Results 271 to 280 of about 939,325 (312)

MOLECULAR GENETICS OF MYOSIN

Annual Review of Biochemistry, 1987
PERSPECTIVES AND SUMMARY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . OVERVIEW OF MYOSIN STRUCTURE AND FUNCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . MHC Proteins " . . . . . . . . . . . . . . . , . . , . . . . . . . . . . . . . . . . . . . . . . . .
C P, Emerson, S I, Bernstein
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Dermatopathology and molecular genetics

Journal of the American Academy of Dermatology, 2008
The diagnosis of inherited skin diseases has been traditionally been based on clinical findings and occasionally on dermatopathology. Recent developments in molecular genetics have increased tremendously the diagnostic accuracy of genetic skin diseases, but also expanded the role of dermatopathology in the diagnosis and understanding of the ...
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Molecular Genetics and Breeding

2017
Molecular genetics is essentially the study of the mechanisms and effects of trait inheritance at the molecular level. Cytogenetic analysis—the study of the numbers, structure, and organization of the chromosomes packaging the DNA within the cell nucleus—is important for understanding evolution, genetics, epigenetics, genetic recombination, and nuclear
Soh, Aik Chin, Mayes, Sean, Roberts, Jeremy, Zaki, Noorhariza Mohd, Madon, Maria, Schwarzacher, Trude, Heslop-Harrison, Pat, Ithnin, Maizura Bint, Din, Amiruddin Mohd, Ramli, Umi Salamah, Othman, Abrizah, Zulkifli, Yaakub, Low Eng Ti, Leslie, Ong-Abdullah, Meilina, Singh, Rajinder, Teh, Chee Keng, Kwong, Qi Bin, Ong, Ail Ling, Mohamed, Mohaimi, Apparow, Sukganah, Chew, Fook Tim, Appleton, David Ross, Kulaveerasingam, Harikrishna, Teh, Huey Fang, Mebus, Katharina, Neoh, Bee Keat, Ooi, Tony Eng Keong, Wong, Yick Ching, Cros, David   +28 more
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Molecular genetics of migraine

Human Genetics, 2009
Migraine is an episodic neurovascular disorder that is clinically divided into two main subtypes that are based on the absence or presence of an aura: migraine without aura (MO) and migraine with aura (MA). Current molecular genetic insight into the pathophysiology of migraine predominantly comes from studies of a rare monogenic subtype of migraine ...
Boukje, de Vries, Rune R, Frants, Michel D, Ferrari, Arn M J M, van den Maagdenberg   +3 more
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Development of Molecular Genetics

cclm, 1999
AbstractHuman genetics has rapidly evolved from vague impression that descendants resemble their parents, to science which is now of utmost importance to the development of new principles and practice in medicine. It was only in the beginning of this century when it was suggested that chromosomes might carry genetic information.
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Molecular Genetics of Blindness

1994
Publisher Summary This chapter discusses molecular genetics of blindness. Although enormous progress has been made through the application of molecular techniques to the understanding of biological processes, a detailed understanding of development in complex structures has remained a challenge. In progressing toward this goal, the eye and retina, in
G C, Black, I W, Craig
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The Molecular Genetics of Cancer

Science, 1987
The search for genetic damage in neoplastic cells now occupies a central place in cancer research. Diverse examples of such damage are in hand, and they in turn hint at biochemical explanations for neoplastic growth. The way may be open to solve the riddles of how normal cells govern their replication and why cancer cells do not.
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Molecular genetics of meningiomas

2020
Comprehensive genomic studies of meningioma have offered important insights about the molecular mechanisms underlying this common brain tumor. The use of next-generation sequencing techniques has identified driver mutations in approximately 80% of benign sporadic lesions, as well as epigenetic, regulatory, and copy number events that are associated ...
Mark W, Youngblood, Murat, Günel
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Molecular genetics in neurology

Annals of Neurology, 1993
AbstractThere has been remarkable progress in the identification of mutations in genes that cause inherited neurological disorders. Abnormalities in the genes for Huntington disease, neurofibromatosis types 1 and 2, one form of familial amyotrophic lateral sclerosis, fragile X syndrome, myotonic dystrophy, Kennedy syndrome, Menkes disease, and several ...
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Molecular genetics of schizophrenia.

Clinical and experimental pharmacology & physiology, 2001
1. Schizophrenia is a chronic, disabling brain disease that affects approximately 1% of the world's population. It is characterized by delusions, hallucinations and formal thought disorder, together with a decline in socio-occupational functioning.
Mowry, B. J., Nancarrow, D. J.
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