Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Leena Rawal"'
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 21, Iss 1, Pp 1-10 (2023)
Abstract Background The dynamics of mammalian follicular development and atresia is an intricate process involving the cell-cell communication mediated by secreted ovarian factors. These interactions are critical for oocyte development and regulation
Externí odkaz:
https://doaj.org/article/80b54831cb764844bd7ea46f311a35b0
Autor:
Shiba Ranjan Mishra, Leena Rawal, Moneeb A. K. Othman, Atul Thatai, Aditi Sarkar, Vandana Lal, Saurabh Kumar Bhattacharya
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-5 (2021)
Abstract Background The translocation t(8;21)(q22;q22) is one of the most frequent chromosomal abnormalities associated with acute myeloid leukemia (AML) sub type M2. About 3–5 % of cases with additional chromosomal abnormalities, including structu
Externí odkaz:
https://doaj.org/article/568317231d6c4e6e9a135e040aac856e
Publikováno v:
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 209-215 (2020)
Background: Human reproduction is the most intricate event as ~ 20% of human pregnancies end in miscarriages for which chromosomal anomalies are a common factor. The chromosomal variations associated with reproductive failures include translocations,
Externí odkaz:
https://doaj.org/article/0fdbd24b1c23423c9e9aaf2f1546b3b2
Publikováno v:
Cellular Physiology and Biochemistry, Vol 46, Iss 2, Pp 505-519 (2018)
Background/Aims: The major histocompatibility complex (MHC) categorized into three (I, II and III) classes elicits the immunogenic response by presenting exogenous peptides to T cells. The MHC-II DM is composed of DMα and DMβ, two polypeptide chain
Externí odkaz:
https://doaj.org/article/63e69467b98442ce97f48d4349f81dc1
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0127993 (2015)
Molecular interactions between mesenchymal-derived Keratinocyte growth factor (KGF) and Kit ligand (KITLG) are essential for follicular development. These factors are expressed by theca and granulosa cells. We determined full length coding sequence o
Externí odkaz:
https://doaj.org/article/805aea1e88124a0f8bce1d2242e0cb0f
Publikováno v:
Journal of Human Reproductive Sciences
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 209-215 (2020)
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 209-215 (2020)
Background: Human reproduction is the most intricate event as ~ 20% of human pregnancies end in miscarriages for which chromosomal anomalies are a common factor. The chromosomal variations associated with reproductive failures include translocations,
Autor:
Aditi Sarkar, Moneeb A.K. Othman, Shiba Ranjan Mishra, Vandana Lal, Leena Rawal, Atul Thatai, Saurabh Bhattacharya
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-5 (2021)
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-5 (2021)
Background The translocation t(8;21)(q22;q22) is one of the most frequent chromosomal abnormalities associated with acute myeloid leukemia (AML) sub type M2. About 3–5 % of cases with additional chromosomal abnormalities, including structural and n
Publikováno v:
Journal of Cellular Biochemistry. 118:4254-4266
The major histocompatibility complex (MHC) with its three classes represents a cluster of tightly linked genes with defined immunological and non-immunological functions. The DM, a MHC class II molecule is formed by the non-covalent association of DM
Publikováno v:
Journal of Genetics. 94:677-687
Sex chromosome-related anomalies engender plethora of conditions leading to male infertility. Hypogonadotropic hypogonadism (HH) is a rare but well-known cause of male infertility. Present study was conducted to ascertain possible consensus on the al
Autor:
Leena Rawal, Sher Ali
This book highlights selected current data and its relevance in the human health care system, offering a fundamental primer on genetics and human health.With the advent of new high-throughput technologies (for the whole genome including exome sequenc