Följ
Robert D Blank
Robert D Blank
Professor Emeritus of Medicine, Medical College of Wisconsin
Verifierad e-postadress på mcw.edu
Titel
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Collagen and bone strength
AL Boskey, TM Wright, RD Blank
Journal of Bone and Mineral Research 14 (3), 330-335, 1999
2621999
Secondary fracture prevention: consensus clinical recommendations from a multistakeholder coalition
RB Conley, G Adib, RA Adler, KE Åkesson, IM Alexander, KC Amenta, ...
Journal of bone and mineral research 35 (1), 36-52, 2020
2282020
Congenital and idiopathic scoliosis: clinical and genetic aspects
PF Giampietro, RD Blank, CL Raggio, S Merchant, FS Jacobsen, ...
Clinical Medicine & Research 1 (2), 125-136, 2003
1892003
Clinical, genetic and environmental factors associated with congenital vertebral malformations
PF Giampietro, CL Raggio, RD Blank, C McCarty, U Broeckel, MA Pickart
Molecular syndromology 4 (1-2), 94-105, 2013
1282013
An analysis of PAX1 in the development of vertebral malformations
PF Giampietro, CL Raggio, CE Reynolds, SK Shukla, E McPherson, ...
Clinical genetics 68 (5), 448-453, 2005
922005
A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups
D Londono, I Kou, TA Johnson, S Sharma, Y Ogura, T Tsunoda, ...
Journal of medical genetics 51 (6), 401-406, 2014
912014
Spontaneous recombinase activity of Cre–ERT2 in vivo
J Kristianto, MG Johnson, RK Zastrow, AB Radcliff, RD Blank
Transgenic research 26, 411-417, 2017
862017
Progress in the understanding of the genetic etiology of vertebral segmentation disorders in humans
PF Giampietro, SL Dunwoodie, K Kusumi, O Pourquié, O Tassy, AC Offiah, ...
Annals of the New York Academy of Sciences 1151 (1), 38-67, 2009
822009
A linkage map of mouse chromosome 12: localization of Igh and effects of sex and interference on recombination.
RD Blank, GR Campbell, A Calabro, P D'Eustachio
Genetics 120 (4), 1073-1083, 1988
821988
Osteoporosis in crisis: it's time to focus on fracture
N Binkley, RD Blank, WD Leslie, EM Lewiecki, JA Eisman, JP Bilezikian
Journal of Bone and Mineral Research 32 (7), 1391-1394, 2017
812017
Synteny‐defined candidate genes for congenital and idiopathic scoliosis
PF Giampietro, CL Raggio, RD Blank
American journal of medical genetics 83 (3), 164-177, 1999
801999
A novel locus for adolescent idiopathic scoliosis on chromosome 12p
CL Raggio, PF Giampietro, S Dobrin, C Zhao, D Dorshorst, ...
Journal of Orthopaedic Research 27 (10), 1366-1372, 2009
752009
Spectroscopically determined collagen Pyr/deH-DHLNL cross-link ratio and crystallinity indices differ markedly in recombinant congenic mice with divergent calculated bone …
RD Blank, TH Baldini, M Kaufman, S Bailey, R Gupta, Y Yershov, ...
Connective tissue research 44 (3-4), 134-142, 2003
742003
A Missense T(Brachyury) Mutation Contributes to Vertebral Malformations
N Ghebranious, RD Blank, CL Raggio, J Staubli, E McPherson, L Ivacic, ...
Journal of bone and mineral research 23 (10), 1576-1583, 2008
732008
Clinical value of monitoring BMD in patients treated with bisphosphonates for osteoporosis
NB Watts, EM Lewiecki, SL Bonnick, AJ Laster, N Binkley, RD Blank, ...
Journal of Bone and Mineral Research 24 (10), 1643-1646, 2009
722009
Induced ablation of Bmp1 and Tll1 produces osteogenesis imperfecta in mice
AM Muir, Y Ren, DH Butz, NA Davis, RD Blank, DE Birk, SJ Lee, D Rowe, ...
Human molecular genetics 23 (12), 3085-3101, 2014
712014
Advances in the nutritional and pharmacological management of phenylketonuria
DM Ney, RD Blank, KE Hansen
Current Opinion in Clinical Nutrition & Metabolic Care 17 (1), 61-68, 2014
712014
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene …
J Liu, N Wu, ...
Genetics in Medicine 21 (7), 1548-1558, 2019
632019
Hexa‐D‐arginine treatment increases 7B2•PC2 activity in hyp‐mouse osteoblasts and rescues the HYP phenotype
B Yuan, JQ Feng, S Bowman, Y Liu, RD Blank, I Lindberg, MK Drezner
Journal of bone and mineral research 28 (1), 56-72, 2013
622013
Low bone strength is a manifestation of phenylketonuria in mice and is attenuated by a glycomacropeptide diet
P Solverson, SG Murali, SJ Litscher, RD Blank, DM Ney
Public Library of Science 7 (9), e45165, 2012
592012
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Artiklar 1–20