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Items: 1 to 20 of 416

1.

Reply to Graham et al.: In silico atomistic coordinates and molecular dynamics simulation trajectories of the glucocerebrosidase-saposin C complex.

Romero R, Yuen T, New MI, Zaidi M, Haider S.

Proc Natl Acad Sci U S A. 2019 Jun 4;116(23):11101-11102. doi: 10.1073/pnas.1905744116. No abstract available.

PMID:
31164477
2.

Mechanism of glucocerebrosidase activation and dysfunction in Gaucher disease unraveled by molecular dynamics and deep learning.

Romero R, Ramanathan A, Yuen T, Bhowmik D, Mathew M, Munshi LB, Javaid S, Bloch M, Lizneva D, Rahimova A, Khan A, Taneja C, Kim SM, Sun L, New MI, Haider S, Zaidi M.

Proc Natl Acad Sci U S A. 2019 Mar 12;116(11):5086-5095. doi: 10.1073/pnas.1818411116. Epub 2019 Feb 26.

3.

Introduction: Contemporary perspectives on congenital adrenal hyperplasia: impacts on reproduction.

New MI, Rosenwaks Z.

Fertil Steril. 2019 Jan;111(1):4-6. doi: 10.1016/j.fertnstert.2018.11.031.

PMID:
30611412
4.

Fertility in patients with nonclassical congenital adrenal hyperplasia.

New MI, Ghizzoni L, Meyer-Bahlburg H, Khattab A, Reichman D, Rosenwaks Z.

Fertil Steril. 2019 Jan;111(1):13-20. doi: 10.1016/j.fertnstert.2018.11.023. Review.

PMID:
30611403
5.

FSIP1 regulates autophagy in breast cancer.

Liu C, Sun L, Yang J, Liu T, Yang Y, Kim SM, Ou X, Wang Y, Sun L, Zaidi M, New MI, Yuen T, Guo Q.

Proc Natl Acad Sci U S A. 2018 Dec 18;115(51):13075-13080. doi: 10.1073/pnas.1809681115. Epub 2018 Dec 3.

6.

A novel de novo frameshift mutation in NR0B1 and low prenatal estriol in adrenal hypoplasia congenita.

Khattab A, Nelson-Williams C, Cabreza V, Macdonald A, Loring E, Saland J, New MI.

Ann N Y Acad Sci. 2018 Dec;1433(1):7-11. doi: 10.1111/nyas.13962. Epub 2018 Aug 21.

PMID:
30129976
7.

FSH, Bone Mass, Body Fat, and Biological Aging.

Zaidi M, Lizneva D, Kim SM, Sun L, Iqbal J, New MI, Rosen CJ, Yuen T.

Endocrinology. 2018 Oct 1;159(10):3503-3514. doi: 10.1210/en.2018-00601.

8.

Human hydroxymethylbilane synthase: Molecular dynamics of the pyrrole chain elongation identifies step-specific residues that cause AIP.

Bung N, Roy A, Chen B, Das D, Pradhan M, Yasuda M, New MI, Desnick RJ, Bulusu G.

Proc Natl Acad Sci U S A. 2018 Apr 24;115(17):E4071-E4080. doi: 10.1073/pnas.1719267115. Epub 2018 Apr 9.

9.

Actions of pituitary hormones beyond traditional targets.

Zaidi M, New MI, Blair HC, Zallone A, Baliram R, Davies TF, Cardozo C, Iqbal J, Sun L, Rosen CJ, Yuen T.

J Endocrinol. 2018 Jun;237(3):R83-R98. doi: 10.1530/JOE-17-0680. Epub 2018 Mar 19. Review.

10.

Epitope-specific monoclonal antibodies to FSHβ increase bone mass.

Ji Y, Liu P, Yuen T, Haider S, He J, Romero R, Chen H, Bloch M, Kim SM, Lizneva D, Munshi L, Zhou C, Lu P, Iqbal J, Cheng Z, New MI, Hsueh AJ, Bian Z, Rosen CJ, Sun L, Zaidi M.

Proc Natl Acad Sci U S A. 2018 Feb 27;115(9):2192-2197. doi: 10.1073/pnas.1718144115. Epub 2018 Feb 12.

11.

Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.

Yau M, Haider S, Khattab A, Ling C, Mathew M, Zaidi S, Bloch M, Patel M, Ewert S, Abdullah W, Toygar A, Mudryi V, Al Badi M, Alzubdi M, Wilson RC, Al Azkawi HS, Ozdemir HN, Abu-Amer W, Hertecant J, Razzaghy-Azar M, Funder JW, Al Senani A, Sun L, Kim SM, Yuen T, Zaidi M, New MI.

