Zobrazeno 1 - 10
of 76
pro vyhledávání: '"L S, Kirschner"'
Autor:
L. S. Kirschner
Publikováno v:
Journal of Internal Medicine. 266:60-68
Carney complex (CNC) is an autosomal dominant, multiple endocrine neoplasia syndrome comprised of spotty skin pigmentation, myxomatosis, endocrine tumours and schwannomas. The majority of cases are due to inactivating mutations in PRKAR1A, the gene e
Autor:
Christian A. Koch, T. Nguyen, Edward Oldfield, P. K. Bryant-Greenwood, L. S. Kirschner, J A Carney, Constantine A. Stratakis, Joe C. Watson
Publikováno v:
Journal of Neurosurgery. 92:413-418
Object. The authors present their neurosurgical experience with Carney complex. Carney complex, characterized by spotty skin pigmentation, cardiac myxomas, primary pigmented nodular adrenocortical disease, pituitary tumors, and nerve sheath tumors (N
Autor:
L S Kirschner, C. A. Stratakis
Publikováno v:
Hormone and Metabolic Research. 30:456-463
Primary bilateral adrenocortical diseases are rare entities that have recently been appreciated as potential causes of Cushing syndrome. They include (i) primary pigmented adrenocortical disease (PPNAD), also known as "micronodular adrenal disease",
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(10)
Carney complex (CNC) is a familial multiple neoplasia and lentiginosis syndrome with features overlapping those of McCune-Albright syndrome (MAS) and other multiple endocrine neoplasia (MEN) syndromes, MEN type 1 (MEN 1), in particular. GH-producing
Autor:
L S, Kirschner, C A, Stratakis
Publikováno v:
BioTechniques. 27(1)
Publikováno v:
American journal of medical genetics. 80(2)
Autor:
C A, Stratakis, A, Vottero, A, Brodie, L S, Kirschner, D, DeAtkine, Q, Lu, W, Yue, C S, Mitsiades, A W, Flor, G P, Chrousos
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(4)
Increased extraglandular aromatization has been reported as the cause of familial gynecomastia. We studied a kindred with aromatase excess inherited in an autosomal dominant manner, in which affected males had heterosexual precocity and/or gynecomast
Publikováno v:
Cell growthdifferentiation : the molecular biology journal of the American Association for Cancer Research. 7(9)
The mdr2 gene is highly expressed in liver and is involved in the translocation of phospholipid. To study the regulation of mdr2 expression, the promoter of the mdr2 gene has been isolated from a murine vinblastine-resistant cell line, J7.V2-1, and c
Publikováno v:
WHO/IARC Classification of Tumours; 2017, Vol. 9, p269-271, 3p
Autor:
Ren, Jiang1 (AUTHOR), Yu, Peng2 (AUTHOR), Liu, Sijia3,4 (AUTHOR), Li, Ran1 (AUTHOR), Niu, Xin5 (AUTHOR), Chen, Yan1 (AUTHOR), Zhang, Zhenyu6 (AUTHOR) fcczhangzy1@zzu.edu.cn, Zhou, Fangfang7 (AUTHOR) zhoufangfang@suda.edu.cn, Zhang, Long1,3,5,8 (AUTHOR) l_zhang@zju.edu.cn
Publikováno v:
Advanced Science. 12/27/2023, Vol. 10 Issue 36, p1-37. 37p.