Zobrazeno 1 - 10
of 20
pro vyhledávání: '"P T, Jain"'
Publikováno v:
Indian Journal of Animal Sciences, Vol 92, Iss 6 (2022)
Animal cells are a valuable genetic resource and become the major tool for routine investigation of biological research and regenerative medicine. The somatic cells are as valuable as germ cells and an attractive resource for conserving animal geneti
Externí odkaz:
https://doaj.org/article/9e4c4881624446d49c88cca09f390709
Publikováno v:
HemaSphere, Vol 6, Pp 471-472 (2022)
Externí odkaz:
https://doaj.org/article/6339f76a1e2c4d90aa7f163ff93ba590
Publikováno v:
Astrophysics and Space Science. 368
Autor:
Bernhard Sattler, Mathias Kranz, Barbara Wenzel, Nalin T. Jain, Rareş-Petru Moldovan, Magali Toussaint, Winnie Deuther-Conrad, Friedrich-Alexander Ludwig, Rodrigo Teodoro, Tatjana Sattler, Masoud Sadeghzadeh, Osama Sabri, Peter Brust
Publikováno v:
Molecules, Vol 25, Iss 9, p 2024 (2020)
Overexpression of monocarboxylate transporters (MCTs) has been shown for a variety of human cancers (e.g., colon, brain, breast, and kidney) and inhibition resulted in intracellular lactate accumulation, acidosis, and cell death. Thus, MCTs are promi
Externí odkaz:
https://doaj.org/article/32254a7b8adf41b784ea0047efcc3021
Publikováno v:
Solar Physics. 297
Autor:
Y.-M. Di, David A. Gewirtz, N. C. Watson, Michael S. Orr, K. J. Magnet, P. T. Jain, Joyce K. Randolph, Frank A. Fornari
Publikováno v:
International Journal of Radiation Biology. 72:547-559
To determine the capacity of ionizing radiation to inhibit proliferation, to suppress c-myc expression and to induce apoptotic cell death in the p53 wild-type MCF-7 cell line and the p53 mutated MDA-MB231 cell line.Growth inhibition and cell killing
Publikováno v:
Anti-Cancer Drugs. 5:429-436
Compound 4d ((E)- and (Z)-1,1-Dichloro-2-[4-(benzyloxy)-phenyl]2,3-bis(4-methoxyphenyl) cyclopropane) and compound 5c ((Z)-1,1-Dichloro-2-[4-(benzyloxy)-phenyl]- 2-(4-methoxyphenyl)-3-phenylcyclopropane) are two members of a novel series of triarylcy
Publikováno v:
Breast Cancer Research and Treatment. 25:225-233
Compound 7a ([Z]-1,1,-dichloro-2,3-diphenyl-2-(4-(2-dimethylamino)ethoxy)phenyl) cyclopropane, dihydrogen citrate salt) is a novel cyclopropyl antiestrogen which was shown to be an estrogen antagonist without estrogen agonist activity. The antiprolif
Publikováno v:
ChemInform. 22
A series of 1,1-dichloro-2,2,3-triarylcyclopropanes (DTACs) was synthesized and evaluated as pure antiestrogens. Addition of 4-methoxy- or 4-(benzyloxy)phenyl Grignard reagents to p-methoxy, p-benzyloxy, or unsubstituted deoxybenzoins, followed by de
Publikováno v:
Journal of Medicinal Chemistry. 34:842-851
A series of 1,1-dichloro-2,2,3-triarylcyclopropanes (DTACs) was synthesized and evaluated as pure antiestrogens. Addition of 4-methoxy- or 4-(benzyloxy)phenyl Grignard reagents to p-methoxy, p-benzyloxy, or unsubstituted deoxybenzoins, followed by de