Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 1 |
2006 | 1 |
2012 | 1 |
2013 | 1 |
2020 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Quoted phrase not found in phrase index: "Acromesomelic dysplasia 1, Maroteaux type"
Page 1
A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type.
Hum Mol Genet. 2013 Jan 15;22(2):345-57. doi: 10.1093/hmg/dds432. Epub 2012 Oct 12.
Hum Mol Genet. 2013.
PMID: 23065701
Free PMC article.
The Npr2(pwe/pwe) mouse is a model for the human skeletal dysplasia acromesomelic dysplasia, Maroteaux type (AMDM). We conducted a thorough analysis of the female reproductive tract and report that the primary cause of Npr2(pwe/pwe) female infertility …
The Npr2(pwe/pwe) mouse is a model for the human skeletal dysplasia acromesomelic dysplasia, Maroteaux type (AMD …
Acromesomelic Dysplasia, Type Maroteaux: Impact of Long-Term (8 Years) High-Dose Growth Hormone Treatment on Growth Velocity and Final Height in 2 Siblings.
Arya VB, Raj M, Younes M, Chapman S, Irving M, Kapoor RR, Buchanan CR.
Arya VB, et al.
Horm Res Paediatr. 2020;93(5):335-342. doi: 10.1159/000511874. Epub 2020 Nov 25.
Horm Res Paediatr. 2020.
PMID: 33238275
INTRODUCTION: Acromesomelic dysplasia, type Maroteaux (AMDM) is a rare autosomal recessive skeletal dysplasia, characterized by severe dwarfism and disproportionate limb shortening. ...GH provocation testing showed relatively high GH levels. Serum insu …
INTRODUCTION: Acromesomelic dysplasia, type Maroteaux (AMDM) is a rare autosomal recessive skeletal dysplasia, c …
Item in Clipboard
Natriuretic peptides, their receptors, and cyclic guanosine monophosphate-dependent signaling functions.
Potter LR, Abbey-Hosch S, Dickey DM.
Potter LR, et al.
Endocr Rev. 2006 Feb;27(1):47-72. doi: 10.1210/er.2005-0014. Epub 2005 Nov 16.
Endocr Rev. 2006.
PMID: 16291870
Review.
Natriuretic peptides are a family of structurally related but genetically distinct hormones/paracrine factors that regulate blood volume, blood pressure, ventricular hypertrophy, pulmonary hypertension, fat metabolism, and long bone growth. The mammalian members are atrial natriu …
Natriuretic peptides are a family of structurally related but genetically distinct hormones/paracrine factors that regulate blood volume, bl …
Item in Clipboard
Cite
Cite