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Items: 1 to 20 of 2990427

1.

Distinct Genetic Risk Profile of the Rapidly Progressing Diffuse-Trickling Subtype of Geographic Atrophy in Age-Related Macular Degeneration (AMD).

Fleckenstein M, Grassmann F, Lindner M, Pfau M, Czauderna J, Strunz T, von Strachwitz C, Schmitz-Valckenberg S, Holz FG, Weber BH.

Invest Ophthalmol Vis Sci. 2016 May 1;57(6):2463-2471. doi: 10.1167/iovs.15-18593.

PMID:
27149696
2.

Prediagnostic aspirin use and mortality in women with stage I to III breast cancer: A cohort study in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial.

Bradley MC, Black A, Freedman AN, Barron TI.

Cancer. 2016 May 3. doi: 10.1002/cncr.30004. [Epub ahead of print]

PMID:
27149646
3.

Ehlers-Danlos syndrome(s) mimicking child abuse: Is there an impact on clinical practice?

Castori M.

Am J Med Genet A. 2016 May 5. doi: 10.1002/ajmg.a.37733. [Epub ahead of print] No abstract available.

PMID:
27149643
4.

Rapid clinical deterioration in an individual with Down syndrome.

Jacobs J, Schwartz A, McDougle CJ, Skotko BG.

Am J Med Genet A. 2016 May 5. doi: 10.1002/ajmg.a.37674. [Epub ahead of print]

PMID:
27149638
5.

Mapping of Mycobacterium tuberculosis Complex Genetic Diversity Profiles in Tanzania and Other African Countries.

Mbugi EV, Katale BZ, Streicher EM, Keyyu JD, Kendall SL, Dockrell HM, Michel AL, Rweyemamu MM, Warren RM, Matee MI, van Helden PD, Couvin D, Rastogi N.

PLoS One. 2016 May 5;11(5):e0154571. doi: 10.1371/journal.pone.0154571. eCollection 2016.

PMID:
27149626
6.

Influenza Virus Affects Intestinal Microbiota and Secondary Salmonella Infection in the Gut through Type I Interferons.

Deriu E, Boxx GM, He X, Pan C, Benavidez SD, Cen L, Rozengurt N, Shi W, Cheng G.

PLoS Pathog. 2016 May 5;12(5):e1005572. doi: 10.1371/journal.ppat.1005572. eCollection 2016 May.

PMID:
27149619
7.

Exploiting Genetic Interference for Antiviral Therapy.

Tanner EJ, Kirkegaard KA, Weinberger LS.

PLoS Genet. 2016 May 5;12(5):e1005986. doi: 10.1371/journal.pgen.1005986. eCollection 2016 May. Review.

PMID:
27149616
8.

Folate status, regulatory T cells and MTHFR C677T polymorphism study in allergic children.

Socha-Banasiak A, Kamer B, Gach A, Wysocka U, Jakubowski L, Głowacka E, Czkwianianc E.

Adv Med Sci. 2016 Apr 8;61(2):300-305. doi: 10.1016/j.advms.2016.03.010. [Epub ahead of print]

PMID:
27149557
9.

Using CRISPR/Cas to study gene function and model disease in vivo.

Tschaharganeh DF, Lowe SW, Garippa RJ, Livshits G.

FEBS J. 2016 May 5. doi: 10.1111/febs.13750. [Epub ahead of print]

PMID:
27149548
10.

Adolescents' preferences regarding disclosure of incidental findings in genomic sequencing that are not medically actionable in childhood.

Hufnagel SB, Martin LJ, Cassedy A, Hopkin RJ, Antommaria AH.

Am J Med Genet A. 2016 May 5. doi: 10.1002/ajmg.a.37730. [Epub ahead of print]

PMID:
27149544
11.

Fungal Genomics Challenges the Dogma of Name-Based Biosecurity.

McTaggart AR, van der Nest MA, Steenkamp ET, Roux J, Slippers B, Shuey LS, Wingfield MJ, Drenth A.

PLoS Pathog. 2016 May 5;12(5):e1005475. doi: 10.1371/journal.ppat.1005475. eCollection 2016 May. No abstract available.

PMID:
27149511
12.

