Zobrazeno 1 - 5
of 5
pro vyhledávání: '"M S Hamoud"'
Autor:
Nermine A. Osman, Hanan A. Abdel-Fattah, Balaram Ghosh, Yamini Bobde, Amany M. Ghanim, Sravani Pulya, Abdalla E. A. Hassan, Mohamed M. S. Hamoud
Publikováno v:
New Journal of Chemistry. 44:9671-9683
Most of the FDA approved histone deacetylase inhibitors (HDACi) contain hydroxamate as the zinc binding group (ZBG). Hydroxamates form strong electrostatic metal chelation with divalent zinc present in HDAC. This strong zinc chelation leads to unwant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15c3ab329456bea5176ff7e5f7f236a0
https://doi.org/10.1039/d0nj01274b
https://doi.org/10.1039/d0nj01274b
Publikováno v:
Medical Principles and Practice. 6:26-29
This is a case report of a Pakistani male neonate who died at the age of 46 days with pancreatic agenesis showing evidence of endocrine and exocrine insufficiency. The patient presented with persisten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40f227abeb4a4568e17d82e8e8fbcf89
https://doi.org/10.1159/000157420
https://doi.org/10.1159/000157420
Publikováno v:
Journal of perinatology : official journal of the California Perinatal Association. 23(7)
OBJECTIVES: To study the correlation of peak systolic velocity in the middle cerebral artery with hemoglobin concentration in fetuses at risk of anemia due to Rhesus isoimmunization. DESIGN: Peak systolic velocity of middle cerebral artery (MCA-PSV)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e58412d04be57a2fdfaea505a8bd92e7
https://pubmed.ncbi.nlm.nih.gov/14566348
https://pubmed.ncbi.nlm.nih.gov/14566348
Publikováno v:
American journal of medical genetics. 36(1)
We report on apparently nonmosaic trisomy 22 in a liveborn girl with multiple congenital anomalies. The abnormalities were growth retardation; microcephaly; hypertelorism; epicanthic folds; anti-mongoloid slant; apparently low-set, malformed ears; hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abe2c7cba28fa3ba22121be38e8b53a1
https://pubmed.ncbi.nlm.nih.gov/2185636
https://pubmed.ncbi.nlm.nih.gov/2185636
Publikováno v:
Journal of Medical Genetics. 28:138-139
We describe a newborn Arab male with defects similar to those seen in mice heterozygous for the mutant disorganisation (DS) gene. He had complete absence of the left lower limb including the left pelvic bone, hamartomas arising from the abdominal wal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e90c61f221611112723d5897290c000a
https://doi.org/10.1136/jmg.28.2.138
https://doi.org/10.1136/jmg.28.2.138