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Content Provider : Complementary Index Subject : genetic mutation Subject : nucleotide sequencing Filter by : Keyword Sort Order : Publication Date Acsending

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Academic Journal

Evidence of genetic heterogeneity in Huntington's chorea.

Authors : Wallace, D. C.; Hall, A. C.

Subjects: AGE distribution; AGGRESSION (Psychology); ALCOHOLISMAUSTRALIA

Source: Journal of Neurology, Neurosurgery & Psychiatry; Dec1972, Vol. 35 Issue 6, p789-800, 12p, 4 Charts

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News

RESEARCH NOTES: Scientists identify gene that increases risk of common cancers.

Authors : Raymond, Chris

Subjects: CANCER genetics; GENETIC mutationUNITED States

Source: Chronicle of Higher Education; 12/5/90, Vol. 37 Issue 14, pA8, 2p

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News

Genetic cause is found for some case of Alzheimer's disease.

Authors : Wheeler, David L.

Subjects: GENETICS of Alzheimer's disease; CHROMOSOMES; GENETIC mutation

Source: Chronicle of Higher Education; 2/27/91, Vol. 37 Issue 24, pA8-A8, 1/6p

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Academic Journal

A genetic model compatible with a dimensional view of schizophrenia.

Authors : Roberts, David; Claridge, Gordon; Roberts, D

Subjects: PREFACES & forewords; SCHIZOPHRENIA; FAMILIES & psychology

Source: British Journal of Psychiatry; Apr91, Vol. 158, p451-456, 6p, 2 Diagrams

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Academic Journal

Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease.

Authors : Planté-Bordeneuve, V; Davis, M B; Maraganore, D M

Subjects: AGE distribution; ALLELES; COMPARATIVE studiesIRELAND

Source: Journal of Neurology, Neurosurgery & Psychiatry; Aug1994, Vol. 57 Issue 8, p911-913, 3p, 4 Charts

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Academic Journal

Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus.

Authors : De Michele, G; Filla, A; Cavalcanti, F

Subjects: AGE distribution; BIOPSY; CARRIER proteins

Source: Journal of Neurology, Neurosurgery & Psychiatry; Aug1994, Vol. 57 Issue 8, p977-979, 3p

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Academic Journal

Elongation on the amino-terminal part of stefin B decreases inhibition of cathepsin H.

Authors : Jerala, Roman; Kroon-Žitko, Louisa; Popovič, Tatjana

Subjects: CYSTEINE proteinases; AMINO acids; ESCHERICHIA coli

Source: European Journal of Biochemistry; 9/15/94, Vol. 224 Issue 3, p797-802, 6p

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Academic Journal

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and...

Authors : Muscatelli, Francoise; Strom, Tim M.

Subjects: GENETIC mutation; HYPOGONADISM

Source: Nature; 12/15/1994, Vol. 372 Issue 6507, p672, 5p, 2 Diagrams, 2 Charts

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Academic Journal

Hereditary Protein C Deficiency: The Australian Experience.

Authors : Doig, Rowan G.; Begley, C. Glenn; McGrath, Katherine M.

Subjects: THROMBOSIS; GENETIC disorders; POLYMERASE chain reaction

Source: Clinical & Applied Thrombosis/Hemostasis; Winter1995, Vol. 1 Issue 1, p49-54, 6p, 3 Black and White Photographs, 2 Charts

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Academic Journal

Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles.

Authors : Orrell, R W; King, A W; Hilton, D A

Subjects: AMYOTROPHIC lateral sclerosis; BRAIN; COMPARATIVE studies

Source: Journal of Neurology, Neurosurgery & Psychiatry; Sep1995, Vol. 59 Issue 3, p266-270, 5p, 3 Black and White Photographs, 1 Diagram

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