Elhaji Y[au] - Search Results

Year	Number of Results
1999	1
2000	1
2001	2
2002	1
2003	1
2004	2
2006	1
2019	2
2020	1
2021	1
2023	1
2024	0

1

Nuclear receptors and disease: androgen receptor.

Gottlieb B, Beitel LK, Wu J, Elhaji YA, Trifiro M. Gottlieb B, et al. Among authors: elhaji ya. Essays Biochem. 2004;40:121-36. doi: 10.1042/bse0400121. Essays Biochem. 2004. PMID: 15242343 Review.

2

Establishment of persistent enteric mycobacterial infection following streptomycin pre-treatment.

Duffy SC, Lupien A, Elhaji Y, Farag M, Marcus V, Behr MA. Duffy SC, et al. Among authors: elhaji y. Gut Pathog. 2023 Oct 3;15(1):46. doi: 10.1186/s13099-023-00573-w. Gut Pathog. 2023. PMID: 37789445 Free PMC article.

3

Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family.

Elhaji Y, van Henten TMA, Ruivenkamp CAL, Nightingale M, Santen GW, Vos LE, Hull PR. Elhaji Y, et al. JID Innov. 2021 May 6;1(3):100022. doi: 10.1016/j.xjidi.2021.100022. eCollection 2021 Sep. JID Innov. 2021. PMID: 34909722 Free PMC article.

4

Filaggrin gene loss-of-function mutations constitute a factor in patients with multiple contact allergies.

Elhaji Y, Sasseville D, Pratt M, Asai Y, Matheson K, McLean WHI, Hull PR. Elhaji Y, et al. Contact Dermatitis. 2019 Jun;80(6):354-358. doi: 10.1111/cod.13268. Epub 2019 Apr 10. Contact Dermatitis. 2019. PMID: 30868611

5

AAGAB Mutations in 18 Canadian Families With Punctate Palmoplantar Keratoderma and a Possible Link to Cancer.

Elhaji Y, Hedlin C, Nath A, Price EL, Gallant C, Northgrave S, Hull PR. Elhaji Y, et al. J Cutan Med Surg. 2020 Jan/Feb;24(1):28-32. doi: 10.1177/1203475419878161. Epub 2019 Sep 16. J Cutan Med Surg. 2020. PMID: 31526046

6

A highly accurate, low cost test for BRCA1 mutations.

van Orsouw NJ, Dhanda RK, Elhaji Y, Narod SA, Li FP, Eng C, Vijg J. van Orsouw NJ, et al. Among authors: elhaji y. J Med Genet. 1999 Oct;36(10):747-53. doi: 10.1136/jmg.36.10.747. J Med Genet. 1999. PMID: 10528853 Free PMC article.

7

Cloning and characterization of an androgen receptor N-terminal-interacting protein with ubiquitin-protein ligase activity.

Beitel LK, Elhaji YA, Lumbroso R, Wing SS, Panet-Raymond V, Gottlieb B, Pinsky L, Trifiro MA. Beitel LK, et al. Among authors: elhaji ya. J Mol Endocrinol. 2002 Aug;29(1):41-60. doi: 10.1677/jme.0.0290041. J Mol Endocrinol. 2002. PMID: 12200228

8

An examination of how different mutations at arginine 855 of the androgen receptor result in different androgen insensitivity phenotypes.

Elhaji YA, Wu JH, Gottlieb B, Beitel LK, Alvarado C, Batist G, Trifiro MA. Elhaji YA, et al. Mol Endocrinol. 2004 Aug;18(8):1876-86. doi: 10.1210/me.2004-0023. Epub 2004 Apr 29. Mol Endocrinol. 2004. PMID: 15118070

9

Impaired helix 12 dynamics due to proline 892 substitutions in the androgen receptor are associated with complete androgen insensitivity.

Elhaji YA, Stoica I, Dennis S, Purisima EO, Lumbroso R, Beitel LK, Trifiro MA. Elhaji YA, et al. Hum Mol Genet. 2006 Mar 15;15(6):921-31. doi: 10.1093/hmg/ddl009. Epub 2006 Jan 31. Hum Mol Genet. 2006. PMID: 16449235

10

The use of androgen receptor amino/carboxyl-terminal interaction assays to investigate androgen receptor gene mutations in subjects with varying degrees of androgen insensitivity.

Ghali SA, Gottlieb B, Lumbroso R, Beitel LK, Elhaji Y, Wu J, Pinsky L, Trifiro MA. Ghali SA, et al. Among authors: elhaji y. J Clin Endocrinol Metab. 2003 May;88(5):2185-93. doi: 10.1210/jc.2002-021324. J Clin Endocrinol Metab. 2003. PMID: 12727974

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