Dwarfism Research Today is a free monthly online journal that collates and summarizes the latest research about Dwarfism, including details on genetics, diet, mental and motor development.

Volume 7 (2011), Issue 10 (October)

1. Recent advances in understanding plant Myosin function: life in the fast lane.
   Mol Plant, 4(5): 805-12. [Abstract] [Full-text]
2. Reciprocally regulated chromatin association of Cockayne syndrome protein B and p53 protein.
   J Biol Chem, 286(40): 34951-8. [Abstract] [Full-text]
3. Antisense Suppression of the Small Chloroplast Protein CP12 in Tobacco Alters Carbon Partitioning and Severely Restricts Growth.
   Plant Physiol, 157(2): 620-31. [Abstract] [Full-text]
4. Antisense suppression of the small chloroplast protein CP12 in tobacco alters carbon partitioning and severely restricts growth.
   Plant Physiol, 157(2): 620-31. [Abstract] [Full-text]
5. Catecholaminergic axonal varicosities appear to innervate growth hormone-releasing hormone-immunoreactive neurons in the human hypothalamus: the possible morphological substrate of the stress-suppressed growth.
   J Clin Endocrinol Metab, 96(10): E1606-11. [Abstract] [Full-text]
6. Approach to the diagnosis and treatment of neonatal hypothyroidism.
   J Clin Endocrinol Metab, 96(10): 2959-67. [Abstract] [Full-text]
7. Catecholaminergic axonal varicosities appear to innervate growth hormone-releasing hormone-immunoreactive neurons in the human hypothalamus: the possible morphological substrate of the stress-suppressed growth.
   J Clin Endocrinol Metab, 96(10): E1606-11. [Abstract] [Full-text]
8. Molecular screening of the TSH receptor (TSHR) and thyroid peroxidase (TPO) genes in Korean patients with nonsyndromic congenital hypothyroidism.
   Clin Endocrinol (Oxf), 75(5): 715-21. [Abstract] [Full-text]
9. Mechanisms and pathways of growth failure in primordial dwarfism.
   Genes Dev, 25(19): 2011-24. [Abstract] [Full-text]
10. Mechanisms and pathways of growth failure in primordial dwarfism.
    Genes Dev, 25(19): 2011-24. [Abstract] [Full-text]
11. Growth hormone: the expansion of available products and indications.
    Pediatr Clin North Am, 58(5): 1141-65, x. [Abstract] [Full-text]
12. Congenital disorders of the thyroid: hypo/hyper.
    Pediatr Clin North Am, 58(5): 1099-115, ix. [Abstract] [Full-text]
13. The role of the SHOX gene in the pathophysiology of Turner syndrome.
    Endocrinol Nutr, 58(8): 433-42. [Abstract] [Full-text]
14. Exercise-induced GH secretion in the assessment of GH deficiency in adult individuals.
    Eur J Endocrinol, 165(5): 723-8. [Abstract] [Full-text]
15. ATELOSTEOGENESIS TYPE I; AUTOPSY FINDINGS.
    Pediatr Dev Pathol. [Abstract] [Full-text]
16. Are pregnant women in New Zealand iodine deficient? A cross-sectional survey.
    Aust N Z J Obstet Gynaecol, 51(5): 464-7. [Abstract] [Full-text]
17. Testing of buccal swab DNA does not increase the detection rate for imprinting control region 1 hypomethylation in Silver-Russell syndrome.
    Genet Test Mol Biomarkers, 15(10): 725-6. [Abstract] [Full-text]
18. CtIP Mutations Cause Seckel and Jawad Syndromes.
    PLoS Genet, 7(10): e1002310. [Abstract] [Full-text]
19. Ligand activation leads to regulated intramembrane proteolysis of fibroblast growth factor receptor 3.
    Mol Biol Cell, 22(20): 3861-73. [Abstract] [Full-text]
20. CtIP Mutations Cause Seckel and Jawad Syndromes.
    PLoS Genet, 7(10): e1002310. [Abstract] [Full-text]
21. Ligand activation leads to regulated intramembrane proteolysis of fibroblast growth factor receptor 3.
