Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Turlapati Raseswari"'
Autor:
Pratibha Nallari, Venkata Padmalatha, Murthy Kanakavalli, Nalini J. Gupta, Hridesh Dixit, Baidyanath Chakrabarty, Durgadatta Tosh, Lalji Singh, Turlapati Raseswari, Lakshmi Rao, Mamata Deenadayal, Bineet Panda
Publikováno v:
Gynecological Endocrinology. 27:572-578
Present study was designed for carrying out the mutational analysis of the entire Androgen receptor (AR) gene including two microsatellite (CAG)n, (GGN)n, promoter region in cases of premature ovarian failure (POF) and primary amenorrhea (PA).Previou
Autor:
Venkata Padmalatha, Pratibha Nallari, Baidyanath Chakrabarthy, Kanakavalli Murthy, Anil Kumar Kapu, Mamata Deenadayal, Lalji Singh, Turlapati Raseswari, Nalini J. Gupta, Lakshmi Rao, Hridesh Dixit, Durgadutta Tosh, Bineet Panda
Publikováno v:
Reproductive BioMedicine Online. 20:724-740
Premature ovarian failure (POF) is unexplained amenorrhoea (>6 months), increased FSH (>20 IU/l) and LH occurring before 40 years. Several genes are reported as having significance in POF, including genes governing regulation of the hypothalamic-pitu
Autor:
Rao Kandukuri, Lakshmi, Padmalatha, Venkata, Kanakavalli, Murthy, Turlapati, Raseswari, Swapna, Mangalipally, Vidyadhari, Metuku, Saranaya, Govindaraghavan, Himaja, Kattera, Deenadayal, Mamata, Kumar Sethi, Bipin, Deb, Prasun, Gupta, Nalini, Chakraborthy, Baidyanath, Nallari, Pratibha, Singh, Lalji
Publikováno v:
Case Reports in Genetics.
Premature ovarian failure is defined as the loss of functional follicles below the age of 40 years and the incidence of this abnormality is 0.1% among the 30–40 years age group. Unexplained POF is clinically recognized as amenorrhoea (>6 months) wi
Autor:
Saranya G, Aswini S, N. Chandra, Lalji S, Kanakavalli M Kulashekaran, Venkata O Padmalatha, Lakshmi Rao Kandukuri, Jagan Singh Meena, Turlapati Raseswari, Durgadatta T
Publikováno v:
Molecular Cytogenetics, Vol 4, Iss 1, p 21 (2011)
Molecular Cytogenetics
Molecular Cytogenetics
Chromosome rearrangements involving telomeres have been established as one of the major causes of idiopathic mental retardation/developmental delay. This case of 7p partial trisomy syndrome in a 3-year-old female child presenting with developmental d
Autor:
Lakshmi, Rao, Venkata, Suryanarayana, Murthy, Kanakavalli, Venkata, Padmalatha, Turlapati, Raseswari, Nallari, Pratibha, Mamata, Deenadayal, Lalji, Singh
Publikováno v:
Reproductive biomedicine online. 17(4)
Male DNA of recognized fetal origin can be detected in the maternal circulation many years after delivery. It is referred to as fetal microchimerism, and is thus a possible explanation for the existence of low-level Y chromosome mosaicisms. Employing
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Autor:
Glenn M. Marshall, Stefan Hüttelmaier, Knut Krohn, Daniel R. Carter, Turlapati Raseswari, Tao Liu, Jessica L. Bell, Bernard Atmadibrata
Publikováno v:
Cancer Research. 74:3103-3103
Previous studies have shown chromosomal 17q21-ter amplification in neuroblastoma is both a common and highly prognostic event. The oncogene, insulin-like growth factor-2 mRNA-binding protein 1 (IGF2BP1), is located near the proximal edge of this ampl
Autor:
Kandukuri, Lakshmi Rao, Padmalatha, Venkata, Kanakavalli, Murthy, Turlapati, Raseswari, Swapna, Mangalipally, Vidyadhari, Metuku, Saranaya, Govindaraghavan, Himaja, Kattera, Deenadayal, Mamata, Sethi, Bipin Kumar, Deb, Prasun, Gupta, Nalini, Chakraborthy, Baidyanath, Nallari, Pratibha, Singh, Lalji
Publikováno v:
Case Reports in Genetics; 2012, p1-8, 8p