نتایج جستجو برای: xx

تعداد نتایج: 17148  

Journal: :Current Biology 2014
Laurent Boulanger Maëlle Pannetier Laurence Gall Aurélie Allais-Bonnet Maëva Elzaiat Daniel Le Bourhis Nathalie Daniel Christophe Richard Corinne Cotinot Norbert B. Ghyselinck Eric Pailhoux

The origin of sex reversal in XX goats homozygous for the polled intersex syndrome (PIS) mutation was unclear because of the complexity of the mutation that affects the transcription of both FOXL2 and several long noncoding RNAs (lncRNAs). Accumulating evidence suggested that FOXL2 could be the sole gene of the PIS locus responsible for XX sex reversal, the lncRNAs being involved in transcripti...

Journal: :The Journal of clinical endocrinology and metabolism 1999
M Lorentzon R Lorentzon T Bäckström P Nordström

The purpose of the present study was to investigate the influence of estrogen receptor alpha gene polymorphism and estradiol on height and bone density during and after puberty in males. Using the restriction enzymes XbaI and PvuII, the allelic variants XX, Xx, xx, PP, Pp, and pp were identified in 90 Caucasian boys 16.9+/-0.3 yr of age (mean +/- SD). Bone mineral density (BMD; g/cm2) of the to...

Journal: :American journal of medical genetics. Part A 2015
Capucine Hyon Sandra Chantot-Bastaraud Radu Harbuz Rakia Bhouri Nicolas Perrot Matthieu Peycelon Mathilde Sibony Sandra Rojo Xavier Piguel Frederic Bilan Brigitte Gilbert-Dussardier Alain Kitzis Ken McElreavey Jean-Pierre Siffroi Anu Bashamboo

Disorders of Sex Development (DSD) are a heterogeneous group of disorders affecting gonad and/or genito-urinary tract development and usually the endocrine-reproductive system. A genetic diagnosis is made in only around 20% of these cases. The genetic causes of 46,XX-SRY negative testicular DSD as well as ovotesticular DSD are poorly defined. Duplications involving a region located ∼600 kb upst...

Journal: :Journal of medical genetics 1998
S F Slaney I J Chalmers N A Affara L S Chitty

It is now well established that the differentiation of the primitive gonad into the testis during early human embryonic development depends on the presence of the SRY gene. However, the existence of total or partial sex reversal in 46,XX males with genetic mutations not linked to the Y chromosome suggests that several autosomal genes acting in association with SRY may contribute to normal devel...

2010
Jerrold M. Sadock

Aleut shows a remarkable alternation in its case and agreement patterns: roughly put, one pattern appears when a non-subject argument is syntactically unexpressed in a predicate, and the other pattern appears otherwise. This paper is devoted to an attempt to provide a coherent analysis for this alternation: the missing argument is analyzed as a pro which must move into a local relation with the...

Journal: :Journal of evolutionary biology 2013
L E Schwanz T Ezaz B Gruber A Georges

Evolutionary transitions between sex-determining mechanisms (SDMs) are an enigma. Among vertebrates, individual sex (male or female) is primarily determined by either genes (genotypic sex determination, GSD) or embryonic incubation temperature (temperature-dependent sex determination, TSD), and these mechanisms have undergone repeated evolutionary transitions. Despite this evolutionary lability...

Journal: :Cardiovascular research 2014
Jingyuan Li Xuqi Chen Rebecca McClusky Maureen Ruiz-Sundstrom Yuichiro Itoh Soban Umar Arthur P Arnold Mansoureh Eghbali

AIM Sex differences in coronary heart disease have been attributed to sex hormones, whereas the potential role of the sex chromosomes has been ignored so far. Here, we investigated the role of the sex chromosomes in causing sex differences in myocardial ischaemia/reperfusion (I/R) injury. METHODS AND RESULTS We used two unique mouse models, the 'four core genotypes' [XX mice with ovaries (XXF...

2014
Jun Ho Kim Eun Sun Jung Chul-Hyun Kim Hyeon Youn Hwa Rye Kim

PURPOSE The purpose of this study was to exam the association of body composition, flexibility, and injury risk to genetic polymorphisms including ACE ID, ACTN3 RX, and COL5A1 polymorphisms in ballet dancers in Korea. METHODS For the purpose of this study, elite ballerinas (n = 97) and normal female adults (n = 203) aged 18 to 39 were recruited and these participants were tested for body weig...

Journal: :The Tohoku journal of experimental medicine 1993
A Ishida Y Sawaishi A Goto Y Takahashi H Arai W Nakajima M Onozaki G Takada

A sister and a brother with 46, XX (46, XY), -21, +der (15) (q22.1; q22.1) mat were reported whose mother had a karyotype of 46, XX, t(15; 21)(q22.1; 22.1) and was phenotypically normal. Both sibs were mentally retarded and dysmorphic. Moreover, the sister had a holoprosencephaly with congenital hydrocephalus, and the brother showed congenital hydrocephalus.

Journal: :journal of physical & theoretical chemistry 2013
m. ghasemloo n. nikdel m. r. soltani m. firoozi f. soheilian

in this paper we studied the thermal negativity in a two-qubit xx spin ½ chain model and xxx spin1/2 chain model(isotropic heisenberg model)spin-1/2 chain subjected to an external magnetic field inz direction. we calculate analytical relation for the thermal negativity for two qubit xx and xxx spinchain models in the external magnetic field. effects of the magnetic field and temperature on then...

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