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Items: 18

1.

Activation of plasma membrane H+-ATPases participates in dormancy alleviation in sunflower seeds.

De Bont L, Naim E, Arbelet-Bonnin D, Xia Q, Palm E, Meimoun P, Mancuso S, El-Maarouf-Bouteau H, Bouteau F.

Plant Sci. 2019 Mar;280:408-415. doi: 10.1016/j.plantsci.2018.12.015. Epub 2018 Dec 18.

PMID:
30824019
2.

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability.

Kaya N, Alsagob M, D'Adamo MC, Al-Bakheet A, Hasan S, Muccioli M, Almutairi FB, Almass R, Aldosary M, Monies D, Mustafa OM, Alyounes B, Kenana R, Al-Zahrani J, Naim E, Binhumaid FS, Qari A, Almutairi F, Meyer B, Plageman TF, Pessia M, Colak D, Al-Owain M.

J Med Genet. 2016 Nov;53(11):786-792. doi: 10.1136/jmedgenet-2015-103637. Epub 2016 Aug 31.

PMID:
27582084
3.

Exome-based case-control association study using extreme phenotype design reveals novel candidates with protective effect in diabetic retinopathy.

Shtir C, Aldahmesh MA, Al-Dahmash S, Abboud E, Alkuraya H, Abouammoh MA, Nowailaty SR, Al-Thubaiti G, Naim EA, ALYounes B, Binhumaid FS, ALOtaibi AB, Altamimi AS, Alamer FH, Hashem M, Abouelhoda M, Monies D, Alkuraya FS.

Hum Genet. 2016 Feb;135(2):193-200. doi: 10.1007/s00439-015-1624-8. Epub 2015 Dec 22.

PMID:
26693933
4.

Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies.

Patel N, Aldahmesh MA, Alkuraya H, Anazi S, Alsharif H, Khan AO, Sunker A, Al-Mohsen S, Abboud EB, Nowilaty SR, Alowain M, Al-Zaidan H, Al-Saud B, Alasmari A, Abdel-Salam GM, Abouelhoda M, Abdulwahab FM, Ibrahim N, Naim E, Al-Younes B, E AlMostafa A, AlIssa A, Hashem M, Buzovetsky O, Xiong Y, Monies D, Altassan N, Shaheen R, Al-Hazzaa SA, Alkuraya FS.

Genet Med. 2016 Jun;18(6):554-62. doi: 10.1038/gim.2015.127. Epub 2015 Sep 10.

PMID:
26355662
5.

Expanding phenotypic and allelic heterogeneity of tricho-hepato-enteric syndrome.

Monies DM, Rahbeeni Z, Abouelhoda M, Naim EA, Al-Younes B, Meyer BF, Al-Mehaidib A.

J Pediatr Gastroenterol Nutr. 2015 Mar;60(3):352-6. doi: 10.1097/MPG.0000000000000627.

PMID:
25714577
6.

Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.

Alazami AM, Patel N, Shamseldin HE, Anazi S, Al-Dosari MS, Alzahrani F, Hijazi H, Alshammari M, Aldahmesh MA, Salih MA, Faqeih E, Alhashem A, Bashiri FA, Al-Owain M, Kentab AY, Sogaty S, Al Tala S, Temsah MH, Tulbah M, Aljelaify RF, Alshahwan SA, Seidahmed MZ, Alhadid AA, Aldhalaan H, AlQallaf F, Kurdi W, Alfadhel M, Babay Z, Alsogheer M, Kaya N, Al-Hassnan ZN, Abdel-Salam GM, Al-Sannaa N, Al Mutairi F, El Khashab HY, Bohlega S, Jia X, Nguyen HC, Hammami R, Adly N, Mohamed JY, Abdulwahab F, Ibrahim N, Naim EA, Al-Younes B, Meyer BF, Hashem M, Shaheen R, Xiong Y, Abouelhoda M, Aldeeri AA, Monies DM, Alkuraya FS.

Cell Rep. 2015 Jan 13;10(2):148-61. doi: 10.1016/j.celrep.2014.12.015. Epub 2014 Dec 31.

7.

Association of a mutation in LACC1 with a monogenic form of systemic juvenile idiopathic arthritis.

Wakil SM, Monies DM, Abouelhoda M, Al-Tassan N, Al-Dusery H, Naim EA, Al-Younes B, Shinwari J, Al-Mohanna FA, Meyer BF, Al-Mayouf S.

Arthritis Rheumatol. 2015 Jan;67(1):288-95. doi: 10.1002/art.38877.

8.

Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome.

Monies DM, Al-Hindi HN, Al-Muhaizea MA, Jaroudi DJ, Al-Younes B, Naim EA, Wakil SM, Meyer BF, Bohlega S.

Neuromuscul Disord. 2014 Apr;24(4):353-9. doi: 10.1016/j.nmd.2013.12.010. Epub 2014 Jan 4.

PMID:
24461433
9.

Systematic condition-dependent annotation of metabolic genes.

Shlomi T, Herrgard M, Portnoy V, Naim E, Palsson BØ, Sharan R, Ruppin E.

Genome Res. 2007 Nov;17(11):1626-33. Epub 2007 Sep 25.

10.

Adverse effects of antiretroviral drugs on HIV-1-infected and -uninfected human monocyte-derived macrophages.

Azzam R, Lal L, Goh SL, Kedzierska K, Jaworowski A, Naim E, Cherry CL, Wesselingh SL, Mills J, Crowe SM.

J Acquir Immune Defic Syndr. 2006 May;42(1):19-28.

PMID:
16639337
11.

Normal CD16 expression and phagocytosis of Mycobacterium avium complex by monocytes from a current cohort of HIV-1-infected patients.

Jaworowski A, Ellery P, Maslin CL, Naim E, Heinlein AC, Ryan CE, Paukovics G, Hocking J, Sonza S, Crowe SM.

J Infect Dis. 2006 Mar 1;193(5):693-7. Epub 2006 Jan 31.

PMID:
16453265
12.

Mutagenesis of the epithelial polarity gene, discs large 1, perturbs nephrogenesis in the developing mouse kidney.

Naim E, Bernstein A, Bertram JF, Caruana G.

Kidney Int. 2005 Sep;68(3):955-65. Erratum in: Kidney Int. 2005 Oct;68(4):1922.

13.

Signs of the quadrupole moments of the 8(+) isomers in 88,90Zr.

Bendahan J, Broude C, Dafni E, Goldring G, Hass M, Naim E, Rafailovich MH.

Phys Rev C Nucl Phys. 1986 Apr;33(4):1517-1519. No abstract available.

PMID:
9953305
14.

Electric quadrupole moment of the 211Rn (63/2)- isomer: Absence of core deformation at very high spins.

Dafni E, Hass M, Naim E, Rafailovich MH, Berger A, Grawe H, Mahnke H.

Phys Rev Lett. 1985 Sep 16;55(12):1269-1272. No abstract available.

PMID:
10031773
16.

Adenyl cyclase of rat parotid gland. Activation by fluoride and norepinephrine.

Schramm M, Naim E.

J Biol Chem. 1970 Jun;245(12):3225-31. No abstract available.

17.

The effect of calcium on amylase secretion by rat parotid slices.

Selinger Z, Naim E.

Biochim Biophys Acta. 1970 Apr 21;203(2):335-7. No abstract available.

PMID:
4315052
18.

ATP-dependent calcium uptake by microsomal preparations from rat parotid and submaxillary glands.

Selinger Z, Naim E, Lasser M.

Biochim Biophys Acta. 1970 Apr 21;203(2):326-34. No abstract available.

PMID:
4245535

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