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Items: 1 to 20 of 33

1.

Artificial stone dust-induced functional and inflammatory abnormalities in exposed workers monitored quantitatively by biometrics.

Ophir N, Shai AB, Alkalay Y, Israeli S, Korenstein R, Kramer MR, Fireman E.

ERJ Open Res. 2016 Mar 17;2(1). pii: 00086-2015.

2.

A mutation in TP63 causing a mild ectodermal dysplasia phenotype.

Goldsmith T, Eytan O, Magal L, Solomon M, Israeli S, Warshauer E, Grafi-Cohen M, Aberdam D, van Bokhoven H, Zhou H, Sarig O, Sprecher E, Nousbeck J.

J Invest Dermatol. 2014 Aug;134(8):2277-80. doi: 10.1038/jid.2014.159. No abstract available.

3.

Molecular analysis of a series of Israeli families with Comèl-Netherton syndrome.

Israeli S, Sarig O, Garty BZ, Indelman M, Bergman R, Sprecher E, Goldberg I.

Dermatology. 2014;228(2):183-8. doi: 10.1159/000357560.

PMID:
24577329
4.

Healthy eating and physical activity.

Israeli S, Aspler S, Morad M, Merrick J.

Int J Adolesc Med Health. 2014;26(3):305-7. doi: 10.1515/ijamh-2014-0005. No abstract available.

PMID:
24572976
5.

Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris.

Eytan O, Qiaoli L, Nousbeck J, van Steensel MA, Burger B, Hohl D, Taïeb A, Prey S, Bachmann D, Avitan-Hersh E, Jin Chung H, Shemer A, Trau H, Bergman R, Fuchs-Telem D, Warshauer E, Israeli S, Itin PH, Sarig O, Uitto J, Sprecher E.

Br J Dermatol. 2014 May;170(5):1196-8. doi: 10.1111/bjd.12799. No abstract available.

PMID:
24359224
6.

A novel splice-site mutation in the AAGAB gene segregates with hereditary punctate palmoplantar keratoderma and congenital dysplasia of the hip in a large family.

Eytan O, Sarig O, Israeli S, Mevorah B, Basel-Vanagaite L, Sprecher E.

Clin Exp Dermatol. 2014 Mar;39(2):182-6. doi: 10.1111/ced.12213.

PMID:
24289292
7.

Met-induced membrane blebbing leads to amoeboid cell motility and invasion.

Laser-Azogui A, Diamant-Levi T, Israeli S, Roytman Y, Tsarfaty I.

Oncogene. 2014 Apr 3;33(14):1788-98. doi: 10.1038/onc.2013.138.

PMID:
23665680
8.

Non-syndromic autosomal recessive congenital ichthyosis in the Israeli population.

Israeli S, Goldberg I, Fuchs-Telem D, Bergman R, Indelman M, Bitterman-Deutsch O, Harel A, Mashiach Y, Sarig O, Sprecher E.

Clin Exp Dermatol. 2013 Dec;38(8):911-6. doi: 10.1111/ced.12148.

PMID:
23621129
9.

Semidominant inheritance in epidermolytic ichthyosis.

Nousbeck J, Padalon-Brauch G, Fuchs-Telem D, Israeli S, Sarig O, Sheffer R, Sprecher E.

J Invest Dermatol. 2013 Nov;133(11):2626-8. doi: 10.1038/jid.2013.193. No abstract available.

10.

The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12.

Goldsmith T, Fuchs-Telem D, Israeli S, Sarig O, Padalon-Brauch G, Bergman R, Indelman M, Sprecher E, Nousbeck J.

Exp Dermatol. 2013 Apr;22(4):251-4. doi: 10.1111/exd.12110.

PMID:
23528209
11.

Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation.

Sarig O, Nahum S, Rapaport D, Ishida-Yamamoto A, Fuchs-Telem D, Qiaoli L, Cohen-Katsenelson K, Spiegel R, Nousbeck J, Israeli S, Borochowitz ZU, Padalon-Brauch G, Uitto J, Horowitz M, Shalev S, Sprecher E.

