Results 71 to 80 of about 63,568 (308)

Comprehensive genotype-phenotype correlation in lissencephaly

open access: yesQuantitative Imaging in Medicine and Surgery, 2018
Malformations of cortical development (MCD) are a heterogenous group of disorders with diverse genotypic and phenotypic variations. Lissencephaly is a subtype of MCD caused by defect in neuronal migration, which occurs between 12 and 24 weeks of gestation.
Ai Peng, Tan   +2 more
openaire   +3 more sources

Deciphering transcriptional plasticity in pancreatic ductal adenocarcinoma reveals alterations in sensory neuron innervation

open access: yesMolecular Oncology, EarlyView.
Pancreatic sensory neurons innervating healthy and PDAC tissue were retrogradely labeled and profiled by single‐cell RNA sequencing. Tumor‐associated innervation showed a dominant neurofilament‐positive subtype, altered mitochondrial gene signatures, and reduced non‐peptidergic neurons.
Elena Genova   +14 more
wiley   +1 more source

Nephronophthisis: A review of genotype–phenotype correlation [PDF]

open access: yesNephrology, 2018
ABSTRACTNephronophthisis is an autosomal recessive cystic kidney disease and one of the most common genetic disorders causing end‐stage renal disease in children. Nephronophthisis is a genetically heterogenous disorder with more than 25 identified genes.
Luo, Fenglan, Tao, Yu‐Hong
openaire   +2 more sources

Differential expression of cancer‐related genes supports prediction of poor response to first‐line treatments in T‐ALL pediatric patients with high minimal residual disease

open access: yesMolecular Oncology, EarlyView.
In the present work, we have identified a transcriptional signature based on the differential expression of six genes (BCL2&MAST4, HSH2D&LAT2, METRN&PITPNM2) that would facilitate the early detection of T‐cell acute lymphoblastic leukemia (T‐ALL) patients prone to a poor treatment response and could be implemented at diagnosis, along with other risk ...
Antonio Lahera   +11 more
wiley   +1 more source

PHENOTYPIC AND GENOTYPIC CORRELATION COEFFICIENTS FOR SOME YIELD AND FIBER QUALITY TRAITS OF SEGREGATING POPULATIOS (F2, F3 AND F4) IN SOME EGYPTIAN COTTON CROSSES [PDF]

open access: yesJournal of Plant Production, 2012
    The present study was undertaken with a view to determine the extent of relationship between seed cotton yield and other economic traits of F2, F3 and F4 generations in the two Egyptian cotton crosses i.e., cross I [({Giza 89 x Giza 85} x {Giza 86 x ...
E. El-Hashash, M. Srour
doaj   +1 more source

Genotypic variation in Pneumocystis jirovecii isolates in Britain

open access: yes, 2005
Background: Pneumocystis jirovecii is the cause of Pneumocystis pneumonia (PCP) in immunosuppressed humans. Asymptomatic colonisation with P jirovecii may occur in patients with minor immunosuppression or chronic lung disease.
Davies, RJ   +6 more
core   +1 more source

CD47 promotes mitogen‐activated protein kinase and epithelial‐to‐mesenchymal transition molecular programs to drive prometastatic phenotypes in non‐small cell lung cancer

open access: yesMolecular Oncology, EarlyView.
Beyond its role in immune evasion, this study identified that CD47 drives tumor‐intrinsic signaling in non‐small cell lung cancer (NSCLC). Transcriptomic profiling and functional studies revealed that CD47 regulates cell adhesion, migration, and metastasis through an ERK–EMT signaling axis.
Asa P.Y. Lau   +8 more
wiley   +1 more source

STUDIES ON SOME WHEAT CROSSES UNDER SALINE CONDITIONS [PDF]

open access: yesJournal of Plant Production, 2004
Five F4 and Fs selected families of five bread wheat crosses were evaluated at Ras Sudr Research station of Desert Research Center, south- Sinai Governorate in two growing seasons 2001 I 2002 and 2002 I 2003 winter under salinity of irrigation water ...
S. Omar, A . Hassan,
doaj   +1 more source

Interaction of HS1BP3 with cortactin modulates TKS5 localisation, cell secretion and cancer malignancy

open access: yesMolecular Oncology, EarlyView.
Here, we demonstrate that HS1BP3 interacts with Cortactin through a proline‐rich region (PRR3.1) and show that this interaction, and HS1BP3 itself, promote cancer cell proliferation and invasion. Inhibition of this interaction leads to build‐up of TKS5 in multivesicular endosomes and altered secretion of CD63 and CD9, providing an explanation for the ...
Arja Arnesen Løchen   +9 more
wiley   +1 more source

Finding novel vulnerabilities of hypomorphic BRCA1 alleles

open access: yesMolecular Oncology, EarlyView.
Synthetic lethality screens performed to identify novel vulnerabilities often model complete gene loss, thereby overlooking patient‐derived hypomorphic mutations. In this study, we have performed genome‐wide CRISPR screens on BRCA1 hypomorphic mutations, showing BRCA1I26A behaves like wild‐type, while BRCA1R1699Q mimics deficiency. Furthermore, we have
Anne Schreuder   +10 more
wiley   +1 more source

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