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Items: 1 to 50 of 319

1.

Control of Astrocyte Quiescence and Activation in a Synthetic Brain Hydrogel.

Galarza S, Crosby AJ, Pak C, Peyton SR.

Adv Healthc Mater. 2020 Jan 15:e1901419. doi: 10.1002/adhm.201901419. [Epub ahead of print]

PMID:
31943839
2.

Variants in NIPAL4 and ALOXE3 cause autosomal recessive congenital ichthyosis in Pakistani families.

Akbar A, Bint-E-Farrakh M, Crosby AH, Gul A, Harlalka GV.

Congenit Anom (Kyoto). 2019 Dec 27. doi: 10.1111/cga.12366. [Epub ahead of print] No abstract available.

PMID:
31883158
3.

Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families.

Khan S, Rawlins LE, Harlalka GV, Umair M, Ullah A, Shahzad S, Javed M, Baple EL, Crosby AH, Ahmad W, Gul A.

BMC Med Genet. 2019 Dec 18;20(1):199. doi: 10.1186/s12881-019-0907-7.

4.

Lipid metabolic pathways converge in motor neuron degenerative diseases.

Rickman OJ, Baple EL, Crosby AH.

Brain. 2019 Dec 18. pii: awz382. doi: 10.1093/brain/awz382. [Epub ahead of print]

PMID:
31848577
5.

Port Strategies for Robot-Assisted Lobectomy by High-Volume Thoracic Surgeons: A Nationwide Survey.

Oh DS, Tisol WB, Cesnik L, Crosby A, Cerfolio RJ.

Innovations (Phila). 2019 Nov/Dec;14(6):545-552. doi: 10.1177/1556984519883643. Epub 2019 Nov 19.

PMID:
31739719
6.

The effect of size-scale on the kinematics of elastic energy release.

Ilton M, Cox SM, Egelmeers T, Sutton GP, Patek SN, Crosby AJ.

Soft Matter. 2019 Nov 27;15(46):9579-9586. doi: 10.1039/c9sm00870e.

PMID:
31724691
7.

Impact of Pre-bypass Autologous Blood Collection on Blood Transfusion Rates.

Crosby AD, Sistino JJ.

J Extra Corpor Technol. 2019 Sep;51(3):140-146.

PMID:
31548735
8.

MNS1 variant associated with situs inversus and male infertility.

Leslie JS, Rawlins LE, Chioza BA, Olubodun OR, Salter CG, Fasham J, Jones HF, Cross HE, Lam S, Harlalka GV, Muggenthaler MMA, Crosby AH, Baple EL.

Eur J Hum Genet. 2020 Jan;28(1):50-55. doi: 10.1038/s41431-019-0489-z. Epub 2019 Sep 18.

9.

A small gene sequencing panel realises a high diagnostic rate in patients with congenital nystagmus following basic phenotyping.

O'Gorman L, Norman CS, Michaels L, Newall T, Crosby AH, Mattocks C, Cree AJ, Lotery AJ, Baple EL, Ratnayaka JA, Baralle D, Lee H, Osborne D, Shawkat F, Gibson J, Ennis S, Self JE.

Sci Rep. 2019 Sep 13;9(1):13229. doi: 10.1038/s41598-019-49368-7.

10.

Residual strain effects in needle-induced cavitation.

Barney CW, Zheng Y, Wu S, Cai S, Crosby AJ.

Soft Matter. 2019 Sep 25;15(37):7390-7397. doi: 10.1039/c9sm01173k.

PMID:
31469148
11.

Novel nonsense variants in SLURP1 and DSG1 cause palmoplantar keratoderma in Pakistani families.

Akbar A, Prince C, Payne C, Fasham J, Ahmad W, Baple EL, Crosby AH, Harlalka GV, Gul A.

BMC Med Genet. 2019 Aug 23;20(1):145. doi: 10.1186/s12881-019-0872-1.

12.

Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches.

Shribman S, Reid E, Crosby AH, Houlden H, Warner TT.

Lancet Neurol. 2019 Dec;18(12):1136-1146. doi: 10.1016/S1474-4422(19)30235-2. Epub 2019 Jul 31. Review.

PMID:
31377012
13.

