A M Moses
Overview
Explore the profile of A M Moses including associated specialties, affiliations and a list of published articles.
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Articles
107
Citations
762
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Recent Articles
1.
Dhaliwal R, Cibula D, Ghosh C, Weinstock R, Moses A
Osteoporos Int
. 2014 Apr;
25(7):1969-73.
PMID: 24718377
Unlabelled: The increased risk for fractures in type 2 diabetes mellitus (T2DM) despite higher average bone density is unexplained. This study assessed trabecular bone quality in T2DM using the trabecular...
2.
Seton M, Moses A, Bode R, Schwartz C
Bone
. 2010 Sep;
48(2):281-5.
PMID: 20858558
Context: Paget's disease of bone (PDB) is a focal disorder of bone metabolism with overgrowth of affected bone resulting in the skeletal complications of this disease. Objective: This study examines...
3.
Moses A, Chiang D, Eisen M
Pac Symp Biocomput
. 2004 Mar;
:324-35.
PMID: 14992514
The preferential conservation of transcription factor binding sites implies that non-coding sequence data from related species will prove a powerful asset to motif discovery. We present a unified probabilistic framework...
4.
Moses A, Weinstock R
J Clin Endocrinol Metab
. 2001 Feb;
86(2):471-2.
PMID: 11157991
No abstract available.
5.
Buckler H, Fraser W, Hosking D, Ryan W, Maricic M, Singer F, et al.
Bone
. 1999 May;
24(5 Suppl):81S-85S.
PMID: 10321935
No abstract available.
6.
Namnoum A, Merriam G, Moses A, Levine M
J Clin Endocrinol Metab
. 1998 Mar;
83(3):824-9.
PMID: 9506735
Most individuals with Albright's hereditary osteodystrophy (AHO) have deficient expression or function of G(s alpha), the alpha subunit of the guanine nucleotide binding protein that stimulates adenylyl cyclase, and are...
7.
CANFIELD M, Tamarappoo B, Moses A, Verkman A, Holtzman E
Hum Mol Genet
. 1997 Sep;
6(11):1865-71.
PMID: 9302264
Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2). We studied a family which included a female patient with...
8.
Moses A, Sangani G, Miller J
J Clin Endocrinol Metab
. 1995 Apr;
80(4):1184-6.
PMID: 7714087
Almost all cases of congenital nephrogenic diabetes insipidus (NDI) are transmitted in an X-linked recessive manner by an asymptomatic carrier female to her affected son. Severe symptomatic NDI has not...
9.
Reinhart S, Norden A, Lapsley M, Thakker R, Pang J, Moses A, et al.
J Am Soc Nephrol
. 1995 Jan;
5(7):1451-61.
PMID: 7703383
X-linked recessive nephrolithiasis (XRN) was described in a large kindred in which nephrolithiasis; proximal tubular dysfunction, proteinuria, nephrocalcinosis, and renal failure occur only in males. Carrier females are asymptomatic, but...
10.