نتایج جستجو برای: xy

تعداد نتایج: 7750  

الماسی, محمد امین, بابازاده بدوستانی, علیرضا,

Background and purpose: In humans, SRY (sex-determining region of the Y chromosome) is the major gene for the sex determination which is found in normal XY males and rarely in XX males, and it is absent from normal XX females and from many XY females. There are several methods which can indicate a male genotype by amplification of SRY gene. The aim of this study was identification of the SRY ge...

2013
Jérôme Bertrand Benoît R. Kloeckner

We extend the geometric study of the Wasserstein space W2(X) of a simply connected, negatively curved metric space X by investigating which pairs of boundary points can be linked by a geodesic, when X is a tree. Let X be a Hadamard space, by which we mean that X is a complete globally CAT(0), locally compact metric space. Mainly, X is a space where triangles are “thin”: points on the opposite s...

2006
E. BOĎA

Let P := k [X,Y, Z] be a polynomial ring over an algebraic closed field k and (X, Y , Z, XY Z, XY Z ) · k [X,Y, Z] an (X,Y, Z)-primary ideal in P , (m, n, l, a, b, c, d, e, f are integers). The ideal Q=(X, Y , Z, XY Z, XY Z ) ·R is (X,Y, Z) · R-primary ideal in the local ring R = k [X,Y, Z](x,y,z). In this short note we give a formula for the calculation of Samuel multiplicity e0(Q,R) of the id...

Journal: :Endocrinology 2013
Xuqi Chen Rebecca McClusky Yuichiro Itoh Karen Reue Arthur P Arnold

Three different models of MF1 strain mice were studied to measure the effects of gonadal secretions and sex chromosome type and number on body weight and composition, and on related metabolic variables such as glucose homeostasis, feeding, and activity. The 3 genetic models varied sex chromosome complement in different ways, as follows: 1) "four core genotypes" mice, comprising XX and XY gonada...

Journal: :Physical review. B, Condensed matter 1989
Harris Aharony

The randomly diluted resistor network and XY model at low temperature T are studied near the d-dimensional percolation threshold using the ɛ expansion, where ɛ=6-d. The series expansion of the inverse susceptibility in powers of T for the XY model is identical to that of the appropriate resistive inverse susceptibility in powers of σ0−1, where σ0 is the conductance of a bond. However, the tempe...

2015
Vu Chi Dung Bui Phuong Thao Nguyen Ngoc Khanh Can Thi Bich Ngoc Maki Fukami

A rare form of the 46,XY disorders of sex development (DSD), 5a-reductase deficiency was first described in patients with pseudovaginal perineoscrotal hypospadias, microphallus, and cryptorchid testes in 1974 by Imperato. This undervirilization in the male is due to an alteration in the 5a-reductase type 2 gene (SRD5A2), which encodes for 5areductase activity. Our registry of 750 patients with ...

Journal: :Development 1996
C M Nagamine C Carlisle

The Y chromosome from certain populations of M. m. domesticus is incapable of normal testis determination in the B6 inbred strain resulting in XY hermaphrodites or XY females (XY(DOM) sex reversal). B6 consomic strains have been developed with either transient (B6-Y(AKR)) or severe (B6-Y(TIR)) XY(DOM) sex reversal. We report that a point mutation, the dominant white spotting oncogene allele, Ki...

Journal: :Development 1994
M Steinmann-Zwicky

In Drosophila, the sex of germ cells is determined by cell-autonomous and inductive signals. XY germ cells autonomously enter spermatogenesis when developing in a female host. In contrast, XX germ cells non-autonomously become spermatogenic when developing in a male host. In first instar larvae with two X chromosomes, XX germ cells enter the female or the male pathway depending on the presence ...

Journal: :Crystals 2022

Laser powder bed fusion (LPBF)-manufactured Sc-Zr-modified Al–Mg alloy (Scalmalloy) has a bimodal microstructure comprising coarse grains (CGs) in the hot melt pool area and ultrafine (UFGs) along boundaries (MPBs). Owing to these microstructural features, an increase MPBs can UFGs, leading enhanced mechanical properties. However, effects of LPBF process parameters, especially laser scan strate...

Journal: :Journal of medical genetics 1977
F Mollica G Sorge L Pavone

A child with many symptoms of trisomy 22 syndrome is described. The child showed a 46,XY/47,XY,+22 chromosome constitution. This is the first reported case of a trisome 22 phenotype with such a mosaic karyotype.

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