Manan Khan
Overview
Explore the profile of Manan Khan including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
147
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Recent Articles
1.
Ali A, Unar A, Muhammad Z, Dil S, Zhang B, Sadaf H, et al.
J Assist Reprod Genet
. 2023 Oct;
41(1):109-120.
PMID: 37831349
Purpose: Asthenozoospermia is an important cause of male infertility, and the most serious type is characterized by multiple morphological abnormalities of the sperm flagella (MMAF). However, the precise etiology of...
2.
Jiao Y, Fan S, Jabeen N, Zhang H, Khan R, Murtaza G, et al.
Sci Bull (Beijing)
. 2023 Feb;
65(24):2120-2129.
PMID: 36732965
Meiosis is pivotal for sexual reproduction and fertility. Meiotic programmed DNA double-strand breaks (DSBs) initiate homologous recombination, ensuring faithful chromosome segregation and generation of gametes. However, few studies have focused...
3.
Khan R, Zaman Q, Chen J, Khan M, Ma A, Zhou J, et al.
Front Endocrinol (Lausanne)
. 2021 Dec;
12:765639.
PMID: 34867808
Male infertility is a prevalent disorder distressing an estimated 70 million people worldwide. Despite continued progress in understanding the causes of male infertility, idiopathic sperm abnormalities such as multiple morphological...
4.
Shah B, Khan R, Shah W, Aftab A, Khan M, Dil S, et al.
Mamm Genome
. 2021 Jun;
32(5):364-370.
PMID: 34076717
Several genes have been reported to be involved in spermatogenesis but their functional importance in male fertility is yet needed to be elucidated. Therefore, in current research, we focused to...
5.
Hussain H, Murtaza G, Jiang X, Khan R, Khan M, Kakakhel M, et al.
Horm Res Paediatr
. 2019 Apr;
91(1):9-16.
PMID: 30947225
Background: Congenital hypogonadotropic hypogonadism (CHH) is a heterogeneous disorder characterized by delayed or loss of puberty and infertility due to functional deficiency in the hypothalamic gonadotropin-releasing hormone (GnRH). CHH can...
6.
Huang Z, Khan M, Xu J, Khan T, Ma H, Khan R, et al.
Sci China Life Sci
. 2019 Mar;
62(4):544-552.
PMID: 30919279
The balanced actions between ubiquitination and deubiquitination precisely control the levels of various proteins vital for spermatogenesis. Ubiquitin-specific processing proteases (USPs) are the largest family of deubiquitinatingenzymes(DUBs), containing more than...
7.
Yin H, Ma H, Hussain S, Zhang H, Xie X, Jiang L, et al.
Genet Med
. 2018 Aug;
21(1):266.
PMID: 30158692
Hao Win, Hui Ma and Sajjad Hussain were incorrectly affiliated to 'Department of Radiation Oncology, The Houston Methodist Research Institute, Houston, TX 77030 USA'. These authors should only have been...
8.
Khan T, Khan M, Yousaf A, Khan S, Naeem M, Shah A, et al.
J Hum Genet
. 2018 Jul;
63(10):1071-1076.
PMID: 30033443
Hereditary leukonychia (also known as porcelain nails or white nails) is a genetic disorder. It may exist as an isolated feature or associated with other cutaneous or systemic disorders. Although...
9.
Yin H, Ma H, Hussain S, Zhang H, Xie X, Jiang L, et al.
Genet Med
. 2018 Jun;
21(1):62-70.
PMID: 29895858
Purpose: Fanconi anemia (FA) genes play important roles in spermatogenesis. In mice, disruption of Fancm impairs male fertility and testicular integrity, but whether FANCM pathogenic variants (PV) similarly affect fertility...
10.
Khan M, Jabeen N, Khan T, Hussain H, Ali A, Khan R, et al.
Sci Rep
. 2018 Mar;
8(1):4975.
PMID: 29563520
There are more than 2300 genes that are predominantly expressed in mouse testes. The role of hundreds of these genes has been studied in mouse spermatogenesis but still there are...