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Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46
RESEARCH ARTICLE

www.ijera.com

OPEN ACCESS

A MathematicaL Model For Finding Maximum Likelihood
Estimator Functions of Luteinizing Hormone, Follicle
Stimulating Hormone, Estradiol and Progesterone.
Dr,S.Lakshmi * and M.Agalya**
*Principal, Govt.Arts and Science College, Peravurani ,Thanjavur Dist.
** Research Scholar, PG& Research Department of Mathematics, K.N. Govt.Arts College for
Women,Thanjavur.
ABSTRACT
The Corpus luteum is formed by the action of luteinizing hormone (LH) on the mature preovulatory follicle.
Ensuing events, including steroidogenic outpouring, programmed senescence, and capacity for extension by
gestation, depend on features characteristic of an adequately developed preovulatory follicle, including, most
importantly, the number and LH, Follicle stimulating hormone (FSH) ,Estradiol (E2), and progesterone (P). The
Maximum likelihood functions are obtained for the above medical variables before and after infusion of LH
surge ,which are well explained by mathematical figures in the section [3].

Keywords: MLE, LH , FSH, E2, P.
Mathematical Classification: 60GXX, 60E05

I.

Mathematical Model

M/M/1/N queuing model for the secretion of DHEA due to human stress, is developed by Lakshmi.S and
Geetharani.B [12].Stochastic Model for endocrine stress responses in chronic fatigue syndrome , is developed
by Lakshmi.S and Shanmugapriya.S [13] .A Mathematical model for finding the Association of Thyroid
Stimulating hormone with LH and FSH is developed by Lakshmi.S and Agalya.M.[11].Here we have obtained
Maximum likelihood Estimator function for the medical variables LH,FSH, Estradiol and Progesterone.
Let x1 , x2, x3, ….. xn be a random sample from a normal distribution N(μ,σ ) [4,9,13,15].
The likelihood function of (μ,σ ) is

1

L(μ,σ ;X ) =

exp ( -

1
(2 )

n/2

2

2

 (x   )

2

i

(2 ) 
1 n
1
( x -x )2
exp ( n
2
i

2 i 1
n

n/2

=

n

1

i 1

)

-

1 n
( x   ) 2 ) …….(1)
2
2

- ∞ < μ < ∞ , 0 < σ < ∞. It follows immediately that the likelihood function is maximized, for each value of



σ , by
Where
Let

Q

x

x

=
n

n

is the sample mean.

n

n

n

=


i 1

L(



(

x - x ) 2 . Substituting
i

,σ ; x ) =
n

1
(2 )

exp ( -



n/2

n



in (1) ,we obtain
n

1
2

2

Q

n

).

………….(2)

Hence ,

www.ijera.com

41 | P a g e
Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46

www.ijera.com


n Qn
in L(  ,σ ; x ) = - +
.
3
n
x




Equating this partial derivative to zero and solving for σ ,we obtain the Maximum likelihood Estimator MLE
[10]


Thus ,the MLE of (μ ,σ ) is (

n

= (

Q

 ,
n

n 1/2

)

n
n

=

(

1
n

n


i 1

(

x - x ) 2 )1/2
i

.

).

