プロフィール詳細

プロジェクトを作成

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Dr. Teka K.に依頼

United States

Reproductive Biologist with experience in genetics, stem cell, snRNAseq

プロフィール概要

PhD-trained geneticist with extensive experience in molecular genetics, genomics, and reproductive biology, combining strong scientific rigor with practical research and data-driven problem-solving. Proven expertise in experimental design, gene expression analysis, functional genomics, and interpretation of complex biological datasets across academic and translational research settings.

専門分野

• ☆ Molecular Biology
• ☆ Genetics
• ☆ Gene Expression Analysis
• ☆ Cell Biology
• ☆ Cell-Based Assays
• ☆ Cytochemistry
• ☆ Cytogenetics
• ☆ Cell Signaling Pathways
• ☆ Membrane Biology
• ☆ Gene Regulation
• ☆ Stem Cell Research
• ☆ Histology
• ☆ Biotechnology & Bioengineering
• ☆ Recombinant Protein Expression
• ☆ Cell Culture
• ☆ Primary Cells
• ☆ Cell Banking
• ☆ Large Scale Cell Culture
• ☆ Cell Surface Receptors
• ☆ 3D Cell Culture
• ☆ Tissue Engineering
• ☆ Artificial Organs
• ☆ Cytometry
• ☆ Endocrinology
• ☆ Reproductive Medicine

サービス

• Writing
• Research
• Consulting

Writing Translation

Research Scientific and Technical Research

Consulting Scientific and Technical Consulting

職務経験

Senior Scientest

University of Missouri

3月 2020 - 現在

学歴

PhD in Biology

University of Science and Technology of China

9月 2014 - 6月 2018

認定資格

• 認定資格の詳細は未入力です。

出版物

JOURNAL ARTICLE

Teka Khan, Sehee Choi, Sabrena Rutledge, Arun S. Seetharam, Laura C. Schulz, Geetu Tuteja, R. Michael Roberts (2025). Two classes of syncytiotrophoblast nuclei form following BAP-driven human pluripotent stem cell differentiation . Placenta.

Kinkade JA, Singh P, Verma M, Khan T, Ezashi T, Bivens NJ, Roberts RM, Joshi T, Rosenfeld CS (2024). Small and Long Non-Coding RNA Analysis for Human Trophoblast-Derived Extracellular Vesicles and Their Effect on the Transcriptome Profile of Human Neural Progenitor Cells . Cells.

Choi S, Khan T, Roberts RM, Schust DJ (2022). Leveraging Optimized Transcriptomic and Personalized Stem Cell Technologies to Better Understand Syncytialization Defects in Preeclampsia . Frontiers in genetics.

(2022). The product of BMP-directed differentiation protocols for human primed pluripotent stem cells is placental trophoblast and not amnion . STEM CELL REPORTS.

(2022). Leveraging Optimized Transcriptomic and Personalized Stem Cell Technologies to Better Understand Syncytialization Defects in Preeclampsia . FRONTIERS IN GENETICS.

Roberts RM, Ezashi T, Schulz LC, Sugimoto J, Schust DJ, Khan T, Zhou J (2021). Syncytins expressed in human placental trophoblast . Placenta.

(2021). A novel stop-gain mutation in <i>ARMC2</i> is associated with multiple morphological abnormalities of the sperm flagella . REPRODUCTIVE BIOMEDICINE ONLINE.

(2021). Single Nucleus RNA Sequence (snRNAseq) Analysis of the Spectrum of Trophoblast Lineages Generated From Human Pluripotent Stem Cells <i>in vitro</i> . FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY.

(2021). Syncytins expressed in human placental trophoblast . PLACENTA.

(2020). A <i>DNAH17</i> missense variant causes flagella destabilization and asthenozoospermia . JOURNAL OF EXPERIMENTAL MEDICINE.

(2019). A homozygous <i>FANCM</i> frameshift pathogenic variant causes male infertility . GENETICS IN MEDICINE.

(2019). A homozygous <i>FANCM</i> frameshift pathogenic variant causes male infertility (vol 21, pg 266, 2018) . GENETICS IN MEDICINE.

(2019). The deubiquitinating gene <i>Usp29</i> is dispensable for fertility in male mice . SCIENCE CHINA-LIFE SCIENCES.

(2019). Whole Exome Sequencing Revealed a Novel Nonsense Variant in the <i>GNRHR</i> Gene Causing Normosmic Hypogonadotropic Hypogonadism in a Pakistani Family . HORMONE RESEARCH IN PAEDIATRICS.

(2018). MOF influences meiotic expansion of H2AX phosphorylation and spermatogenesis in mice . PLOS GENETICS.

(2018). The evolutionarily conserved genes: <i>Tex37</i>, <i>Ccdc73</i>, <i>Prss55</i> and <i>Nxt2</i> are dispensable for fertility in mice . SCIENTIFIC REPORTS.

(2018). Whole exome sequencing identifies a novel dominant missense mutation underlying leukonychia in a Pakistani family . JOURNAL OF HUMAN GENETICS.

(2017). Histone acetyltransferase KAT8 is essential for mouse oocyte development by regulating reactive oxygen species levels . DEVELOPMENT.

(2017). RPL10L Is Required for Male Meiotic Division by Compensating for RPL10 during Meiotic Sex Chromosome Inactivation in Mice . CURRENT BIOLOGY.