Am J Hum Genet. 2012 Aug 10;91(2):337-42. doi: 10.1016/j.ajhg.2012.06.003.

12.

Familial pityriasis rubra pilaris is caused by mutations in CARD14.

Fuchs-Telem D, Sarig O, van Steensel MA, Isakov O, Israeli S, Nousbeck J, Richard K, Winnepenninckx V, Vernooij M, Shomron N, Uitto J, Fleckman P, Richard G, Sprecher E.

Am J Hum Genet. 2012 Jul 13;91(1):163-70. doi: 10.1016/j.ajhg.2012.05.010.

13.

Basal insulin and cardiovascular and other outcomes in dysglycemia.

ORIGIN Trial Investigators., Gerstein HC, Bosch J, Dagenais GR, Díaz R, Jung H, Maggioni AP, Pogue J, Probstfield J, Ramachandran A, Riddle MC, Rydén LE, Yusuf S.

N Engl J Med. 2012 Jul 26;367(4):319-28. doi: 10.1056/NEJMoa1203858.

14.

n-3 fatty acids and cardiovascular outcomes in patients with dysglycemia.

ORIGIN Trial Investigators., Bosch J, Gerstein HC, Dagenais GR, Díaz R, Dyal L, Jung H, Maggiono AP, Probstfield J, Ramachandran A, Riddle MC, Rydén LE, Yusuf S.

N Engl J Med. 2012 Jul 26;367(4):309-18. doi: 10.1056/NEJMoa1203859.

15.

Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris.

Sarig O, Bercovici S, Zoller L, Goldberg I, Indelman M, Nahum S, Israeli S, Sagiv N, Martinez de Morentin H, Katz O, Baum S, Barzilai A, Trau H, Murrell DF, Bergman R, Hertl M, Rosenberg S, Nöthen MM, Skorecki K, Schmidt E, Zillikens D, Darvasi A, Geiger D, Rosset S, Ibrahim SM, Sprecher E.

J Invest Dermatol. 2012 Jul;132(7):1798-805. doi: 10.1038/jid.2012.46.

16.

β1 integrin gene excision in the adult murine cardiac myocyte causes defective mechanical and signaling responses.

Li R, Wu Y, Manso AM, Gu Y, Liao P, Israeli S, Yajima T, Nguyen U, Huang MS, Dalton ND, Peterson KL, Ross RS.

Am J Pathol. 2012 Mar;180(3):952-62. doi: 10.1016/j.ajpath.2011.12.007.

17.

Inflammatory peeling skin syndrome caused a novel mutation in CDSN.

Telem DF, Israeli S, Sarig O, Sprecher E.

Arch Dermatol Res. 2012 Apr;304(3):251-5. doi: 10.1007/s00403-011-1195-z.

PMID:
22146835
18.

Epigenetic silencing of the tumor suppressor klotho in human breast cancer.

Rubinek T, Shulman M, Israeli S, Bose S, Avraham A, Zundelevich A, Evron E, Gal-Yam EN, Kaufman B, Wolf I.

Breast Cancer Res Treat. 2012 Jun;133(2):649-57. doi: 10.1007/s10549-011-1824-4.

PMID:
22042362
19.

Beneficial effect of acitretin in Chanarin-Dorfman syndrome.

Israeli S, Pessach Y, Sarig O, Goldberg I, Sprecher E.

Clin Exp Dermatol. 2012 Jan;37(1):31-3. doi: 10.1111/j.1365-2230.2011.04164.x.

PMID:
21981352
20.

The peptide-hormone glucagon-like peptide-1 activates cAMP and inhibits growth of breast cancer cells.

Ligumsky H, Wolf I, Israeli S, Haimsohn M, Ferber S, Karasik A, Kaufman B, Rubinek T.

Breast Cancer Res Treat. 2012 Apr;132(2):449-61. doi: 10.1007/s10549-011-1585-0.

PMID:
21638053
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