II.
Application
The Corpus luteum is a remarkable, transiently functioning organ that provides the endocrine
conditions that are necessary and sufficient for the establishment and maintenance of early pregnancy. On a
weight basis, it is the most productive steroid-secreting tissue in the body. It is abruptly formed from the
remnants of the preovulatory follicle, and it undergoes continuous change thereafter.
The corpus luteum is formed by the action of luteinizing hormone (LH) on the mature preovulatory
follicle. Ensuing events, including steroidogenic outpouring, programmed senescence, and capacity for
extension by gestation, depend on features characteristic of an adequately developed preovulatory follicle,
including, most importantly, the number and LH receptivity of the granulosa cell population, both of which are
follicle-stimulating hormone (FSH)–dependent properties. Acquisition of LH receptor (LHR) by preovulatory
granulosa cells results from estrogen-stimulated and FSH-stimulated transcription of the LHR gene, the actions
of which are mediated largely by intracellullar cyclic adenosine monophosphate (cAMP)[16]. Actions of LH
and human chorionic gonadotropin (hCG) define the functional unfolding of luteal events and are thought to be
exclusively dependent on activation of this single, G-protein–coupled receptor.
LHR-mediated effects occur primarily via the Gs / adenylyl cyclase / cAMP / PKA signaling pathway,
although evidence for activation of other signaling pathways (e.g., inositol phosphate pathway) and possible
roles for these is accumulating [2]. The luteotropic action of LH or hCG on follicles that are not mature can
produce luteinization of the theca, where LHRs are present, but does not set in motion the distinctive sequence
of changes in morphology and function of the granulosa and theca that characterize the corpus luteum.
In ovulatory cycles, there is an increase in progesterone levels that begins before the LH surge, thought
possibly to contribute to the positive feedback signal for pituitary release of LH (Fig-1). This harbinger of luteal
function is accompanied by a preovulatory increase in circulating 17-hydroxyprogesterone, the levels over time
of which differ in pattern from those of progesterone by decreasing after the LH peak, in contrast to the rapid
postovulatory increase in progesterone levels. These events may reveal an innate tendency for the granulosa
cells of the mature follicle to secrete progestins, as occurs spontaneously when such cells are studied in vitro
without an LH signal.
They foretell the remarkable increase in the overall rate of steroidogenesis that soon will be underway:
In a few days, the steroidogenic output of the ovary increases from a few hundred micrograms of estrogen to 20
mg or more of progesterone daily—a 100-fold increase. Ovulation marks a shift in inhibin production from the
inhibin B dominance of the follicular phase to predominant production of inhibin A, the levels of which roughly
parallel steroid secretion by the corpus luteum. Late follicular phase granulosa cells elaborate alpha subunit and
beta (B) subunit mRNA in response to FSH and LH.

www.ijera.com

42 | P a g e
Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46

www.ijera.com

Hours
Fig. 1. Mean (± SE) luteinizing hormone, follicle-stimulating hormone, estradiol, and progesterone levels over 5
days at mid cycle in seven studies in five subjects. The data are centered on the luteinizing hormone surge. Progesterone
levels rise in several phases—before, during, and after the luteinizing hormone surge.

The increase in steroidogenesis in the periovulatory period is accompanied by granulosa cell
proliferation and considerable functional and structural reorganization that eventuate in the distinct morphology
of the corpus luteum. Expression of the transcription factor early growth response factor-1, known as a
coordinator for multiple transcriptional alterations in circumstances of tissue change, is induced in human
granulosa cells by hCG. Expression of this growth factor also is stimulated by cholinergic activation of
muscarinic receptors on granulosa cells[7]. Activation of muscarinic receptors also blocks gap junctions via
phosphorylation of connexins therein and stimulates cell proliferation via increases in intracellular calcium,
together suggesting that cholinergic mechanisms may participate in the rapid reprogramming of granulosa cells
in the periovulatory period [8].

www.ijera.com

43 | P a g e
Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46
III.

www.ijera.com

Mathematical Results:

Maximum likelihood Function
6
5
4
3

Before FSH

2

Before LH

1
0
1

3

5

7

9

11 13 15 17 19 21

Maximum likelihood Function
14
12
10
A

8
After FSH

6

After LH

4
2
0
1

www.ijera.com

3

5

7

9

11

13

15

17

19

21

44 | P a g e
Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46

www.ijera.com

Maximum likelihood Function
8
7
6
5
4

Before Progesterone

3

Before Estradiol

2
1
0
1

3

5

7

9 11 13 15 17 19 21 23

Maximum likelihood Function
12
10
8
6

After Progesterone

4

After Estradiol

2
0
1

3

5

7

9 11 13 15 17 19 21 23

From the Mathematical results we have obtained the following results:
i) Before infusion of LH surge, LH ,FSH are gradually increasing
ii) Before infusion of LH surge, E2, and P are gradually increasing
ii) After infusion of LH Surge, LH and FSH increasing and then gradually decreasing
iii) After infusion of LH Surge, Progesterone increasing gradually but Estradiol suddenly decreases.

