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  Encyclopedia of Keywords > Paroxysmal Nocturnal Hemoglobinuria > Molecular Basis   Michael Charnine

Keywords and Sections
INHERITED MICROCYTIC ANEMIA
BACTERIAL OUTER MEMBRANE PERMEABILITY
RESISTANCE
REVIEW
PHOSPHORYLATION
PHENOMENON
POORLY
COMPLEX
CRYSTAL STRUCTURE
SICKLE CELL DISEASE
CHEMICAL PROPERTIES
CELLS
PNH
DEFICIENCY
CELLULAR RESPIRATION
DEEPER UNDERSTANDING
INHERITED DISEASE
GENETIC DISEASE
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
HORMONE ACTION
CELL BIOLOGY
UNKNOWN
PATHOGENESIS
GENETICS
GROWTH HORMONE DEFICIENCY
HUMANS
UNDERSTANDING
GENETIC
CYSTIC FIBROSIS
DISEASE
POLYCYTHEMIA VERA
TREATMENT
FAMILIAL HYPERCHOLESTEROLEMIA
MUTATIONS
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA
MOLECULAR BASIS
Review of Short Phrases and Links

    This Review contains major "Molecular Basis"- related terms, short phrases and links grouped together in the form of Encyclopedia article.

Inherited Microcytic Anemia

  1. Molecular basis of inherited microcytic anemia due.

Bacterial Outer Membrane Permeability

  1. Nikaido H: Molecular basis of bacterial outer membrane permeability revisited.

Resistance

  1. Molecular basis of resistance of influenza A viruses to amantadine. (Web site)

Review

  1. Review [Evolution and host variation of the canine parvovirus: molecular basis for the development of a new virus] [Berl Munch Tierarztl Wochenschr. (Web site)

Phosphorylation

  1. This observation now raises the questions of how phosphorylation is started, and then what is the molecular basis for consecutive phosphorylation. (Web site)

Phenomenon

  1. Louis Pasteur deduced in 1848 that this phenomenon has a molecular basis[2].

Poorly

  1. The molecular basis of resistance to Fusarium ear blight in cereal species is poorly understood.

Complex

  1. The molecular basis of haemochromatosis has proved more complex than expected. (Web site)
  2. Recently, the molecular basis for atovaquone resistance in P. jirovecii was modeled in the cytochrome bc 1 complex of Saccharomyces cerevisiae (21, 38).

Crystal Structure

  1. Crystal structure of a stable dimer reveals the molecular basis of serpin polymerization. (Web site)

Sickle Cell Disease

  1. This made sickle cell disease the first genetic disorder whose molecular basis was known. (Web site)

Chemical Properties

  1. Biological diversity has its molecular basis in carbon's ability to form a huge number of molecules with particular shapes and chemical properties.

Cells

  1. The molecular basis of the posterior is not known, however, the accumulation of cells eventually results in the posterior marginal zone (PMZ).
  2. But we know very little about the molecular basis of pluripotency and what controls the range of cells into which a stem cell can differentiate.

Pnh

  1. In the early seventies it was shown that PNH is a clonal disease; and in the nineties the molecular basis of the PNH abnormality was elucidated. (Web site)

Deficiency

  1. We originally identified deficiency of the cellular protein LMAN1 (also known as ERGIC53) as the molecular basis of this disorder in 70 percent of patients.

Cellular Respiration

  1. Molecular biology is the scientific study of the molecular basis of life processes, including cellular respiration, excretion, and reproduction. (Web site)

Deeper Understanding

  1. It is equally crucial for a deeper understanding of the molecular basis of biodiversity and synteny. (Web site)

Inherited Disease

  1. The metabolic and molecular basis of inherited disease.

Genetic Disease

  1. Beginning in 1986, map-based gene discovery (positional cloning) became the leading method for elucidating the molecular basis of genetic disease. (Web site)

Familial Hypertrophic Cardiomyopathy

  1. A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.

Hormone Action

  1. CrossRef Medline Web of Science ↵ Yen PM (2001) Physiological and molecular basis of thyroid hormone action. (Web site)

Cell Biology

  1. Zumft, W.G. (1997): Cell biology and molecular basis of denitrification.

Unknown

  1. Finding such predictors is particularly challenging because both the mechanism of lenalidomide activity in MDS and the molecular basis of MDS are unknown. (Web site)

Pathogenesis

  1. Little is known about the molecular basis of infection and pathogenesis of these viruses. (Web site)

Genetics

  1. The geneticist Joshua Lederberg (born 1925) was a pioneer in the study of bacteria and viruses to determine the chemical and molecular basis of genetics. (Web site)
  2. They are especially interested in the molecular basis of genetics and inheritance and the production of proteins. (Web site)

Growth Hormone Deficiency

  1. Forty years ago, when growth hormone (GH) first became available for use, the molecular basis for growth hormone deficiency (GHD) was entirely unknown.

Humans

  1. Describes molecular basis of gene structure and function to therapeutic gene cloning in humans.

Understanding

  1. In July 2004, he joined Dr. Collins' lab and immediately set his sights on understanding the molecular basis of progeria.

Genetic

  1. The SCNIR is an important resource for studies on the genetic and molecular basis for the disorders causing chronic neutropenia.

Cystic Fibrosis

  1. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis.

Disease

  1. Well-established mouse models of disease will be crucial for dissecting the molecular basis of complex disorders.

Polycythemia Vera

  1. Chen G, Prchal JT. Polycythemia vera and its molecular basis: an update. (Web site)

Treatment

  1. Quinolone-resistant Salmonella typhi in Viet Nam: molecular basis of resistance and clinical response to treatment. (Web site)
  2. Understanding of the molecular basis, clinical course, and treatment of HCM has increased substantially in the last decade.

Familial Hypercholesterolemia

  1. Update of the molecular basis of familial hypercholesterolemia in The Netherlands. (Web site)
  2. The molecular basis of familial hypercholesterolemia in the Netherlands.
  3. Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations. (Web site)

Mutations

  1. There are major problems associated with dissecting the molecular basis of even simple monogenic diseases caused by mutations in a single gene.
  2. Molecular basis of phenylketonuria and related hyperphenylalaninemias: mutations and polymorphisms in the human phenylalanine hydroxylase gene.

Paroxysmal Nocturnal Hemoglobinuria

  1. Molecular basis of the heterogeneity of expression of glycosyl phosphatidylinositol anchored proteins in paroxysmal nocturnal hemoglobinuria. (Web site)
  2. Rosse WF, Ware RE. The molecular basis of paroxysmal nocturnal hemoglobinuria [review].

Molecular Basis

  1. Blood 108: 1118-1119 [Full Text] Schafer, A. I. (2006). Molecular basis of the diagnosis and treatment of polycythemia vera and essential thrombocythemia.
  2. In the long run, study of the gene that is mutated in SDS should improve understanding of the molecular basis of disease.
  3. PMID 8100741. ^ Collinge J (2001). "Prion diseases of humans and animals: their causes and molecular basis".

Categories

  1. Paroxysmal Nocturnal Hemoglobinuria
  2. Familial Hypercholesterolemia
  3. Polycythemia Vera
  4. Health > Diseases > Genetic Disorders > Phenylketonuria
  5. Essential Thrombocythemia
  6. Books about "Molecular Basis" in Amazon.com

Book: Keywen Category Structure


  Short phrases about "Molecular Basis"
  Originally created: April 04, 2011.
  Links checked: February 21, 2013.
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