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Crystallographic Detection of the Spin State in FeIII Complexes.
Kelly CT, Griffin M, Esien K, Felton S, Müller-Bunz H, Morgan GG. Kelly CT, et al. Among authors: griffin m. Cryst Growth Des. 2022 Nov 2;22(11):6429-6439. doi: 10.1021/acs.cgd.2c00468. Epub 2022 Oct 17. Cryst Growth Des. 2022. PMID: 36345384 Free PMC article.
A symmetry-breaking spin-state transition in iron(III).
Griffin M, Shakespeare S, Shepherd HJ, Harding CJ, Létard JF, Desplanches C, Goeta AE, Howard JA, Powell AK, Mereacre V, Garcia Y, Naik AD, Müller-Bunz H, Morgan GG. Griffin M, et al. Angew Chem Int Ed Engl. 2011 Jan 24;50(4):896-900. doi: 10.1002/anie.201005545. Epub 2010 Nov 12. Angew Chem Int Ed Engl. 2011. PMID: 21246686 No abstract available.
Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016-2023).
Lin AE, Scimone ER, Thom RP, Balaguru D, Kinane TB, Moschovis PP, Cohen MS, Tan W, Hague CD, Dannheim K, Levitsky LL, Lilly E, DiGiacomo DV, Masse KM, Kadzielski SM, Zar-Kessler CA, Ginns LC, Neumeyer AM, Colvin MK, Elder JS, Learn CP, Mou H, Weagle KM, Buch KA, Butler WE, Alhadid K, Musolino PL, Sultana S, Bandyopadhyay D, Rapalino O, Peacock ZS, Chou EL, Heidary G, Dorfman AT, Morris SA, Bergin JD, Rayment JH, Schimmenti LA, Lindsay ME; MGH Myhre Syndrome Study Group. Lin AE, et al. Am J Med Genet A. 2024 May 23:e63638. doi: 10.1002/ajmg.a.63638. Online ahead of print. Am J Med Genet A. 2024. PMID: 38779990
Investigation of health inequities in maternal and neonatal outcomes of patients with placenta accreta spectrum: a multicenter study.
Cohen A, Lambert C, Yanik M, Nathan L, Rosenberg HM, Tavella N, Bianco A, Futterman I, Haberman S, Griffin MM, Limaye M, Owens T, Brustman L, Wu H, Dar P, Jessel RH, Doulaveris G. Cohen A, et al. Among authors: griffin mm. Am J Obstet Gynecol MFM. 2024 May 16:101386. doi: 10.1016/j.ajogmf.2024.101386. Online ahead of print. Am J Obstet Gynecol MFM. 2024. PMID: 38761887
De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features.
Mullegama SV, Kiernan KA, Torti E, Pavlovsky E, Tilton N, Sekula A, Gao H, Alaimo JT, Engleman K, Rush ET, Blocker K, Dipple KM, Fettig VM, Hare H, Glass I, Grange DK, Griffin M, Phornphutkul C, Massingham L, Mehta L, Miller DE, Thies J, Merritt JL 2nd, Muller E 2nd, Osmond M, Sawyer SL, Slaugh R, Hickey RE, Wolf B; Care4Rare Canada Consortium; Undiagnosed Diseases Network; Choudhary S, Simonović M, Zhang Y, Palculict TB, Telegrafi A, Carere DA, Wentzensen IM, Morrow MM, Monaghan KG, Juusola J, Yang J. Mullegama SV, et al. Among authors: griffin m. Am J Hum Genet. 2024 May 14:S0002-9297(24)00167-8. doi: 10.1016/j.ajhg.2024.05.004. Online ahead of print. Am J Hum Genet. 2024. PMID: 38749428 No abstract available.
Understanding Tendon Fibroblast Biology and Heterogeneity.
DiIorio SE, Young B, Parker JB, Griffin MF, Longaker MT. DiIorio SE, et al. Among authors: griffin mf. Biomedicines. 2024 Apr 12;12(4):859. doi: 10.3390/biomedicines12040859. Biomedicines. 2024. PMID: 38672213 Free PMC article. Review.
2,924 results