IV.

Conclusion

The increase in steroidogenesis in the periovulatory period is accompanied by granulose cell
proliferation and considerable functional and structural reorganization that eventuate in the distinct morphology
of the corpus luteum. The maximum likelihood functions have been obtained and analysed for all the four
variables before and after of LH Surge in the corresponding mathematical figures in section [3].

[1.]

[2.]
[3.]

References
Arthur ID, Anthony FW, Adams S, Thomas EJ: Serum relaxin and the major endometrial secretory
proteins in in-vitro fertilization and down-regulated hormone-supported and natural cycle frozen
embryo transfer. Hum Reprod 11:88, 1996.
Ascoli M, Fanelli F, Segaloff DL: The lutropin / Choriogonadotropin receptor, a 2002 perspective.
Endocr Rev 23:141,2002.
Balasch J, Creus M, Fabregues F, et al: Midluteal immunoreactive alpha inhibin serum concentrations
as markers of luteal phase deficiency. Hum Reprod 11:2591, 1996

www.ijera.com

45 | P a g e
Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46
[4.]
[5.]
[6.]
[7.]

[8.]
[9.]

[10.]
[11.]

[12.]
[13.]
[14.]

[15.]
[16.]

www.ijera.com

Barlow,R.E and Proschan, F., Mathemmatical Theory of Reliability , John wiley ,New York ,1965
Advanced mathematical treatment of maintenance policies and redundancy optimization
Bennegard B, Hahlin M, Hamberger L: Luteotrophic effects of prostaglandins I2 and D2 on isolated
human corpus luteum. Fertil Steril 54:459, 1990.
Devoto L, Kohen P, Gonzalez RR, et al: Expression of steroidogenic acute regulatory protein in the
human corpus luteum throughout the luteal phase. J Clin Endocrinol Metab 86:5633, 2001.
Fritz S, Kunz L, Dimitrijevi N, et al: Muscarine receptors in human luteinized granulose cells:
Activation blocks gap junctions and induces the transcription factor early growth response factor- 1.
J Clin Endocrinol Metab 87:1362,2002.
Fritz S, Wessler I, Breitling R, et al : Expression of muscarinic receptor types in the primate ovary and
evidence for non-neuronal acetylcholine synthesis. J Clin Endocrinol Metab 86:349,2001.
Good, I.J., The Estimation of probability : An essay on Modern Bayseian Methods, MIT
press ,Cambridge,MA,1965. Skillfully written introduction to Bayesian estimation of probabilities and
distriubution.
Hald,A., Maximum Likelihood estimation of the parameter of a normal distribution which is truncated
at a known point, Skandinavisk Aktuar., 32:119-134 (1949).
Lakshmi,S and Agalya,M., A Mathematical model for finding the Association of Thyroid Stimulating
hormone with LH and FSH ,International Journal of Mathematical Sciences Vol-13,No.1-2.P-8593,2014.
Lakshmi,S and Geetharani,B.,M/M/1/N queuing model for the secretion of DHEA due to human
stress, Bioscience Research Bulletrin Vol-26,Issue No.2,2010,PP:123-129.
Lakshmi,S and Shanmugapriya,S ,Stochastic Model for endocrine stress responses in chronic fatigue
syndrome ,Bioscience Research Bulletin V0l-24,No-2,2008,P-63-67.
Martz,H.F. and Waller, R.A., Bayesian Reliability Analysis, John Wiley, New York,1982.The book
contains important information for Bayesian analysis in Reliability theory, including a good chapter on
empirical Bayes methods.
Miller ,R.G., Jr., Survival Analysis ,John Wiley,New York,1981.Treats mainly non –parametric
methods in aconcise manner.
Shi H, Segaloff DL : A role for increased lutropin/ choriogondotropin receptor (LHR) gene
transcription in the follitropin –stimulated induction of the LHR in granulose cells. Mol
Endocrinol
9: 734,1995.

