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Yves Lachance

Researcher at Laval University

Publications -  14
Citations -  1562

Yves Lachance is an academic researcher from Laval University. The author has contributed to research in topics: Complementary DNA & Gene. The author has an hindex of 12, co-authored 14 publications receiving 1537 citations.

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Structure and Expression of a New Complementary DNA Encoding the almost Exclusive 3β-Hydroxysteroid Dehydrogenase/Δ5-Δ4-lsomerase in Human Adrenals and Gonads

TL;DR: A second type of cDNA clone (arbitrarily designated type II) encoding 3βHSD is reported after screening of a human adrenal λgt22A library, which predicts a protein of 371 amino acids with a calculated molecular mass of 41,921 daltons.
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Full Length cDNA Structure and Deduced Amino Acid Sequence of Human β-Hydroxy-5-Ene Steroid Dehydrogenase

TL;DR: Polyclonal antibodies raised against 3β-hydroxysteroid dehydrogenase isolated from human placenta were used to screen a λgt11 expression cDNA library from the same tissue, deducing the protein deduced from cDNA sequences contains 372 amino acids.
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Characterization of cDNAs for Human Estradiol 17β-Dehydrogenase and Assignment of the Gene to Chromosome 17: Evidence of two mRNA Species with Distinct 5′-Termini in Human Placenta

TL;DR: Since E2DH is the enzyme required for the formation of 17 beta-estradiol, the availability of the cDNA encoding the enzyme should permit a detailed investigation of the factors regulating the expression and activity of this crucial enzyme, in both normal and malignant tissues, especially breast cancer.
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Structure of two in tandem human 17β-hydroxysteroid dehydrogenase genes

TL;DR: The complete exon and intron sequences of the two genes as well as their 5′ and 3′-flanking regions are determined and provide the basis for a better understanding of the molecular mechanisms involved in 17β-HSD deficiency and peripheral sex steroid metabolism.
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Structure of the Human Type II 3β-Hydroxysteroid Dehydrogenase/Δ5-Δ4 Isomerase (3β-HSD) Gene: Adrenal and Gonadal Specificity

TL;DR: In this article, the authors described the isolation and complete sequence of the corresponding type II 3 beta-HSD gene, which is the form most likely responsible for human 3 Beta-HHSD deficiency.