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1,625 results
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Offspring to Parent LDLT: Narrowing the Gap Between Theory and Evidence.
Choudhury RA, Yoeli D, Dagan A, Yaffe H, Moore HB, Conzen KD, Adams M, Wachs M, Pomposelli JJ, Pomfret EA, Nydam TL. Choudhury RA, et al. Among authors: moore hb. Transplantation. 2020 Oct;104(10):e307. doi: 10.1097/TP.0000000000003352. Transplantation. 2020. PMID: 32969991 No abstract available.
Vulnerable and Resilient Phenotypes in a Mouse Model of Anorexia Nervosa.
Beeler JA, Mourra D, Zanca RM, Kalmbach A, Gellman C, Klein BY, Ravenelle R, Serrano P, Moore H, Rayport S, Mingote S, Burghardt NS. Beeler JA, et al. Among authors: moore h. Biol Psychiatry. 2020 Jul 16:S0006-3223(20)31744-3. doi: 10.1016/j.biopsych.2020.06.030. Online ahead of print. Biol Psychiatry. 2020. PMID: 32950210
GMP-grade neural progenitor derivation and differentiation from clinical-grade human embryonic stem cells.
Vitillo L, Durance C, Hewitt Z, Moore H, Smith A, Vallier L. Vitillo L, et al. Among authors: moore h. Stem Cell Res Ther. 2020 Sep 18;11(1):406. doi: 10.1186/s13287-020-01915-0. Stem Cell Res Ther. 2020. PMID: 32948237 Free article.
Orthopaedic Injuries Associated With Cell Phone Use Resulting in Emergency Department Visits: A 20-year Analysis.
Moore HG, Halperin SJ, Berson ER, Burroughs PJ, Paskhover B, Grauer JN. Moore HG, et al. J Am Acad Orthop Surg. 2020 Sep 17. doi: 10.5435/JAAOS-D-20-00639. Online ahead of print. J Am Acad Orthop Surg. 2020. PMID: 32947349
Plasmin TEG Rapidly Identifies Trauma Patients at Risk for Massive Transfusion, Mortality and Hyperfibrinolysis: A Diagnostic Tool to Resolve an International Debate on TXA?
Barrett CD, Moore HB, Vigneshwar N, Dhara S, Chandler J, Chapman MP, Sauaia A, Moore EE, Yaffe MB. Barrett CD, et al. Among authors: moore hb. J Trauma Acute Care Surg. 2020 Sep 9. doi: 10.1097/TA.0000000000002941. Online ahead of print. J Trauma Acute Care Surg. 2020. PMID: 32925578
A Quantitative Proteome Map of the Human Body.
Jiang L, Wang M, Lin S, Jian R, Li X, Chan J, Dong G, Fang H, Robinson AE; GTEx Consortium, Snyder MP. Jiang L, et al. Cell. 2020 Sep 5:S0092-8674(20)31078-3. doi: 10.1016/j.cell.2020.08.036. Online ahead of print. Cell. 2020. PMID: 32916130
A vast resource of allelic expression data spanning human tissues.
Castel SE, Aguet F, Mohammadi P; GTEx Consortium, Ardlie KG, Lappalainen T. Castel SE, et al. Genome Biol. 2020 Sep 11;21(1):234. doi: 10.1186/s13059-020-02122-z. Genome Biol. 2020. PMID: 32912332 Free PMC article.
De Novo Variants in LMNB1 Cause Pronounced Syndromic Microcephaly and Disruption of Nuclear Envelope Integrity.
Cristofoli F, Moss T, Moore HW, Devriendt K, Flanagan-Steet H, May M, Jones J, Roelens F, Fons C, Fernandez A, Martorell L, Selicorni A, Maitz S, Vitiello G, Van der Hoeven G, Skinner SA, Bollen M, Vermeesch JR, Steet R, Van Esch H. Cristofoli F, et al. Among authors: moore hw. Am J Hum Genet. 2020 Sep 1:S0002-9297(20)30284-6. doi: 10.1016/j.ajhg.2020.08.015. Online ahead of print. Am J Hum Genet. 2020. PMID: 32910914
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