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46 | P a g e

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  • 1. Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46 RESEARCH ARTICLE www.ijera.com OPEN ACCESS A MathematicaL Model For Finding Maximum Likelihood Estimator Functions of Luteinizing Hormone, Follicle Stimulating Hormone, Estradiol and Progesterone. Dr,S.Lakshmi * and M.Agalya** *Principal, Govt.Arts and Science College, Peravurani ,Thanjavur Dist. ** Research Scholar, PG& Research Department of Mathematics, K.N. Govt.Arts College for Women,Thanjavur. ABSTRACT The Corpus luteum is formed by the action of luteinizing hormone (LH) on the mature preovulatory follicle. Ensuing events, including steroidogenic outpouring, programmed senescence, and capacity for extension by gestation, depend on features characteristic of an adequately developed preovulatory follicle, including, most importantly, the number and LH, Follicle stimulating hormone (FSH) ,Estradiol (E2), and progesterone (P). The Maximum likelihood functions are obtained for the above medical variables before and after infusion of LH surge ,which are well explained by mathematical figures in the section [3]. Keywords: MLE, LH , FSH, E2, P. Mathematical Classification: 60GXX, 60E05 I. Mathematical Model M/M/1/N queuing model for the secretion of DHEA due to human stress, is developed by Lakshmi.S and Geetharani.B [12].Stochastic Model for endocrine stress responses in chronic fatigue syndrome , is developed by Lakshmi.S and Shanmugapriya.S [13] .A Mathematical model for finding the Association of Thyroid Stimulating hormone with LH and FSH is developed by Lakshmi.S and Agalya.M.[11].Here we have obtained Maximum likelihood Estimator function for the medical variables LH,FSH, Estradiol and Progesterone. Let x1 , x2, x3, ….. xn be a random sample from a normal distribution N(μ,σ ) [4,9,13,15]. The likelihood function of (μ,σ ) is 1 L(μ,σ ;X ) = exp ( - 1 (2 ) n/2 2 2  (x   ) 2 i (2 )  1 n 1 ( x -x )2 exp ( n 2 i  2 i 1 n n/2 = n 1 i 1 ) - 1 n ( x   ) 2 ) …….(1) 2 2 - ∞ < μ < ∞ , 0 < σ < ∞. It follows immediately that the likelihood function is maximized, for each value of  σ , by Where Let Q x x = n n is the sample mean. n n n =  i 1 L(  ( x - x ) 2 . Substituting i ,σ ; x ) = n 1 (2 ) exp ( -  n/2 n  in (1) ,we obtain n 1 2 2 Q n ). ………….(2) Hence , www.ijera.com 41 | P a g e
  • 2. Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46 www.ijera.com  n Qn in L(  ,σ ; x ) = - + . 3 n x   Equating this partial derivative to zero and solving for σ ,we obtain the Maximum likelihood Estimator MLE [10]  Thus ,the MLE of (μ ,σ ) is ( n = ( Q  , n n 1/2 ) n n = ( 1 n n  i 1 ( x - x ) 2 )1/2 i . ). II. Application The Corpus luteum is a remarkable, transiently functioning organ that provides the endocrine conditions that are necessary and sufficient for the establishment and maintenance of early pregnancy. On a weight basis, it is the most productive steroid-secreting tissue in the body. It is abruptly formed from the remnants of the preovulatory follicle, and it undergoes continuous change thereafter. The corpus luteum is formed by the action of luteinizing hormone (LH) on the mature preovulatory follicle. Ensuing events, including steroidogenic outpouring, programmed senescence, and capacity for extension by gestation, depend on features characteristic of an adequately developed preovulatory follicle, including, most importantly, the number and LH receptivity of the granulosa cell population, both of which are follicle-stimulating hormone (FSH)–dependent properties. Acquisition of LH receptor (LHR) by preovulatory granulosa cells results from estrogen-stimulated and FSH-stimulated transcription of the LHR gene, the actions of which are mediated largely by intracellullar cyclic adenosine monophosphate (cAMP)[16]. Actions of LH and human chorionic gonadotropin (hCG) define the functional unfolding