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Myths and variations in normal pubertal development.
Nakamoto JM. Nakamoto JM. West J Med. 2000 Mar;172(3):182-5. doi: 10.1136/ewjm.172.3.182. West J Med. 2000. PMID: 10734809 Free PMC article. Review. No abstract available.
Minipuberty of infancy and adolescent pubertal function in adrenal hypoplasia congenita.
Kaiserman KB, Nakamoto JM, Geffner ME, McCabe ER. Kaiserman KB, et al. Among authors: nakamoto jm. J Pediatr. 1998 Aug;133(2):300-2. doi: 10.1016/s0022-3476(98)70242-2. J Pediatr. 1998. PMID: 9709728
DAX1 mutations map to putative structural domains in a deduced three-dimensional model.
Zhang YH, Guo W, Wagner RL, Huang BL, McCabe L, Vilain E, Burris TP, Anyane-Yeboa K, Burghes AH, Chitayat D, Chudley AE, Genel M, Gertner JM, Klingensmith GJ, Levine SN, Nakamoto J, New MI, Pagon RA, Pappas JG, Quigley CA, Rosenthal IM, Baxter JD, Fletterick RJ, McCabe ER. Zhang YH, et al. Among authors: nakamoto j. Am J Hum Genet. 1998 Apr;62(4):855-64. doi: 10.1086/301782. Am J Hum Genet. 1998. PMID: 9529340 Free PMC article.
Conventional and nonconventional uses of growth hormone.
Lippe BM, Nakamoto JM. Lippe BM, et al. Among authors: nakamoto jm. Recent Prog Horm Res. 1993;48:179-235. doi: 10.1016/b978-0-12-571148-7.50011-7. Recent Prog Horm Res. 1993. PMID: 8441848 Review.
Prevalence of three mutations in the Gs alpha gene among 24 families with pseudohypoparathyroidism type Ia.
Lin CK, Hakakha MJ, Nakamoto JM, Englund AT, Brickman AS, Scott ML, Van Dop C. Lin CK, et al. Among authors: nakamoto jm. Biochem Biophys Res Commun. 1992 Nov 30;189(1):343-9. doi: 10.1016/0006-291x(92)91564-7. Biochem Biophys Res Commun. 1992. PMID: 1449489
Concurrent hormone resistance (pseudohypoparathyroidism type Ia) and hormone independence (testotoxicosis) caused by a unique mutation in the G alpha s gene.
Nakamoto JM, Zimmerman D, Jones EA, Loke KY, Siddiq K, Donlan MA, Brickman AS, Van Dop C. Nakamoto JM, et al. Biochem Mol Med. 1996 Jun;58(1):18-24. doi: 10.1006/bmme.1996.0027. Biochem Mol Med. 1996. PMID: 8809352
Pseudohypoparathyroidism type Ia from maternal but not paternal transmission of a Gsalpha gene mutation.
Nakamoto JM, Sandstrom AT, Brickman AS, Christenson RA, Van Dop C. Nakamoto JM, et al. Am J Med Genet. 1998 May 26;77(4):261-7. Am J Med Genet. 1998. PMID: 9600732
Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS.
Bastepe M, Fröhlich LF, Hendy GN, Indridason OS, Josse RG, Koshiyama H, Körkkö J, Nakamoto JM, Rosenbloom AL, Slyper AH, Sugimoto T, Tsatsoulis A, Crawford JD, Jüppner H. Bastepe M, et al. Among authors: nakamoto jm. J Clin Invest. 2003 Oct;112(8):1255-63. doi: 10.1172/JCI19159. J Clin Invest. 2003. PMID: 14561710 Free PMC article.
Resources for molecular biology.
Nakamoto J. Nakamoto J. Nat Biotechnol. 1998 Sep;16(9):879. doi: 10.1038/nbt0998-879. Nat Biotechnol. 1998. PMID: 9743125 No abstract available.
Use of in vitro clonogenic assays to differentiate acquired from genetic causes of insulin resistance.
Geffner ME, Bersch N, Nakamoto JM, Scott M, Johnson NB, Golde DW. Geffner ME, et al. Among authors: nakamoto jm. Diabetes. 1991 Jan;40(1):28-36. doi: 10.2337/diab.40.1.28. Diabetes. 1991. PMID: 1849848
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