ID: 37790699
[TBL] [Abstract][Full Text] [Related]
6. Heterogeneous activation of the Fanconi anemia pathway by patient-derived FANCA mutants.
Adachi D; Oda T; Yagasaki H; Nakasato K; Taniguchi T; D'Andrea AD; Asano S; Yamashita T
Hum Mol Genet; 2002 Dec; 11(25):3125-34. PubMed ID: 12444097
[TBL] [Abstract][Full Text] [Related]
7. Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50.
Chandrasekharappa SC; Chinn SB; Donovan FX; Chowdhury NI; Kamat A; Adeyemo AA; Thomas JW; Vemulapalli M; Hussey CS; Reid HH; Mullikin JC; Wei Q; Sturgis EM
Cancer; 2017 Oct; 123(20):3943-3954. PubMed ID: 28678401
[TBL] [Abstract][Full Text] [Related]
8. Function of the Fanconi anemia pathway in Fanconi anemia complementation group F and D1 cells.
Siddique MA; Nakanishi K; Taniguchi T; Grompe M; D'Andrea AD
Exp Hematol; 2001 Dec; 29(12):1448-55. PubMed ID: 11750104
[TBL] [Abstract][Full Text] [Related]
9. The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC.
Taniguchi T; D'Andrea AD
Blood; 2002 Oct; 100(7):2457-62. PubMed ID: 12239156
[TBL] [Abstract][Full Text] [Related]
10. Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variant.
Savino M; Borriello A; D'Apolito M; Criscuolo M; Del Vecchio M; Bianco AM; Di Perna M; Calzone R; Nobili B; Zatterale A; Zelante L; Joenje H; Della Ragione F; Savoia A
Hum Mutat; 2003 Oct; 22(4):338-9. PubMed ID: 12955722
[TBL] [Abstract][Full Text] [Related]
11. Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction.
Gross M; Hanenberg H; Lobitz S; Friedl R; Herterich S; Dietrich R; Gruhn B; Schindler D; Hoehn H
Cytogenet Genome Res; 2002; 98(2-3):126-35. PubMed ID: 12697994
[TBL] [Abstract][Full Text] [Related]
12. An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis.
Yamamura T; Nozu K; Miyoshi Y; Nakanishi K; Fujimura J; Horinouchi T; Minamikawa S; Mori N; Fujimaru R; Nakanishi K; Ninchoji T; Kaito H; Mariko TI; Morioka I; Matsuo M; Iijima K
BMC Nephrol; 2017 Dec; 18(1):353. PubMed ID: 29202719
[TBL] [Abstract][Full Text] [Related]
13. Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey.
Toksoy G; Uludağ Alkaya D; Bagirova G; Avcı Ş; Aghayev A; Günes N; Altunoğlu U; Alanay Y; Başaran S; Berkay EG; Karaman B; Celkan TT; Apak H; Kayserili H; Tüysüz B; Uyguner ZO
Mol Syndromol; 2020 Nov; 11(4):183-196. PubMed ID: 33224012
[TBL] [Abstract][Full Text] [Related]
14. The Fanconi anemia proteins FANCD2 and FANCJ interact and regulate each other's chromatin localization.
Chen X; Wilson JB; McChesney P; Williams SA; Kwon Y; Longerich S; Marriott AS; Sung P; Jones NJ; Kupfer GM
J Biol Chem; 2014 Sep; 289(37):25774-82. PubMed ID: 25070891
[TBL] [Abstract][Full Text] [Related]
15. Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies.
Bogliolo M; Pujol R; Aza-Carmona M; Muñoz-Subirana N; Rodriguez-Santiago B; Casado JA; Rio P; Bauser C; Reina-Castillón J; Lopez-Sanchez M; Gonzalez-Quereda L; Gallano P; Catalá A; Ruiz-Llobet A; Badell I; Diaz-Heredia C; Hladun R; Senent L; Argiles B; Bergua Burgues JM; Bañez F; Arrizabalaga B; López Almaraz R; Lopez M; Figuera Á; Molinés A; Pérez de Soto I; Hernando I; Muñoz JA; Del Rosario Marin M; Balmaña J; Stjepanovic N; Carrasco E; Cuesta I; Cosuelo JM; Regueiro A; Moraleda Jimenez J; Galera-Miñarro AM; Rosiñol L; Carrió A; Beléndez-Bieler C; Escudero Soto A; Cela E; de la Mata G; Fernández-Delgado R; Garcia-Pardos MC; Sáez-Villaverde R; Barragaño M; Portugal R; Lendinez F; Hernadez I; Vagace JM; Tapia M; Nieto J; Garcia M; Gonzalez M; Vicho C; Galvez E; Valiente A; Antelo ML; Ancliff P; Garcia F; Dopazo J; Sevilla J; Paprotka T; Pérez-Jurado LA; Bueren J; Surralles J
J Med Genet; 2020 Apr; 57(4):258-268. PubMed ID: 31586946
[TBL] [Abstract][Full Text] [Related]
16. Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs.
Tamary H; Dgany O; Toledano H; Shalev Z; Krasnov T; Shalmon L; Schechter T; Bercovich D; Attias D; Laor R; Koren A; Yaniv I
Eur J Haematol; 2004 May; 72(5):330-5. PubMed ID: 15059067
[TBL] [Abstract][Full Text] [Related]
17. Functional analysis of Fanconi anemia mutations in China.
Li N; Ding L; Li B; Wang J; D'Andrea AD; Chen J
Exp Hematol; 2018 Oct; 66():32-41.e8. PubMed ID: 30031030
[TBL] [Abstract][Full Text] [Related]
18. Genetic analysis of a Fanconi anemia case revealed the presence of FANCF mutation (exon 1;469>C-T) with implications to develop acute myeloid leukemia.
Behera CK; Gyandeep G; Mishra R; Mohanty RP; Pal A; Behera J; Samal S; Das B
Mol Biol Rep; 2023 Jan; 50(1):931-936. PubMed ID: 36369330
[TBL] [Abstract][Full Text] [Related]
19. Usefulness of functional splicing analysis to confirm precise disease pathogenesis in Diamond-Blackfan anemia caused by intronic variants in
Takafuji S; Mori T; Nishimura N; Yamamoto N; Uemura S; Nozu K; Terui K; Toki T; Ito E; Muramatsu H; Takahashi Y; Matsuo M; Yamamura T; Iijima K
Pediatr Hematol Oncol; 2021 Sep; 38(6):515-527. PubMed ID: 33622161
[TBL] [Abstract][Full Text] [Related]
20. Evidence for subcomplexes in the Fanconi anemia pathway.
Medhurst AL; Laghmani el H; Steltenpool J; Ferrer M; Fontaine C; de Groot J; Rooimans MA; Scheper RJ; Meetei AR; Wang W; Joenje H; de Winter JP
Blood; 2006 Sep; 108(6):2072-80. PubMed ID: 16720839
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