How typhoons trigger turbidity currents in submarine canyons.

Sequeiros OE, Bolla Pittaluga M, Frascati A, Pirmez C, Masson DG, Weaver P, Crosby AR, Lazzaro G, Botter G, Rimmer JG.

Sci Rep. 2019 Jun 25;9(1):9220. doi: 10.1038/s41598-019-45615-z.

14.

Macroscopic Geometry-Dominated Orientation of Symmetric Microwrinkle Patterns.

Hsueh HY, Chen MS, Liaw CY, Chen YC, Crosby AJ.

ACS Appl Mater Interfaces. 2019 Jul 3;11(26):23741-23749. doi: 10.1021/acsami.9b05264. Epub 2019 Jun 14.

PMID:
31199114
15.

Delineating the expanding phenotype associated with SCAPER gene mutation.

Fasham J, Arno G, Lin S, Xu M, Carss KJ, Hull S, Lane A, Robson AG, Wenger O, Self JE, Harlalka GV, Salter CG, Schema L, Moss TJ, Cheetham ME, Moore AT, Raymond FL, Chen R, Baple EL, Webster AR, Crosby AH; NIHR Bioresource Rare Diseases Consortium.

Am J Med Genet A. 2019 Aug;179(8):1665-1671. doi: 10.1002/ajmg.a.61202. Epub 2019 Jun 13. No abstract available.

16.

BBS5 and INPP5E mutations associated with ciliopathy disorders in families from Pakistan.

Khan S, Lin S, Harlalka GV, Ullah A, Shah K, Khalid S, Mehmood S, Hassan MJ, Ahmad W, Self JE, Crosby AH, Baple EL, Gul A.

Ann Hum Genet. 2019 Nov;83(6):477-482. doi: 10.1111/ahg.12336. Epub 2019 Jun 7.

PMID:
31173343
17.

Troyer Syndrome.

Baple E, Crosby A.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020.
2004 Nov 16 [updated 2019 Jun 6].

18.

Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic aging.

Jeffries AR, Maroofian R, Salter CG, Chioza BA, Cross HE, Patton MA, Dempster E, Temple IK, Mackay DJG, Rezwan FI, Aksglaede L, Baralle D, Dabir T, Hunter MF, Kamath A, Kumar A, Newbury-Ecob R, Selicorni A, Springer A, Van Maldergem L, Varghese V, Yachelevich N, Tatton-Brown K, Mill J, Crosby AH, Baple EL.

Genome Res. 2019 Jul;29(7):1057-1066. doi: 10.1101/gr.243584.118. Epub 2019 Jun 3.

19.

Intracellular iron deficiency in pulmonary arterial smooth muscle cells induces pulmonary arterial hypertension in mice.

Lakhal-Littleton S, Crosby A, Frise MC, Mohammad G, Carr CA, Loick PAM, Robbins PA.

Proc Natl Acad Sci U S A. 2019 Jun 25;116(26):13122-13130. doi: 10.1073/pnas.1822010116. Epub 2019 May 31.

20.

Effects of Digit Orientation on Gecko Adhesive Force Capacity: Synthetic and Behavioral Studies.

Imburgia MJ, Kuo CY, Briggs DR, Irschick DJ, Crosby AJ.

Integr Comp Biol. 2019 Jul 1;59(1):182-192. doi: 10.1093/icb/icz024.

PMID:
31004492
21.

Tyrosinase (TYR) gene sequencing and literature review reveals recurrent mutations and multiple population founder gene mutations as causative of oculocutaneous albinism (OCA) in Pakistani families.

Shakil M, Harlalka GV, Ali S, Lin S, D'Atri I, Hussain S, Nasir A, Shahzad MA, Ullah MI, Self JE, Baple EL, Crosby AH, Mahmood S.

Eye (Lond). 2019 Aug;33(8):1339-1346. doi: 10.1038/s41433-019-0436-9. Epub 2019 Apr 17.

PMID:
30996339
22.

Copy number variation of LINGO1 in familial dystonic tremor.