Proc Natl Acad Sci U S A. 2017 Dec 26;114(52):E11248-E11256. doi: 10.1073/pnas.1716621115. Epub 2017 Dec 11.

12.

FSIP1 binds HER2 directly to regulate breast cancer growth and invasiveness.

Liu T, Zhang H, Sun L, Zhao D, Liu P, Yan M, Zaidi N, Izadmehr S, Gupta A, Abu-Amer W, Luo M, Yang J, Ou X, Wang Y, Bai X, Wang Y, New MI, Zaidi M, Yuen T, Liu C.

Proc Natl Acad Sci U S A. 2017 Jul 18;114(29):7683-7688. doi: 10.1073/pnas.1621486114. Epub 2017 Jul 3.

13.

Linking the degree of virilization in females with congenital adrenal hyperplasia to genotype.

Gurgov S, Bernabé KJ, Stites J, Cunniff CM, Lin-Su K, Felsen D, New MI, Poppas DP.

Ann N Y Acad Sci. 2017 Aug;1402(1):56-63. doi: 10.1111/nyas.13370. Epub 2017 Jun 22.

PMID:
28640966
14.

Blocking FSH induces thermogenic adipose tissue and reduces body fat.

Liu P, Ji Y, Yuen T, Rendina-Ruedy E, DeMambro VE, Dhawan S, Abu-Amer W, Izadmehr S, Zhou B, Shin AC, Latif R, Thangeswaran P, Gupta A, Li J, Shnayder V, Robinson ST, Yu YE, Zhang X, Yang F, Lu P, Zhou Y, Zhu LL, Oberlin DJ, Davies TF, Reagan MR, Brown A, Kumar TR, Epstein S, Iqbal J, Avadhani NG, New MI, Molina H, van Klinken JB, Guo EX, Buettner C, Haider S, Bian Z, Sun L, Rosen CJ, Zaidi M.

Nature. 2017 Jun 1;546(7656):107-112. doi: 10.1038/nature22342. Epub 2017 May 24.

15.

Stigma Associated with Classical Congenital Adrenal Hyperplasia in Women's Sexual Lives.

Meyer-Bahlburg HFL, Khuri J, Reyes-Portillo J, Ehrhardt AA, New MI.

Arch Sex Behav. 2018 May;47(4):943-951. doi: 10.1007/s10508-017-1003-8. Epub 2017 May 18.

PMID:
28523454
16.

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Khattab A, Haider S, Kumar A, Dhawan S, Alam D, Romero R, Burns J, Li D, Estatico J, Rahi S, Fatima S, Alzahrani A, Hafez M, Musa N, Razzghy Azar M, Khaloul N, Gribaa M, Saad A, Charfeddine IB, Bilharinho de Mendonça B, Belgorosky A, Dumic K, Dumic M, Aisenberg J, Kandemir N, Alikasifoglu A, Ozon A, Gonc N, Cheng T, Kuhnle-Krahl U, Cappa M, Holterhus PM, Nour MA, Pacaud D, Holtzman A, Li S, Zaidi M, Yuen T, New MI.

Proc Natl Acad Sci U S A. 2017 Mar 7;114(10):E1933-E1940. doi: 10.1073/pnas.1621082114. Epub 2017 Feb 22.

17.

Universal Haplotype-Based Noninvasive Prenatal Testing for Single Gene Diseases.

Hui WW, Jiang P, Tong YK, Lee WS, Cheng YK, New MI, Kadir RA, Chan KC, Leung TY, Lo YM, Chiu RW.

Clin Chem. 2017 Feb;63(2):513-524. doi: 10.1373/clinchem.2016.268375. Epub 2016 Dec 8.

18.

Syndrome-Related Stigma in the General Social Environment as Reported by Women with Classical Congenital Adrenal Hyperplasia.

Meyer-Bahlburg HF, Reyes-Portillo JA, Khuri J, Ehrhardt AA, New MI.

Arch Sex Behav. 2017 Feb;46(2):341-351. doi: 10.1007/s10508-016-0862-8. Epub 2016 Sep 27.

PMID:
27677267
19.

A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred.

Yau M, Azkawi HS, Haider S, Khattab A, Badi MA, Abdullah W, Senani AA, Wilson RC, Yuen T, Zaidi M, New MI.

Ann N Y Acad Sci. 2016 Jul;1376(1):65-71. doi: 10.1111/nyas.13162. Epub 2016 Aug 15.

PMID:
27526338
20.

Steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.

Parsa AA, New MI.

J Steroid Biochem Mol Biol. 2017 Jan;165(Pt A):2-11. doi: 10.1016/j.jsbmb.2016.06.015. Epub 2016 Jul 2. Review.

PMID:
27380651

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