    Mol Biol Cell, 22(20): 3861-73. [Abstract] [Full-text]
22. Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis.
    Arch Dis Child Fetal Neonatal Ed, 96(6): F453-6. [Abstract] [Full-text]
23. Correlates of low bone mass in children with generalized forms of epidermolysis bullosa.
    J Am Acad Dermatol, 65(5): 1001-9. [Abstract] [Full-text]
24. A novel form of chondrocyte stress is triggered by a COMP mutation causing pseudoachondroplasia.
    Hum Mutat. [Abstract] [Full-text]
25. Dominant and pleiotropic effects of a GAI gene in wheat results from lack of interaction between DELLA and GID1.
    Plant Physiol. [Abstract] [Full-text]
26. Inducible nitric oxide synthase-nitric oxide signaling mediates the mitogenic activity of Rac1 during endochondral bone growth.
    J Cell Sci, 124: 3405-13. [Abstract] [Full-text]
27. Anaesthetic management of a parturient with Laron syndrome.
    Int J Obstet Anesth, 20(4): 344-6. [Abstract] [Full-text]
28. Sulfate in fetal development.
    Semin Cell Dev Biol, 22(6): 653-9. [Abstract] [Full-text]
29. Inducible nitric oxide synthase-nitric oxide signaling mediates the mitogenic activity of Rac1 during endochondral bone growth.
    J Cell Sci, 124: 3405-13. [Abstract] [Full-text]
30. Anaesthetic management of a parturient with Laron syndrome.
    Int J Obstet Anesth, 20(4): 344-6. [Abstract] [Full-text]
31. Molecular characterisation of Rht-1 dwarfing genes in hexaploid wheat (Triticum aestivum).
    Plant Physiol. [Abstract] [Full-text]
32. Desbuquois dysplasia type I and fetal hydrops due to novel mutations in the CANT1 gene.
    Eur J Hum Genet, 19(11): 1133-7. [Abstract] [Full-text]
33. Diagnosis and treatment of subclinical hypothyroidism detected by neonatal screening.
    World J Pediatr, 7(4): 350-4. [Abstract] [Full-text]
34. A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder.
    Am J Med Genet A, 155(11): 2885-96. [Abstract] [Full-text]
35. Insertional mutation in the Golgb1 gene is associated with osteochondrodysplasia and systemic edema in the OCD rat.
    Bone, 49(5): 1027-36. [Abstract] [Full-text]
36. A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder.
    Am J Med Genet A, 155(11): 2885-96. [Abstract] [Full-text]
37. Insertional mutation in the Golgb1 gene is associated with osteochondrodysplasia and systemic edema in the OCD rat.
    Bone, 49(5): 1027-36. [Abstract] [Full-text]
38. Nonsense-mediated mRNA decay factors, UPF1 and UPF3, contribute to plant defense.
    Plant Cell Physiol. [Abstract] [Full-text]
39. The Centrosomal Protein Pericentrin Identified at the Basal Body Complex of the Connecting Cilium in Mouse Photoreceptors.
    PLoS One, 6(10): e26496. [Abstract] [Full-text]
40. The centrosomal protein pericentrin identified at the basal body complex of the connecting cilium in mouse photoreceptors.
    PLoS One, 6(10): e26496. [Abstract] [Full-text]
41. Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: identification a cryptic donor splice site in the exon 19.
    Mol Cell Endocrinol, 348(1): 313-21. [Abstract] [Full-text]
42. Long-term safety and efficacy of the recombinant human growth hormone Omnitrope® in the treatment of Spanish growth hormone deficient children: results of a phase III study.
    Adv Ther, 28(10): 879-93. [Abstract] [Full-text]
43. The Aarskog-Scott syndrome protein Fgd1 regulates podosome formation and extracellular matrix remodeling in transforming growth factor β-stimulated aortic endothelial cells.
    Mol Cell Biol, 31(22): 4430-41. [Abstract] [Full-text]

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