scholarly journals New insights into mullerian inhibiting substance and its mechanism of action

1998 ◽  
Vol 158 (1) ◽  
pp. 1-6 ◽  
Author(s):  
AH Lane ◽  
PK Donahoe

The primary function of MIS in mammals is to initiate regression of Mullerian structures in males as part of normal sexual development. As we learn more about its other roles, particularly its influence on the growth and differentiation of cell types within the gonad, a more thorough understanding of the receptors that MIS stimulates and the downstream signaling cascade with which it interacts will help in the development of diagnostic and therapeutic uses of MIS.

Cell ◽  
1994 ◽  
Vol 79 (3) ◽  
pp. 415-425 ◽  
Author(s):  
Richard R. Behringer ◽  
Milton J. Finegold ◽  
Richard L. Cate

1984 ◽  
Vol 46 (1) ◽  
pp. 53-65 ◽  
Author(s):  
P K Donahoe ◽  
J M Hutson ◽  
M E Fallat ◽  
S Kamagata ◽  
G P Budzik

Nature ◽  
1990 ◽  
Vol 345 (6271) ◽  
pp. 167-170 ◽  
Author(s):  
Richard R. Behringer ◽  
Richard L. Cate ◽  
Glenda J. Froelick ◽  
Richard D. Palmiter ◽  
Ralph L. Brinster

Author(s):  
PATRICIA K. DONAHOE ◽  
RICHARD L. CATE ◽  
DAVID T. MACLAUGHLIN ◽  
JAMES EPSTEIN ◽  
ARLAN F. FULLER ◽  
...  

2002 ◽  
Vol 89 (1) ◽  
pp. 113-118 ◽  
Author(s):  
J.E. Bartlett ◽  
S.M.Y. Lee ◽  
Y. Mishina ◽  
R.R. Behringer ◽  
N. Yang ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Kazunori Watanabe ◽  
Tomoko Nawachi ◽  
Ruriko Okutani ◽  
Takashi Ohtsuki

AbstractMethods to spatially induce apoptosis are useful for cancer therapy. To control the induction of apoptosis, methods using light, such as photochemical internalization (PCI), have been developed. We hypothesized that photoinduced delivery of microRNAs (miRNAs) that regulate apoptosis could spatially induce apoptosis. In this study, we identified pre-miR-664a as a novel apoptosis-inducing miRNA via mitochondrial apoptotic pathway. Further, we demonstrated the utility of photoinduced cytosolic dispersion of RNA (PCDR), which is an intracellular RNA delivery method based on PCI. Indeed, apoptosis is spatially regulated by pre-miR-664a and PCDR. In addition, we found that apoptosis induced by pre-miR-664a delivered by PCDR was more rapid than that by lipofection. These results suggest that pre-miR-664a is a nucleic acid drug candidate for cancer therapy and PCDR and pre-miR-664a-based strategies have potential therapeutic uses for diseases affecting various cell types.


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