Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84 [PDF]
The localization of chromosome 18 in human interphase nuclei is demonstrated by use of radioactive and nonradioactive in situ hybridization techniques with a DNA clone designated L1.84.
A. Brückner +33 more
core +1 more source
Streeter Dysplasia in Association with Cleft Palate: A Case Report [PDF]
Streeter dysplasia, a synonym of Amniotic Band Syndrome (ABS) is a wide spectrum of complex, controversial congenital anomalies. The disease varies in its severity which can range from a simple constriction ring to more severe and lethal forms like ...
Fairy Susan Varghese +2 more
doaj +1 more source
Amniotic band constriction leading to facial asymmetry
Rajesh Kumar Mandal, Anupam Das
doaj +2 more sources
Limb body wall complex, amniotic band sequence, or new syndrome caused by mutation in IQ Motif containing K (IQCK)? [PDF]
published_or_final_versio
Abe, Y +13 more
core +1 more source
Denudation of human amniotic membrane by a novel process and its characterisations for biomedical applications [PDF]
This study was aimed to investigate the suitability of a modified method to get decellularised human amniotic membrane (DHAM). The obtained membrane was subjected to physico-chemical and biological evaluations to validate its potential for biomedical ...
R. Kumar, R. Sripriya
core +1 more source
Cesarean scar defects and placental abnormalities – a 3 year survey study [PDF]
The placenta is an essential organ for embryonic and fetal development, ensuring nutrient uptake, gas exchange (via the mother\u27s blood supply), waste elimination, thermo-regulation, immunological and hormonal factors, etc.
Bacalbașa, Nicolae +2 more
core +4 more sources
Amniotic Band Syndrome, Perinatal Hospice, and Palliative Care versus Active Management
Introduction. Amniotic band syndrome and sequence are a relatively rare condition in which congenital anomalies occur as a result of the adherence and entrapment of fetal parts with coarse fibrous bands of the amniotic membrane.
Shadi Rezai +12 more
doaj +1 more source
Muc5ac mucin expression during rat skin development [PDF]
Some mucin genes have been detected during human embryonic and fetal organ development; however, little is known about mucin expression in epidermal development, neither in humans nor in other species. The present research was developed to explore Muc5ac
Barbeito, Claudio Gustavo +3 more
core +2 more sources
Steroid receptor co-activator interacting protein (SIP) mediates EGF-stimulated expression of the prostaglandin synthase COX2 and prostaglandin release in human myometrium [PDF]
Study hypothesis Steroid receptor coactivator interacting protein (SIP/KANK2) is involved in regulating the expression of the prostaglandin (PG)-endoperoxide synthase 2 (PTGS2; also known as cyclo-oxygenase 2, COX2) and PG release in human myometrium ...
Hudson, Claire A +2 more
core +2 more sources
Plasma rich in growth factors membrane as coadjuvant treatment in the surgery of ocular surface disorders [PDF]
This study received funding from the Ministry of Economy and Competitiveness of the Spanish Government, within the project denominated SURFEYE (reference RTC2014-2375-1)
Anitua, Eduardo +8 more
core +4 more sources