Alakbarzade V, Iype T, Chioza BA, Singh R, Harlalka GV, Hardy H, Sreekantan-Nair A, Proukakis C, Peall K, Clark LN, Caswell R, Lango Allen H, Wakeling M, Chilton JK, Baple EL, Louis ED, Warner TT, Crosby AH.

Neurol Genet. 2019 Feb 4;5(1):e307. doi: 10.1212/NXG.0000000000000307. eCollection 2019 Feb.

23.

A novel cyclic biased agonist of the apelin receptor, MM07, is disease modifying in the rat monocrotaline model of pulmonary arterial hypertension.

Yang P, Read C, Kuc RE, Nyimanu D, Williams TL, Crosby A, Buonincontri G, Southwood M, Sawiak SJ, Glen RC, Morrell NW, Davenport AP, Maguire JJ.

Br J Pharmacol. 2019 May;176(9):1206-1221. doi: 10.1111/bph.14603. Epub 2019 Apr 1.

24.

Suicide among veterinarians in the United States from 1979 through 2015.

Tomasi SE, Fechter-Leggett ED, Edwards NT, Reddish AD, Crosby AE, Nett RJ.

J Am Vet Med Assoc. 2019 Jan 1;254(1):104-112. doi: 10.2460/javma.254.1.104.

25.

Biomechanical properties of female dolphin reproductive tissue.

Orbach DN, Rattan S, Hogan M, Crosby AJ, Brennan PLR.

Acta Biomater. 2019 Mar 1;86:117-124. doi: 10.1016/j.actbio.2019.01.012. Epub 2019 Jan 11.

PMID:
30641290
26.

An Amish founder variant consolidates disruption of CEP55 as a cause of hydranencephaly and renal dysplasia.

Rawlins LE, Jones H, Wenger O, Aye M, Fasham J, Harlalka GV, Chioza BA, Miron A, Ellard S, Wakeling M, Crosby AH, Baple EL.

Eur J Hum Genet. 2019 Apr;27(4):657-662. doi: 10.1038/s41431-018-0306-0. Epub 2019 Jan 8.

27.

Self-Directed Violence After Medical Emergency Department Visits Among Youth.

Wang J, Xie H, Holland KM, Sumner SA, Balaji AB, David-Ferdon CF, Crosby AE.

Am J Prev Med. 2019 Feb;56(2):205-214. doi: 10.1016/j.amepre.2018.09.014. Epub 2018 Dec 17.

PMID:
30573334
28.

Growth/differentiation factor 15 causes TGFβ-activated kinase 1-dependent muscle atrophy in pulmonary arterial hypertension.

Garfield BE, Crosby A, Shao D, Yang P, Read C, Sawiak S, Moore S, Parfitt L, Harries C, Rice M, Paul R, Ormiston ML, Morrell NW, Polkey MI, Wort SJ, Kemp PR.

Thorax. 2019 Feb;74(2):164-176. doi: 10.1136/thoraxjnl-2017-211440. Epub 2018 Dec 15.

29.

Image-Based 3-Dimensional Characterization of Laryngotracheal Stenosis in Children.

McDaniel LS, Poynot WJ, Gonthier KA, Dunham ME, Crosby ATW.

OTO Open. 2018 Jan 29;2(1):2473974X17753583. doi: 10.1177/2473974X17753583. eCollection 2018 Jan-Mar.

30.

Application of Rubrene Air-Gap Transistors as Sensitive MEMS Physical Sensors.

Pereira MJ, Matta M, Hirsch L, Dufour I, Briseno A, Gali SM, Olivier Y, Muccioli L, Crosby A, Ayela C, Wantz G.

ACS Appl Mater Interfaces. 2018 Dec 5;10(48):41570-41577. doi: 10.1021/acsami.8b15319. Epub 2018 Nov 16.

PMID:
30398330
31.

RISING SUN: Prioritized Outcomes for Suicide Prevention in the Arctic.

Collins PY, Delgado RA Jr, Apok C, Baez L, Bjerregaard P, Chatwood S, Chipp C, Crawford A, Crosby A, Dillard D, Driscoll D, Ericksen H, Hicks J, Larsen CVL, McKeon R, Partapuoli PJ, Phillips A, Pringle B, Rasmus S, Sigurðardóttir S, Silviken A, Stoor JP, Sumarokov Y, Wexler L.

