نتایج جستجو برای: humans 19th chromosome

تعداد نتایج: 310799  

Journal: :Cell 1997
Vincent Guacci Douglas Koshland Alexander Strunnikov

The S. cerevisiae MCD1 (mitotic chromosome determinant) gene was identified in genetic screens for genes important for chromosome structure. MCD1 is essential for viability and homologs are found from yeast to humans. Analysis of the mcd1 mutant and cell cycle-dependent expression pattern of Mcd1p suggest that this protein functions in chromosome morphogenesis from S phase through mitosis. The ...

Journal: :Bulletin of Symbolic Logic 1999
Volker Peckhaus

Doubt could be expressed that a special section on late 19th century mathematics, or, more specifically, on Victorian mathematics, was an appropriate place for a lecture on 19th century logic. Most 19th century scholars would have been of the opinion that philosophers are responsible for research on logic. On the other hand, the history of late 19th century logic indicates clearly a very dynami...

2017
Cheryl S. Rosenfeld

Brain sexual differentiation is orchestrated by precise coordination of sex steroid hormones. In some species, programming of select male brain regions is dependent upon aromatization of testosterone to estrogen. In mammals, these hormones surge during the organizational and activational periods that occur during perinatal development and adulthood, respectively. In various fish and reptiles, i...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Anna Y Aksenova Patricia W Greenwell Margaret Dominska Alexander A Shishkin Jane C Kim Thomas D Petes Sergei M Mirkin

Interstitial telomeric sequences (ITSs) are present in many eukaryotic genomes and are linked to genome instabilities and disease in humans. The mechanisms responsible for ITS-mediated genome instability are not understood in molecular detail. Here, we use a model Saccharomyces cerevisiae system to characterize genome instability mediated by yeast telomeric (Ytel) repeats embedded within an int...

Journal: :Seizure 2000
Youji Takeda Atsushi Baba Fumihiro Nakamura Masumi Ito Hiroshi Honma Tsukasa Koyama

An inverted duplication of chromosome 15 (inv dup[15] chromosome) is the most common supernumerary marker chromosome in humans. Inv dup(15) chromosomes are commonly associated with mental retardation, epilepsy, behavioral problems and structural malformations. Though epilepsies associated with inv dup(15) chromosomes are often intractable, there have been very few reports regarding the seizure ...

Journal: :Annual review of genetics 1996
J A Graves

Marsupials and monotremes, the mammals most distantly related to placental mammals, share essentially the same genome but show major variations in chromosome organization and function. Rules established for the mammalian genome by studies of human and mouse do not always apply to these distantly related mammals, and we must make new and more general laws. Some examples are contradictions to our...

Journal: :Pakistan languages and humanities review 2023

Matrimonial issues of the females have been core issue human life since history humans. Unmarriageable (2019) by Soniah Kamal and Jane Austen‘s Pride Prejudice in context Pakistani culture deal with marriages being concerned society capitalism. Cultural Materialism (CM) appeals to explore where is emerged materialistic thoughts. The current qualitative study explores matrimonial 19th 21st centu...

2013
Jenny C. Link Xuqi Chen Arthur P. Arnold Karen Reue

Obesity and associated metabolic diseases are sexually dimorphic. To provide better diagnosis and treatment for both sexes, it is of interest to identify the factors that underlie male/female differences in obesity. Traditionally, sexual dimorphism has been attributed to effects of gonadal hormones, which influence numerous metabolic processes. However, the XX/XY sex chromosome complement is an...

ژورنال: :مجله گیاهشناسی ایران 2007
سید محمود غفاری سیده باهره جوادی

رفتار میوزی برای اولین بار در زیر گونه crocus cancellatus subsp. damascenus (سیتوتیپ 2n=8a ) گزارش می شود. نتایج نشان می دهد که این زیر گونه (سیتوتیپ 2n=8a) دارای مجموعه کروموزومی 2n=8 و عدد گامتی n=4 می باشد. دو جفت کروموزوم به هستک متصل بود که تایید کننده حضور دو جفت کروموزوم قمردار در این زیر گونه می باشد. حضور یک عدد b کروموزوم در هر دو مرحله میوز و میتوز در این سیتوتیپ برای اولین بار گزارش...

2000

The purpose of the in vitro chromosomal aberration test is to identify agents that cause structural chromosome aberrations in cultured mammalian cells (1)(2)(3). Structural aberrations may be of two types, chromosome or chromatid. With the majority of chemical mutagens, induced aberrations are of the chromatid type, but chromosome-type aberrations also occur. An increase in polyploidy may indic...

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