Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Kristina Lundin"'
Autor:
Kristina Lundin, Andrea Biloglav, Linda Olsson, Setareh Safavi, Kajsa Paulsson, Bertil Johansson
Publikováno v:
Genes, Chromosomes and Cancer. 55:472-479
Single nucleotide polymorphism (SNP) arrays are increasingly being used in clinical routine for genetic analysis of pediatric B-cell precursor acute lymphoblastic leukemias (BCP ALL). Because constitutional DNA is not readily available as a control a
Association between polymorphisms in the prostate-specific antigen (PSA) promoter and release of PSA
Autor:
Johan Malm, Yvonne Lundberg Giwercman, Hans Lilja, Aleksander Giwercman, Christer Halldén, Kristina Lundin, Charlotta Sävblom
Variations in serum prostate-specific antigen (PSA) have been ascribed to A/G nucleotide polymorphisms located at -158 bp (rs266882) and -4643 bp (rs925013), relative to the transcription start site within the promoter of the PSA gene. PSA is also an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa3bcf7ac1a46d97a4442d08e322a1d5
https://doi.org/10.1111/j.1365-2605.2008.00882.x
https://doi.org/10.1111/j.1365-2605.2008.00882.x
Autor:
Magdalena Cwikiel, Eva Cavallin-Ståhl, Jakob Eberhard, Kristina Lundin, Aleksander Giwercman, Olof Ståhl, Yvonne Lundberg Giwercman
Publikováno v:
European Journal of Cancer. 40:2152-2158
Sex hormones and/or gonadotropins may play a crucial role in the development of testicular germ cell cancer (TGCC). A direct link between this malignancy and endocrine factors has not been confirmed. We tested whether CAG and GGN repeats of the andro
Autor:
Magdalena Cwikiel, Aleksander Giwercman, Jakob Eberhard, Olof Ståhl, Per Flodgren, Yvonne Lundberg Giwercman, Kristina Lundin, Eva Cavallin-Ståhl
Publikováno v:
Human Reproduction. 19:1418-1425
in Undetermined BACKGROUND: Testicular cancer (TC) patients have a high survival rate, and the question of post-therapy recovery of sperm production and its dependence on genetic predisposition is of major interest. METHODS: Ejaculates were obtained
Autor:
Jonas Richthoff, Kristina Lundin, Sten A. Ivarsson, Yvonne Lundberg Giwercman, Aleksander Giwercman
Publikováno v:
Hormone Research in Paediatrics. 61:58-62
Background: An absent or dysfunctional androgen receptor (AR) in 46,XY individuals is the most common cause of various degrees of undermasculinization. Therefore, we routinely perform sequencing of the AR gene in all cases with suspected androgen ins
Autor:
Carsten Rose, Maria Henningson, Christian Ingvar, Kristina Lundin, Maria Hietala, Helena Jernström
Publikováno v:
British Journal of Cancer; 105(11), pp 1676-1683 (2011)
British Journal of Cancer
British Journal of Cancer
Background:The androgen receptor (AR) is frequently expressed in breast cancers. The AR genotype may affect disease-free survival and response to endocrine therapy.Methods:In all, 634 women undergoing breast cancer surgery between 2002 and 2008 were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4d74af5f7472e553719033dc2380fd5
http://lup.lub.lu.se/record/2200097/file/2256477.pdf
http://lup.lub.lu.se/record/2200097/file/2256477.pdf
Publikováno v:
European journal of endocrinology. 155(2)
Background: The human androgen receptor (AR) gene contains two polymorphisms of CAG and GGN repeats respectively. The GGN repeat function is still largely unknown and to date there are no in vivo data on this segment with respect to the general popul
Publikováno v:
Molecular and Cellular Endocrinology; 264(1-2), pp 184-187 (2007)
Superior androgen receptor (AR) function in subjects carrying a GGN repeat length of 23 (GGN23) has been indicated in vivo. Therefore, the activity of the AR carrying GGN23 combined with CAG22 was compared to the AR with GGN10, 24 and 27, respectivel
Publikováno v:
The Journal of clinical endocrinology and metabolism. 91(8)
Background: The androgen receptor A645D mutation has been described in one patient with ambiguous genitalia and one boy with normal phenotype. Objective: Because of this phenotypic variation, we screened a cohort of men from the general population (n
Autor:
Kristina Lundin, Yasir Ruhayel, Yvonne Lundberg Giwercman, Aleksander Giwercman, Elin L. Aschim, Agneta Nordenskjöld, Tom Grotmol, Trine B. Haugen
Publikováno v:
The Journal of clinical endocrinology and metabolism. 89(10)
Although sufficient androgen receptor (AR) function is crucial for normal male sexual differentiation, single-point mutations in the AR gene are infrequent in the two most common male congenital malformations, hypospadias and cryptorchidism. Because