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Page 1
The DNA sequence and comparative analysis of human chromosome 10.
Deloukas P, Earthrowl ME, Grafham DV, Rubenfield M, French L, Steward CA, Sims SK, Jones MC, Searle S, Scott C, Howe K, Hunt SE, Andrews TD, Gilbert JG, Swarbreck D, Ashurst JL, Taylor A, Battles J, Bird CP, Ainscough R, Almeida JP, Ashwell RI, Ambrose KD, Babbage AK, Bagguley CL, Bailey J, Banerjee R, Bates K, Beasley H, Bray-Allen S, Brown AJ, Brown JY, Burford DC, Burrill W, Burton J, Cahill P, Camire D, Carter NP, Chapman JC, Clark SY, Clarke G, Clee CM, Clegg S, Corby N, Coulson A, Dhami P, Dutta I, Dunn M, Faulkner L, Frankish A, Frankland JA, Garner P, Garnett J, Gribble S, Griffiths C, Grocock R, Gustafson E, Hammond S, Harley JL, Hart E, Heath PD, Ho TP, Hopkins B, Horne J, Howden PJ, Huckle E, Hynds C, Johnson C, Johnson D, Kana A, Kay M, Kimberley AM, Kershaw JK, Kokkinaki M, Laird GK, Lawlor S, Lee HM, Leongamornlert DA, Laird G, Lloyd C, Lloyd DM, Loveland J, Lovell J, McLaren S, McLay KE, McMurray A, Mashreghi-Mohammadi M, Matthews L, Milne S, Nickerson T, Nguyen M, Overton-Larty E, Palmer SA, Pearce AV, Peck AI, Pelan S, Phillimore B, Porter K, Rice CM, Rogosin A, Ross MT, Sarafidou T, Sehra HK, Shownkeen R, Skuce CD, Smith M, Standring L, Sycamore N, Tester J, Thor… See abstract for full author list ➔ Deloukas P, et al. Among authors: walsh j. Nature. 2004 May 27;429(6990):375-81. doi: 10.1038/nature02462. Nature. 2004. PMID: 15164054
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD, et al. Weil D, et al. Among authors: walsh j. Nature. 1995 Mar 2;374(6517):60-1. doi: 10.1038/374060a0. Nature. 1995. PMID: 7870171
A type VII myosin encoded by the mouse deafness gene shaker-1.
Gibson F, Walsh J, Mburu P, Varela A, Brown KA, Antonio M, Beisel KW, Steel KP, Brown SD. Gibson F, et al. Among authors: walsh j. Nature. 1995 Mar 2;374(6517):62-4. doi: 10.1038/374062a0. Nature. 1995. PMID: 7870172
Unravelling the genetics of deafness.
Steel KP, Mburu P, Gibson F, Walsh J, Varela A, Brown K, Self T, Mahony M, Fleming J, Pearce A, Harvey D, Cable J, Brown SD. Steel KP, et al. Among authors: walsh j. Ann Otol Rhinol Laryngol Suppl. 1997 May;168:59-62. Ann Otol Rhinol Laryngol Suppl. 1997. PMID: 9153119 Review.
Mutation analysis of the mouse myosin VIIA deafness gene.
Mburu P, Liu XZ, Walsh J, Saw D Jr, Cope MJ, Gibson F, Kendrick-Jones J, Steel KP, Brown SD. Mburu P, et al. Among authors: walsh j. Genes Funct. 1997 Jun;1(3):191-203. doi: 10.1046/j.1365-4624.1997.00020.x. Genes Funct. 1997. PMID: 9680294
Sensorineural hearing impairment non-syndromic, dominant DFNA11.
Tamagawa Y, Kitamura K, Ishida T, Nishizawa M, Liu XZ, Walsh J, Steel KP, Brown SD. Tamagawa Y, et al. Among authors: walsh j. Adv Otorhinolaryngol. 2000;56:103-6. doi: 10.1159/000059092. Adv Otorhinolaryngol. 2000. PMID: 10868221 No abstract available.
Perspectives of People with Stroke, Caregivers and Healthcare Professionals on an Adaptive mHealth Intervention for Physical Activity in the Prevention of Secondary Stroke: A Qualitative Study.
Cardy N, Hunter A, Carter D, O'Donoghue M, Carvalho M, Carr E, Walsh JC, Bernhardt J, Fitzsimons C, Richardson I, Salsberg J, Glynn L, Walsh C, O'Driscoll E, Boland P, Cunningham N, Forbes J, Galvin R, Hayes S. Cardy N, et al. Among authors: walsh jc. J Multidiscip Healthc. 2024 May 30;17:2677-2688. doi: 10.2147/JMDH.S420530. eCollection 2024. J Multidiscip Healthc. 2024. PMID: 38831803 Free PMC article.
Vitamin D for the Prevention of Disease: An Endocrine Society Clinical Practice Guideline.
Demay MB, Pittas AG, Bikle DD, Diab DL, Kiely ME, Lazaretti-Castro M, Lips P, Mitchell DM, Murad MH, Powers S, Rao SD, Scragg R, Tayek JA, Valent AM, Walsh JME, McCartney CR. Demay MB, et al. Among authors: walsh jme. J Clin Endocrinol Metab. 2024 Jun 3:dgae290. doi: 10.1210/clinem/dgae290. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 38828931
5,882 results