SOX3 is required during the formation of the hypothalamo-pituitary axis

K Rizzoti, S Brunelli, D Carmignac, PQ Thomas… - Nature …, 2004 - nature.com
The pituitary develops from the interaction of the infundibulum, a region of the ventral
diencephalon, and Rathke's pouch, a derivative of oral ectoderm. Postnatally, its secretory …

[HTML][HTML] Activation of Toll-like receptor 7/8 encoded by the X chromosome alters sperm motility and provides a novel simple technology for sexing sperm

T Umehara, N Tsujita, M Shimada - PLoS biology, 2019 - journals.plos.org
In most mammals, the male to female sex ratio of offspring is about 50% because half of the
sperm contain either the Y chromosome or X chromosome. In mice, the Y chromosome …

A simple sperm-sexing method that activates TLR7/8 on X sperm for the efficient production of sexed mouse or cattle embryos

T Umehara, N Tsujita, Z Zhu, M Ikedo, M Shimada - Nature Protocols, 2020 - nature.com
The preferred sex of livestock differs among breeders; for example, dairy farmers prefer
female calves for the production of milk, whereas cattle meat producers often prefer males …

The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome

ML Delbridge, PA Lingenfelter, CM Disteche… - Nature …, 1999 - nature.com
Fig. 1 FISH localization of the cloned RBMY-like sequence from Xq26. We labelled 2 kb of
YAC genomic sequence containing exons 6− 12 with biotin and hybridized it to human male …

Schistosomus reflexus syndrome: a heritable defect in ruminants

KW Laughton, KRS Fisher… - Anatomia, histologia …, 2005 - Wiley Online Library
Schistosomus reflexus (SR) is a rare and fatal congenital disorder. Primarily observed in
ruminants, its defining features include spinal inversion, exposure of the abdominal viscera …

RBMX gene is essential for brain development in zebrafish

E Tsend‐Ayush, LA O'Sullivan… - Developmental …, 2005 - Wiley Online Library
The human RBMX gene was discovered recently through its homology to the
spermatogenesis candidate gene RBMY. Its position on the human X chromosome suggests …

Identification and characterization of an Xq26–q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes

FA Hol, MT Schepens, SEC van Beersum, E Redolfi… - Genomics, 2000 - Elsevier
We investigated a family with a duplication, dup (X) q26–q27, that was present in two
brothers, their mother, and their maternal grandmother. The brothers carrying the duplication …

RBMY evolved on the Y chromosome from a ubiquitously transcribed XY identical gene

S Mazeyrat, N Saut, MG Mattei, MJ Mitchell - Nature genetics, 1999 - nature.com
1999 Nature America Inc.• http://genetics. nature. com correspondence nature genetics•
volume 22• july 1999 225 however, RBMY has been on the Y chromosome since before the …

Combined pentalogy of Cantrell with tetralogy of Fallot, gallbladder agenesis, and polysplenia: a case report

S Bittmann, H Ulus, A Springer - Journal of pediatric surgery, 2004 - Elsevier
Combined pentalogy of cantrell with tetralogy of fallot, gallbladder agenesis, and polysplenia: a
case report - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books …

[HTML][HTML] X Chromosomal short tandem repeat polymorphisms near the phosphoglycerate kinase gene in men with chronic prostatitis

DE Riley, JN Krieger - Biochimica et Biophysica Acta (BBA)-Molecular …, 2002 - Elsevier
Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) causes substantial morbidity
afflicting approximately 10% of adult males. Treatment is often empirical and ineffective …