Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Fareeha Zulfiqar"'
Autor:
Hannah C. Zierden, Kevin DeLong, Fareeha Zulfiqar, Jairo Ortiz Ortiz, Victoria Laney, Sabrine Bensouda, Nicole Hernández, Thuy M. Hoang, Samuel K. Lai, Justin Hanes, Anne E. Burke, Laura M. Ensign
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 13 (2023)
IntroductionMucus in the female reproductive tract acts as a barrier that traps and eliminates pathogens and foreign particles via steric and adhesive interactions. During pregnancy, mucus protects the uterine environment from ascension of pathogens
Externí odkaz:
https://doaj.org/article/af1906c97a1b44b09b9d0f4244b31288
Autor:
Kevin DeLong, Sabrine Bensouda, Fareeha Zulfiqar, Hannah C. Zierden, Thuy M. Hoang, Alison G. Abraham, Jenell S. Coleman, Richard A. Cone, Patti E. Gravitt, Craig W. Hendrix, Edward J. Fuchs, Charlotte A. Gaydos, Ethel D. Weld, Laura M. Ensign
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 9 (2019)
The success of fecal microbiota transplant (FMT) in treating recurrent Clostridioides difficile infection has led to growing excitement about the potential of using transplanted human material as a therapy for a wide range of diseases and conditions
Externí odkaz:
https://doaj.org/article/fdea386915214f668e71e3f6716de0b1
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e67393 (2013)
Inflammatory bowel disease (IBD) is a common disease, includes Crohn's disease (CD) and ulcerative colitis (UC), and is determined by altered gut bacterial populations and aberrant host immune response. Peptidoglycan recognition proteins (PGLYRP) are
Externí odkaz:
https://doaj.org/article/2c1ef4959664456e896551c2114995b0
Autor:
Ian M. MacDonald, Xueshan Xiao, Fareeha Zulfiqar, Paul A. Sieving, S. Amer Riazuddin, Qingjiong Zhang, J. Fielding Hejtmancik, Sheikh Riazuddin, Zahoor Ahmad, R.C. Caruso
Publikováno v:
Human Genetics. 122:293-299
Mutation in the PROM1 gene previously has been identified in one family with retinal degeneration for which neither ERG recordings nor detailed information about visual impairment is available. A large family with multiple individuals affected by ret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8acf4b898c4a9f0d854efd7ae8853df
https://doi.org/10.1007/s00439-007-0395-2
https://doi.org/10.1007/s00439-007-0395-2
Autor:
S. Amer Riazuddin, Paul A. Sieving, J. Fielding Hejtmancik, Sheikh Riazuddin, Fareeha Zulfiqar, Qingjiong Zhang, Radha Ayyagari, Farooq Sabar, R.C. Caruso, Xueshan Xiao
Publikováno v:
Human Genetics. 118:356-365
A severe form of autosomal recessive retinitis pigmentosa (arRP) was identified in a large Pakistani family ascertained in the Punjab province of Pakistan. All affected individuals in the family had night blindness in early childhood, early complete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e4b3e6d6d1364a1e6e101188dbb3c2f
https://doi.org/10.1007/s00439-005-0054-4
https://doi.org/10.1007/s00439-005-0054-4
Autor:
Dipika Gupta, Fareeha Zulfiqar, Iztok Hozo, Roman Dziarski, Roy A. Mariuzza, Sneha Rangarajan
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e67393 (2013)
PLoS ONE
PLoS ONE
Inflammatory bowel disease (IBD) is a common disease, includes Crohn's disease (CD) and ulcerative colitis (UC), and is determined by altered gut bacterial populations and aberrant host immune response. Peptidoglycan recognition proteins (PGLYRP) are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cf09e0ad4d8d3dc415cb3b28a15d173
http://europepmc.org/articles/PMC3686734?pdf=render
http://europepmc.org/articles/PMC3686734?pdf=render
Autor:
William J. Kimberling, Amber Shahzadi, Ahmed Rebai, Peter Söderkvist, Zeineb Benzina, Fareeha Zulfiqar, Houria Dhouib, Sheikh Riazuddin, Abdelmonem Ghorbel, Hammadi Ayadi, Mounira Hmani-Aifa
Publikováno v:
European journal of human genetics : EJHG. 17(4)
Autosomal recessive retinitis pigmentosa (ARRP) is a genetically heterogeneous disorder. ARRP could be associated with extraocular manifestations that define specific syndromes such as Usher syndrome (USH) characterized by retinal degeneration and co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::170e7bfcab609c566bfe708a9a5979da
https://pubmed.ncbi.nlm.nih.gov/18854872
https://pubmed.ncbi.nlm.nih.gov/18854872
Autor:
S Amer, Riazuddin, Fareeha, Zulfiqar, Qingjiong, Zhang, Wenliang, Yao, Shouling, Li, Xiaodong, Jiao, Amber, Shahzadi, Muhammad, Amer, Muhammad, Iqbal, Tayyab, Hussnain, Paul A, Sieving, Sheikh, Riazuddin, J Fielding, Hejtmancik
Publikováno v:
Molecular vision. 12
To localize and identify the gene and mutations causing autosomal recessive retinitis pigmentosa (RP) in consanguineous Pakistani families.Families were ascertained and patients underwent complete ophthalmological examinations. Blood samples were col
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6057d533ec78c099d9d3e2ec7b7d76a1
https://pubmed.ncbi.nlm.nih.gov/17110911
https://pubmed.ncbi.nlm.nih.gov/17110911
Publisher Summary A study was conducted to identify genes causing autosomal recessive retinitis pigmentosa (arRP). In this study, 50 families showing autosomal recessive mode of inheritance were screened for their linkage to the already reported cand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9eab635cb4871e03e4f649a79448564
https://doi.org/10.1016/b978-044452806-3/50003-2
https://doi.org/10.1016/b978-044452806-3/50003-2
Autor:
Akhtar Ali, Clara Sattler de Sousa e Brito, Corinna Burger, Régis Cartier, J. Michael O'Donnell, Hubert Doucet, Ole Döring, Merle Fairhurst, Rebecca S. Feinberg, Josué Feingold, Agomoni Ganguli, Christian Hervé, Johannes Huber, E. Douglas Lewandowski, Jean-François Lutz, Rashid Mehmood, Thomas Meyer, Hervé de Milleville, G. Moutel, Anne-Sophie Paquez, Eric Racine, Muhammad Ramzan, Regina Reszka, Assad Riaz, Sheikh Riazuddin, Markus Schmidt, Jacques-Aurélien Sergent, Andrea T. Thalmann, Fareeha Zulfiqar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fa37a8fc97d47ed9e4339a55dd5cc04
https://doi.org/10.1016/b978-044452806-3/50002-0
https://doi.org/10.1016/b978-044452806-3/50002-0