Psychiatr Serv. 2019 Feb 1;70(2):152-155. doi: 10.1176/appi.ps.201700505. Epub 2018 Oct 24.

PMID:
30353789
32.

Cross-platform mechanical characterization of lung tissue.

Polio SR, Kundu AN, Dougan CE, Birch NP, Aurian-Blajeni DE, Schiffman JD, Crosby AJ, Peyton SR.

PLoS One. 2018 Oct 17;13(10):e0204765. doi: 10.1371/journal.pone.0204765. eCollection 2018.

33.

Novel mutations in ALDH1A3 associated with autosomal recessive anophthalmia/microphthalmia, and review of the literature.

Lin S, Harlalka GV, Hameed A, Reham HM, Yasin M, Muhammad N, Khan S, Baple EL, Crosby AH, Saleha S.

BMC Med Genet. 2018 Sep 10;19(1):160. doi: 10.1186/s12881-018-0678-6.

34.

Efforts and Opportunities to Understand Women's Mortality Due to Suicide and Homicide Using the National Violent Death Reporting System.

Ivey-Stephenson AZ, Blair JM, Crosby AE.

J Womens Health (Larchmt). 2018 Sep;27(9):1073-1081. doi: 10.1089/jwh.2018.7320.

35.

Hematopoietic stem cell transplantation alters susceptibility to pulmonary hypertension in Bmpr2-deficient mice.

Crosby A, Toshner MR, Southwood MR, Soon E, Dunmore BJ, Groves E, Moore S, Wright P, Ottersbach K, Bennett C, Guerrero J, Ghevaert C, Morrell NW.

Pulm Circ. 2018 Oct-Dec;8(4):2045894018801642. doi: 10.1177/2045894018801642. Epub 2018 Aug 30.

36.

Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies.

Yuan B, Neira J, Pehlivan D, Santiago-Sim T, Song X, Rosenfeld J, Posey JE, Patel V, Jin W, Adam MP, Baple EL, Dean J, Fong CT, Hickey SE, Hudgins L, Leon E, Madan-Khetarpal S, Rawlins L, Rustad CF, Stray-Pedersen A, Tveten K, Wenger O, Diaz J, Jenkins L, Martin L, McGuire M, Pietryga M, Ramsdell L, Slattery L; DDD Study, Abid F, Bertuch AA, Grange D, Immken L, Schaaf CP, Van Esch H, Bi W, Cheung SW, Breman AM, Smith JL, Shaw C, Crosby AH, Eng C, Yang Y, Lupski JR, Xiao R, Liu P.

Genet Med. 2019 Mar;21(3):663-675. doi: 10.1038/s41436-018-0085-6. Epub 2018 Aug 30.

37.

Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa.

Li L, Jiao X, D'Atri I, Ono F, Nelson R, Chan CC, Nakaya N, Ma Z, Ma Y, Cai X, Zhang L, Lin S, Hameed A, Chioza BA, Hardy H, Arno G, Hull S, Khan MI, Fasham J, Harlalka GV, Michaelides M, Moore AT, Coban Akdemir ZH, Jhangiani S, Lupski JR, Cremers FPM, Qamar R, Salman A, Chilton J, Self J, Ayyagari R, Kabir F, Naeem MA, Ali M, Akram J, Sieving PA, Riazuddin S, Baple EL, Riazuddin SA, Crosby AH, Hejtmancik JF.

PLoS Genet. 2018 Aug 29;14(8):e1007504. doi: 10.1371/journal.pgen.1007504. eCollection 2018 Aug.

38.

Violence-Related Disparities Experienced by Black Youth and Young Adults: Opportunities for Prevention.

Sheats KJ, Irving SM, Mercy JA, Simon TR, Crosby AE, Ford DC, Merrick MT, Annor FB, Morgan RE.

Am J Prev Med. 2018 Oct;55(4):462-469. doi: 10.1016/j.amepre.2018.05.017. Epub 2018 Aug 20.

39.

Vital Signs: Trends in State Suicide Rates - United States, 1999-2016 and Circumstances Contributing to Suicide - 27 States, 2015.

