Articles with public access mandates - Joan T RichtsmeierLearn more
Not available anywhere: 1
Mouse Models to Test Hypotheses of Human Evolution
N Martínez-Abadías, R Gonzàlez, R Mateu, J Sastre, A Robert-Moreno, ...
Evolutionary Cell Processes in Primates, 203-226, 2021
Mandates: US National Institutes of Health, Government of Spain
Available somewhere: 77
Angiogenesis and intramembranous osteogenesis
CJ Percival, JT Richtsmeier
Developmental Dynamics 242 (8), 909-922, 2013
Mandates: US National Institutes of Health
Hand in glove: brain and skull in development and dysmorphogenesis
JT Richtsmeier, K Flaherty
Acta neuropathologica 125, 469-489, 2013
Mandates: US National Institutes of Health
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
CM Justice, G Yagnik, Y Kim, I Peter, EW Jabs, M Erazo, X Ye, ...
Nature genetics 44 (12), 1360-1364, 2012
Mandates: US National Institutes of Health
Understanding craniosynostosis as a growth disorder
K Flaherty, N Singh, JT Richtsmeier
Wiley Interdisciplinary Reviews: Developmental Biology 5 (4), 429-459, 2016
Mandates: US National Science Foundation, US National Institutes of Health
Closing the gap: genetic and genomic continuum from syndromic to nonsyndromic craniosynostoses
Y Heuzé, G Holmes, I Peter, JT Richtsmeier, EW Jabs
Current genetic medicine reports 2, 135-145, 2014
Mandates: US National Institutes of Health
Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+P253R mice
Y Wang, M Sun, VL Uhlhorn, X Zhou, I Peter, N Martinez-Abadias, CA Hill, ...
BMC developmental biology 10, 1-20, 2010
Mandates: US National Institutes of Health
A non-mosaic transchromosomic mouse model of down syndrome carrying the long arm of human chromosome 21
Y Kazuki, FJ Gao, Y Li, AJ Moyer, B Devenney, K Hiramatsu, ...
Elife 9, e56223, 2020
Mandates: US National Institutes of Health
FGF/FGFR signaling coordinates skull development by modulating magnitude of morphological integration: evidence from Apert syndrome mouse models
N Martínez-Abadías, Y Heuzé, Y Wang, EW Jabs, K Aldridge, ...
PLoS One 6 (10), e26425, 2011
Mandates: US National Institutes of Health
New insights into the relationship between suture closure and craniofacial dysmorphology in sagittal nonsyndromic craniosynostosis
Y Heuzé, SA Boyadjiev, JL Marsh, AA Kane, E Cherkez, JE Boggan, ...
Journal of anatomy 217 (2), 85-96, 2010
Mandates: US National Institutes of Health
Beyond the closed suture in apert syndrome mouse models: evidence of primary effects of FGFR2 signaling on facial shape at birth
N Martínez‐Abadías, C Percival, K Aldridge, CA Hill, T Ryan, ...
Developmental Dynamics 239 (11), 3058-3071, 2010
Mandates: US National Institutes of Health
Morphological integration of the skull in craniofacial anomalies
JT Richtsmeier, VB DeLeon
Orthodontics & craniofacial research 12 (3), 149-158, 2009
Mandates: US National Institutes of Health
Unilateral and bilateral expression of a quantitative trait: asymmetry and symmetry in coronal craniosynostosis
Y Heuzé, N Martínez‐Abadías, JM Stella, CW Senders, SA Boyadjiev, ...
Journal of Experimental Zoology Part B: Molecular and Developmental …, 2012
Mandates: US National Institutes of Health
Phosphotungstic acid‐enhanced microCT: Optimized protocols for embryonic and early postnatal mice
KM Lesciotto, SM Motch Perrine, M Kawasaki, T Stecko, TM Ryan, ...
Developmental Dynamics 249 (4), 573-585, 2020
Mandates: US National Science Foundation, US National Institutes of Health
Tissue‐specific responses to aberrant FGF signaling in complex head phenotypes
N Martínez‐Abadías, SM Motch, TL Pankratz, Y Wang, K Aldridge, ...
Developmental Dynamics 242 (1), 80-94, 2013
Mandates: US National Institutes of Health, Government of Spain
p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice
Y Wang, X Zhou, K Oberoi, R Phelps, R Couwenhoven, M Sun, A Rezza, ...
The Journal of clinical investigation 122 (6), 2153-2164, 2012
Mandates: US National Institutes of Health
Overlapping trisomies for human chromosome 21 orthologs produce similar effects on skull and brain morphology of Dp (16) 1Yey and Ts65Dn mice
JM Starbuck, T Dutka, TS Ratliff, RH Reeves, JT Richtsmeier
American Journal of Medical Genetics Part A 164 (8), 1981-1990, 2014
Mandates: US National Institutes of Health, National Institute of Health and Medical …
The developmental basis of quantitative craniofacial variation in humans and mice
N Martínez-Abadías, P Mitteroecker, TE Parsons, M Esparza, T Sjøvold, ...
Evolutionary biology 39, 554-567, 2012
Mandates: US National Institutes of Health
Brain phenotypes in two FGFR2 mouse models for Apert syndrome
K Aldridge, CA Hill, JR Austin, C Percival, N Martinez‐Abadias, ...
Developmental dynamics: an official publication of the American Association …, 2010
Mandates: US National Institutes of Health
What are genes “for” or where are traits “from”? What is the question?
AV Buchanan, S Sholtis, J Richtsmeier, KM Weiss
Bioessays 31 (2), 198-208, 2009
Mandates: US National Institutes of Health
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