of luteal events and are thought to be exclusively dependent on activation of this single, G-protein–coupled receptor. LHR-mediated effects occur primarily via the Gs / adenylyl cyclase / cAMP / PKA signaling pathway, although evidence for activation of other signaling pathways (e.g., inositol phosphate pathway) and possible roles for these is accumulating [2]. The luteotropic action of LH or hCG on follicles that are not mature can produce luteinization of the theca, where LHRs are present, but does not set in motion the distinctive sequence of changes in morphology and function of the granulosa and theca that characterize the corpus luteum. In ovulatory cycles, there is an increase in progesterone levels that begins before the LH surge, thought possibly to contribute to the positive feedback signal for pituitary release of LH (Fig-1). This harbinger of luteal function is accompanied by a preovulatory increase in circulating 17-hydroxyprogesterone, the levels over time of which differ in pattern from those of progesterone by decreasing after the LH peak, in contrast to the rapid postovulatory increase in progesterone levels. These events may reveal an innate tendency for the granulosa cells of the mature follicle to secrete progestins, as occurs spontaneously when such cells are studied in vitro without an LH signal. They foretell the remarkable increase in the overall rate of steroidogenesis that soon will be underway: In a few days, the steroidogenic output of the ovary increases from a few hundred micrograms of estrogen to 20 mg or more of progesterone daily—a 100-fold increase. Ovulation marks a shift in inhibin production from the inhibin B dominance of the follicular phase to predominant production of inhibin A, the levels of which roughly parallel steroid secretion by the corpus luteum. Late follicular phase granulosa cells elaborate alpha subunit and beta (B) subunit mRNA in response to FSH and LH. www.ijera.com 42 | P a g e
  • 3. Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46 www.ijera.com Hours Fig. 1. Mean (± SE) luteinizing hormone, follicle-stimulating hormone, estradiol, and progesterone levels over 5 days at mid cycle in seven studies in five subjects. The data are centered on the luteinizing hormone surge. Progesterone levels rise in several phases—before, during, and after the luteinizing hormone surge. The increase in steroidogenesis in the periovulatory period is accompanied by granulosa cell proliferation and considerable functional and structural reorganization that eventuate in the distinct morphology of the corpus luteum. Expression of the transcription factor early growth response factor-1, known as a coordinator for multiple transcriptional alterations in circumstances of tissue change, is induced in human granulosa cells by hCG. Expression of this growth factor also is stimulated by cholinergic activation of muscarinic receptors on granulosa cells[7]. Activation of muscarinic receptors also blocks gap junctions via phosphorylation of connexins therein and stimulates cell proliferation via increases in intracellular calcium, together suggesting that cholinergic mechanisms may participate in the rapid reprogramming of granulosa cells in the periovulatory period [8]. www.ijera.com 43 | P a g e
  • 4. Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46 III. www.ijera.com Mathematical Results: Maximum likelihood Function 6 5 4 3 Before FSH 2 Before LH 1 0 1 3 5 7 9 11 13 15 17 19 21 Maximum likelihood Function 14 12 10 A 8 After FSH 6 After LH 4 2 0 1 www.ijera.com 3 5 7 9 11 13 15 17 19 21 44 | P a g e
