Paper Chase is a research database designed to offer abstracts of research articles published in journals that have a highly rated impact factor as determined by ISI Impact Factor and PageRank. Abstracts are organized by date, with the most recently published papers listed first. 

Paper Chase

221.

RIPK1 regulates RIPK3-MLKL-driven systemic inflammation and emergency hematopoiesis.

Cell.
Rickard JA, O'Donnell JA, Evans JM, Lalaoui N, Poh AR, Rogers T, Vince JE, Lawlor KE, Ninnis RL, Anderton H, Hall C, Spall SK, Phesse TJ, Abud HE, Cengia LH, Corbin J, Mifsud S, Di Rago L, Metcalf D, Ernst M, Dewson G, Roberts AW, Alexander WS, Murphy JM, Ekert PG, Masters SL, Vaux DL, Croker BA, Gerlic M, Silke J.
| May 22, 2014
222.

A chromatin-dependent role of the fragile X mental retardation protein FMRP in the DNA damage response.

Cell.
Alpatov R, Lesch BJ, Nakamoto-Kinoshita M, Blanco A, Chen S, Stützer A, Armache KJ, Simon MD, Xu C, Ali M, Murn J, Prisic S, Kutateladze TG, Vakoc CR, Min J, Kingston RE, Fischle W, Warren ST, Page DC, Shi Y.
| May 8, 2014
223.

Impact of circadian nuclear receptor REV-ERBα on midbrain dopamine production and mood regulation.

Cell.
Chung S, Lee EJ, Yun S, Choe HK, Park SB, Son HJ, Kim KS, Dluzen DE, Lee I, Hwang O, Son GH, Kim K.
| May 8, 2014
224.

Structurally distinct Ca(2+) signaling domains of sperm flagella orchestrate tyrosine phosphorylation and motility.

Cell.
Chung JJ, Shim SH, Everley RA, Gygi SP, Zhuang X, Clapham DE.
| May 8, 2014
225.

Tic-TACs: refreshing hair growth.

Cell.
Kalaitzidis D, Scadden DT.
| May 8, 2014
226.

Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies.

Nat. Med.
Wang G, McCain ML, Yang L, He A, Pasqualini FS, Agarwal A, Yuan H, Jiang D, Zhang D, Zangi L, Geva J, Roberts AE, Ma Q, Ding J, Chen J, Wang DZ, Li K, Wang J, Wanders RJ, Kulik W, Vaz FM, Laflamme MA, Murry CE, Chien KR, Kelley RI, Church GM, Parker KK, Pu WT.
| 05 11, 2014
227.

Rescue of Hippo coactivator YAP1 triggers DNA damage-induced apoptosis in hematological cancers.

Nat. Med.
Cottini F, Hideshima T, Xu C, Sattler M, Dori M, Agnelli L, ten Hacken E, Bertilaccio MT, Antonini E, Neri A, Ponzoni M, Marcatti M, Richardson PG, Carrasco R, Kimmelman AC, Wong KK, Caligaris-Cappio F, Blandino G, Kuehl WM, Anderson KC, Tonon G.
| 05 11, 2014
228.

Sound strategies for hearing restoration.

Science.
Géléoc GS, Holt JR.
| May 9, 2014
229.

Evolution of the primate trypanolytic factor APOL1.

Proc. Natl. Acad. Sci. U.S.A.
Thomson R, Genovese G, Canon C, Kovacsics D, Higgins MK, Carrington M, Winkler CA, Kopp J, Rotimi C, Adeyemo A, Doumatey A, Ayodo G, Alper SL, Pollak MR, Friedman DJ, Raper J.
| May 20, 2014
230.

The axes of access--improving care for patients with disabilities.

N. Engl. J. Med.
Lagu T, Iezzoni LI, Lindenauer PK.
| May 8, 2014
231.

Synthetic biology: Engineering explored.

Nature.
Silver PA, Way JC, Arnold FH, Meyerowitz JT.
| May 8, 2014
232.

Antibiotics induce redox-related physiological alterations as part of their lethality.

Proc. Natl. Acad. Sci. U.S.A.
Dwyer DJ, Belenky PA, Yang JH, MacDonald IC, Martell JD, Takahashi N, Chan CT, Lobritz MA, Braff D, Schwarz EG, Ye JD, Pati M, Vercruysse M, Ralifo PS, Allison KR, Khalil AS, Ting AY, Walker GC, Collins JJ.
| May 20, 2014
233.

Discharges against medical advice.

JAMA.
Querques J, Kontos N, Freudenreich O.
| May 7, 2014
234.

Cholesterol testing among children and adolescents during health visits.

JAMA.
Vinci SR, Rifas-Shiman SL, Cheng JK, Mannix RC, Gillman MW, de Ferranti SD.
| May 7, 2014
235.

Idiopathic short stature: a clinical review.

JAMA.
Cohen LE.
| May 7, 2014
236.

Preventing health care-associated harm in children.

JAMA.
Walsh KE, Bundy DG, Landrigan CP.
| May 7, 2014
237.

Pan-cancer genetic analysis identifies PARK2 as a master regulator of G1/S cyclins.

Nat. Genet.
Gong Y, Zack TI, Morris LG, Lin K, Hukkelhoven E, Raheja R, Tan IL, Turcan S, Veeriah S, Meng S, Viale A, Schumacher SE, Palmedo P, Beroukhim R, Chan TA.
| 05 04, 2014
238.

A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations.

Nat. Genet.
Kohsaka S, Shukla N, Ameur N, Ito T, Ng CK, Wang L, Lim D, Marchetti A, Viale A, Pirun M, Socci ND, Qin LX, Sciot R, Bridge J, Singer S, Meyers P, Wexler LH, Barr FG, Dogan S, Fletcher JA, Reis-Filho JS, Ladanyi M.
| 05 04, 2014
239.

Dystrophin is a tumor suppressor in human cancers with myogenic programs.

Nat. Genet.
Wang Y, Marino-Enriquez A, Bennett RR, Zhu M, Shen Y, Eilers G, Lee JC, Henze J, Fletcher BS, Gu Z, Fox EA, Antonescu CR, Fletcher CD, Guo X, Raut CP, Demetri GD, van de Rijn M, Ordog T, Kunkel LM, Fletcher JA.
| 05 04, 2014
240.

Polarization of the effects of autoimmune and neurodegenerative risk alleles in leukocytes.

Science.
Raj T, Rothamel K, Mostafavi S, Ye C, Lee MN, Replogle JM, Feng T, Lee M, Asinovski N, Frohlich I, Imboywa S, Von Korff A, Okada Y, Patsopoulos NA, Davis S, McCabe C, Paik HI, Srivastava GP, Raychaudhuri S, Hafler DA, Koller D, Regev A, Hacohen N, Mathis D, Benoist C, Stranger BE, De Jager PL.
| May 2, 2014