Loss of MAPK Pathway Activation in Post-Mitotic Retinal Cells as Mechanism in MEK Inhibition-Related Retinopathy in Cancer Patients.

van Dijk EH, Duits DE, Versluis M, Luyten GP, Bergen AA, Kapiteijn EW, de Lange MJ, Boon CJ, van der Velden PA.

Medicine (Baltimore). 2016 May;95(18):e3457.

PMID:
27149444
13.

A Case of T-cell Acute Lymphoblastic Leukemia Relapsed As Myeloid Acute Leukemia.

Paganin M, Buldini B, Germano G, Seganfreddo E, Meglio AD, Magrin E, Grillo F, Pigazzi M, Rizzari C, Cazzaniga G, Khiabanian H, Palomero T, Rabadan R, Ferrando AA, Basso G.

Pediatr Blood Cancer. 2016 May 3. doi: 10.1002/pbc.26054. [Epub ahead of print]

PMID:
27149388
14.

Secretome Profiling of Periodontal Ligament from Deciduous and Permanent Teeth Reveals a Distinct Expression Pattern of Laminin Chains.

Giovani PA, Salmon CR, Martins L, Paes Leme AF, Rebouças P, Puppin Rontani RM, Mofatto LS, Sallum EA, Nociti FH Jr, Kantovitz KR.

PLoS One. 2016 May 5;11(5):e0154957. doi: 10.1371/journal.pone.0154957. eCollection 2016.

PMID:
27149379
15.

Further delineation of FKBP14-related Ehlers-Danlos syndrome: A patient with early vascular complications and non-progressive kyphoscoliosis, and literature review.

Dordoni C, Ciaccio C, Venturini M, Calzavara-Pinton P, Ritelli M, Colombi M.

Am J Med Genet A. 2016 May 5. doi: 10.1002/ajmg.a.37728. [Epub ahead of print]

PMID:
27149304
16.

Mechanisms of the Maternal Exposome and Implications for Health Outcomes.

Wright ML, Starkweather AR, York TP.

ANS Adv Nurs Sci. 2016 Apr-Jun;39(2):E17-E30.

PMID:
27149232
17.

First clinical report of an infant with microcephaly and CASC5 mutations.

Zarate YA, Kaylor JA, Bosanko K, Lau S, Vargas J, Gao H.

Am J Med Genet A. 2016 May 5. doi: 10.1002/ajmg.a.37726. [Epub ahead of print] No abstract available.

PMID:
27149178
18.

Single cell stable isotope probing in microbiology using Raman microspectroscopy.

Wang Y, Huang WE, Cui L, Wagner M.

Curr Opin Biotechnol. 2016 May 2;41:34-42. doi: 10.1016/j.copbio.2016.04.018. [Epub ahead of print] Review.

PMID:
27149160
19.

Neuropsychiatric symptom modeling in male and female C57BL/6J mice following experimental traumatic brain injury.

Tucker LT, Burke JF, Fu AH, McCabe JT.

J Neurotrauma. 2016 May 5. [Epub ahead of print]

PMID:
27149139
20.

Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure.

Smith JG, Felix JF, Morrison AC, Kalogeropoulos A, Trompet S, Wilk JB, Gidlöf O, Wang X, Morley M, Mendelson M, Joehanes R, Ligthart S, Shan X, Bis JC, Wang YA, Sjögren M, Ngwa J, Brandimarto J, Stott DJ, Aguilar D, Rice KM, Sesso HD, Demissie S, Buckley BM, Taylor KD, Ford I, Yao C, Liu C; CHARGE-SCD consortium; EchoGen consortium; QT-IGC consortium; CHARGE-QRS consortium, Sotoodehnia N, van der Harst P, Stricker BH, Kritchevsky SB, Liu Y, Gaziano JM, Hofman A, Moravec CS, Uitterlinden AG, Kellis M, van Meurs JB, Margulies KB, Dehghan A, Levy D, Olde B, Psaty BM, Cupples LA, Jukema JW, Djousse L, Franco OH, Boerwinkle E, Boyer LA, Newton-Cheh C, Butler J, Vasan RS, Cappola TP, Smith NL.

PLoS Genet. 2016 May 5;12(5):e1006034. doi: 10.1371/journal.pgen.1006034. eCollection 2016 May.

PMID:
27149122
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