  • 5. Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46 www.ijera.com Maximum likelihood Function 8 7 6 5 4 Before Progesterone 3 Before Estradiol 2 1 0 1 3 5 7 9 11 13 15 17 19 21 23 Maximum likelihood Function 12 10 8 6 After Progesterone 4 After Estradiol 2 0 1 3 5 7 9 11 13 15 17 19 21 23 From the Mathematical results we have obtained the following results: i) Before infusion of LH surge, LH ,FSH are gradually increasing ii) Before infusion of LH surge, E2, and P are gradually increasing ii) After infusion of LH Surge, LH and FSH increasing and then gradually decreasing iii) After infusion of LH Surge, Progesterone increasing gradually but Estradiol suddenly decreases. IV. Conclusion The increase in steroidogenesis in the periovulatory period is accompanied by granulose cell proliferation and considerable functional and structural reorganization that eventuate in the distinct morphology of the corpus luteum. The maximum likelihood functions have been obtained and analysed for all the four variables before and after of LH Surge in the corresponding mathematical figures in section [3]. [1.] [2.] [3.] References Arthur ID, Anthony FW, Adams S, Thomas EJ: Serum relaxin and the major endometrial secretory proteins in in-vitro fertilization and down-regulated hormone-supported and natural cycle frozen embryo transfer. Hum Reprod 11:88, 1996. Ascoli M, Fanelli F, Segaloff DL: The lutropin / Choriogonadotropin receptor, a 2002 perspective. Endocr Rev 23:141,2002. Balasch J, Creus M, Fabregues F, et al: Midluteal immunoreactive alpha inhibin serum concentrations as markers of luteal phase deficiency. Hum Reprod 11:2591, 1996 www.ijera.com 45 | P a g e
  • 6. Dr,S.Lakshmi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 2( Version 4), February 2014, pp.41-46 [4.] [5.] [6.] [7.] [8.] [9.] [10.] [11.] [12.] [13.] [14.] [15.] [16.] www.ijera.com Barlow,R.E and Proschan, F., Mathemmatical Theory of Reliability , John wiley ,New York ,1965 Advanced mathematical treatment of maintenance policies and redundancy optimization Bennegard B, Hahlin M, Hamberger L: Luteotrophic effects of prostaglandins I2 and D2 on isolated human corpus luteum. Fertil Steril 54:459, 1990. Devoto L, Kohen P, Gonzalez RR, et al: Expression of steroidogenic acute regulatory protein in the human corpus luteum throughout the luteal phase. J Clin Endocrinol Metab 86:5633, 2001. Fritz S, Kunz L, Dimitrijevi N, et al: Muscarine receptors in human luteinized granulose cells: Activation blocks gap junctions and induces the transcription factor early growth response factor- 1. J Clin Endocrinol Metab 87:1362,2002. Fritz S, Wessler I, Breitling R, et al : Expression of muscarinic receptor types in the primate ovary and evidence for non-neuronal acetylcholine synthesis. J Clin Endocrinol Metab 86:349,2001. Good, I.J., The Estimation of probability : An essay on Modern Bayseian Methods, MIT press ,Cambridge,MA,1965. Skillfully written introduction to Bayesian estimation of probabilities and distriubution. Hald,A., Maximum Likelihood estimation of the parameter of a normal distribution which is truncated at a known point, Skandinavisk Aktuar., 32:119-134 (1949). Lakshmi,S and Agalya,M., A Mathematical model for finding the Association of Thyroid Stimulating hormone with LH and FSH ,International Journal of Mathematical Sciences Vol-13,No.1-2.P-8593,2014. Lakshmi,S and Geetharani,B.,M/M/1/N queuing model for the secretion of DHEA due to human stress, Bioscience Research Bulletrin Vol-26,Issue No.2,2010,PP:123-129. Lakshmi,S and Shanmugapriya,S ,Stochastic Model for endocrine stress responses in chronic fatigue syndrome ,Bioscience Research Bulletin V0l-24,No-2,2008,P-63-67. Martz,H.F. and Waller, R.A., Bayesian Reliability Analysis, John Wiley, New York,1982.The book contains important information for Bayesian analysis in Reliability theory, including a good chapter on empirical Bayes methods. Miller ,R.G., Jr., Survival Analysis ,John Wiley,New York,1981.Treats mainly non –parametric methods in aconcise manner. Shi H, Segaloff DL : A role for increased lutropin/ choriogondotropin receptor (LHR) gene transcription in the follitropin –stimulated induction of the LHR in granulose cells. Mol Endocrinol 9: 734,1995. www.ijera.com 46 | P a g e