Darius J. Devlin

Darius J. Devlin
Baylor College of Medicine | BCM · Department of Pathology & Immunology

Ph.D. in Translational Biology & Molecular Medicine

About

13
Publications
5,729
Reads
How we measure 'reads'
A 'read' is counted each time someone views a publication summary (such as the title, abstract, and list of authors), clicks on a figure, or views or downloads the full-text. Learn more
109
Citations
Citations since 2017
13 Research Items
109 Citations
2017201820192020202120222023010203040
2017201820192020202120222023010203040
2017201820192020202120222023010203040
2017201820192020202120222023010203040
Introduction

Publications

Publications (13)
Article
Full-text available
Objective To evaluate the feasibility of generating a center-specific embryo morphokinetic algorithm by time-lapse microscopy to predict clinical pregnancy rate. Design Retrospective cohort analysis Setting Academic fertility clinic in a tertiary hospital setting Patients Patients who underwent in vitro fertilization with embryos that underwent...
Article
Full-text available
As the world population continues to increase to unsustainable levels, the importance of birth control and the development of new contraceptives are emerging. To date, male contraceptive options have been lagging behind those available to women, and those few options available are not satisfactory to everyone. To solve this problem, we have been se...
Article
Full-text available
Developing a safe and effective male contraceptive remains a challenge in the field of medical science. Molecules that selectively target the male reproductive tract and whose targets are indispensable for male reproductive function serve among the best candidates for a novel non-hormonal male contraceptive method. To determine the function of thes...
Article
CRISPR/Cas9-based genome editing in mice uncovers 13 testis-or epididymis-enriched genes individually dispensable for male reproduction Running title: Genome editing reveals dispensable testis-and epididymis-enriched genes Summary sentence: Thirteen testis-or epididymis-enriched genes are individually dispensable for male fertility based on phenoty...
Article
Full-text available
Family with sequence similarity 170 members A and B (FAM170A and FAM170B) are two testis-specific, paralogous proteins that share 31% amino acid identity and are conserved throughout mammals. While in vitro experiments in previous literature suggested that FAM170B, an acrosome-localized protein, plays a role in the mouse sperm acrosome reaction and...
Article
ECF systems are new transporters that take up various vitamins, cobalt, or nickel with a high affinity. Here, we establish the GAS SiaFGH proteins as a new ECF module that imports heme and demonstrate its importance in virulence. SiaFGH is the first heme ECF system described in bacteria. We identified homologous systems in the genomes of related pa...
Article
Full-text available
Globozoospermia (sperm with an abnormally round head shape) and asthenozoospermia (defective sperm motility) are known causes of male infertility in human patients. Despite many studies, the molecular details of the globozoospermia etiology are still poorly understood. Serine-rich single pass membrane protein 1 (Ssmem1) is a conserved testis-specif...
Article
Receptor accessory protein 6 (REEP6) is a member of the REEP/Ypt-interacting protein (Yip) family that we recently identified as essential for normal endoplasmic reticulum (ER) homeostasis and protein trafficking in the retina of mice and humans. Interestingly, in addition to the loss of REEP6 in our knockout (KO) mouse model recapitulating the ret...
Article
Full-text available
Background Spermatozoa become competent for fertilization during transit through the epididymis. As spermatozoa from the proximal caudal epididymis can fertilize eggs, proteins from the caput and corpus epididymis are required for sperm maturation. Objectives Microarray analysis identified that more than 17,000 genes are expressed in the epididymi...

Network

Cited By

Projects

Project (1)
Project
I am working to identify proteins that are crucial for spermatogenesis that can be inhibited by small molecules to give a contraceptive effect that is reversible. These targets are implicated from CRISPR/Cas9-mediated knockout mice that have an infertility phenotype.