Stone DM, Simon TR, Fowler KA, Kegler SR, Yuan K, Holland KM, Ivey-Stephenson AZ, Crosby AE.

MMWR Morb Mortal Wkly Rep. 2018 Jun 8;67(22):617-624. doi: 10.15585/mmwr.mm6722a1.

40.

Micromechanical characterization of soft, biopolymeric hydrogels: stiffness, resilience, and failure.

Rattan S, Li L, Lau HK, Crosby AJ, Kiick KL.

Soft Matter. 2018 May 9;14(18):3478-3489. doi: 10.1039/c8sm00501j.

PMID:
29700541
41.

The principles of cascading power limits in small, fast biological and engineered systems.

Ilton M, Bhamla MS, Ma X, Cox SM, Fitchett LL, Kim Y, Koh JS, Krishnamurthy D, Kuo CY, Temel FZ, Crosby AJ, Prakash M, Sutton GP, Wood RJ, Azizi E, Bergbreiter S, Patek SN.

Science. 2018 Apr 27;360(6387). pii: eaao1082. doi: 10.1126/science.aao1082.

PMID:
29700237
43.

Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies.

Salter CG, Beijer D, Hardy H, Barwick KES, Bower M, Mademan I, De Jonghe P, Deconinck T, Russell MA, McEntagart MM, Chioza BA, Blakely RD, Chilton JK, De Bleecker J, Baets J, Baple EL, Walk D, Crosby AH.

Neurol Genet. 2018 Mar 23;4(2):e222. doi: 10.1212/NXG.0000000000000222. eCollection 2018 Apr.

44.

miR-322-5p targets IGF-1 and is suppressed in the heart of rats with pulmonary hypertension.

Connolly M, Garfield BE, Crosby A, Morrell NW, Wort SJ, Kemp PR.

FEBS Open Bio. 2018 Jan 24;8(3):339-348. doi: 10.1002/2211-5463.12369. eCollection 2018 Mar.

45.

Identification of novel L2HGDH mutation in a large consanguineous Pakistani family- a case report.

Ullah MI, Nasir A, Ahmad A, Harlalka GV, Ahmad W, Hassan MJ, Baple EL, Crosby AH, Chioza BA.

BMC Med Genet. 2018 Feb 20;19(1):25. doi: 10.1186/s12881-018-0532-x.

46.

Mesoscale Block Copolymers.

Barber DM, Crosby AJ, Emrick T.

Adv Mater. 2018 Mar;30(13):e1706118. doi: 10.1002/adma.201706118. Epub 2018 Jan 30.

PMID:
29380431
47.

How Ligands Affect Resistive Switching in Solution-Processed HfO2 Nanoparticle Assemblies.

Wang J, Choudhary S, De Roo J, De Keukeleere K, Van Driessche I, Crosby AJ, Nonnenmann SS.

ACS Appl Mater Interfaces. 2018 Feb 7;10(5):4824-4830. doi: 10.1021/acsami.7b17376. Epub 2018 Jan 29.

PMID:
29338165
48.

Methods and Findings from the National Violent Death Reporting System for Identifying Gang-Like Homicides, 2005-2008.

Frazier L Jr, Ortega L, Patel N, Barnes J, Crosby AE, Hempstead K.

J Natl Med Assoc. 2017 Winter;109(4):272-278. doi: 10.1016/j.jnma.2017.03.001. Epub 2017 May 5.

49.

CommWalker: correctly evaluating modules in molecular networks in light of annotation bias.

Luecken MD, Page MJT, Crosby AJ, Mason S, Reinert G, Deane CM.

Bioinformatics. 2018 Mar 15;34(6):994-1000. doi: 10.1093/bioinformatics/btx706.

50.

Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization.

Wang H, Salter CG, Refai O, Hardy H, Barwick KES, Akpulat U, Kvarnung M, Chioza BA, Harlalka G, Taylan F, Sejersen T, Wright J, Zimmerman HH, Karakaya M, Stüve B, Weis J, Schara U, Russell MA, Abdul-Rahman OA, Chilton J, Blakely RD, Baple EL, Cirak S, Crosby AH.

Brain. 2017 Nov 1;140(11):2838-2850. doi: 10.1093/brain/awx249.

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