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A time-dependent, two-step binding mode of the nitro dye flavianic acid to trypsin in acid media

Brazilian journal of medical and biological research, 2001-08, Vol.34 (8), p.1047-1054

2001

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Calorimetric versus Growth Microbial Analysis of Cellulase Enzymes Acting on Cellulose

Applied and Environmental Microbiology, 1987-12, Vol.53 (12), p.2935-2941

1987

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Human red cell hemolysis rates in the subsecond to seconds range. An analysis

Biophysical journal, 1977-11, Vol.20 (2), p.181-191

1977

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Colloidal Gold Cytochemistry of Endo-1,4-β-Glucanase, 1,4-β-D-Glucan Cellobiohydrolase, and Endo-1,4-β-Xylanase: Ultrastructure of Sound and Decayed Birch Wood

Applied and Environmental Microbiology, 1989-09, Vol.55 (9), p.2293-2301

1989

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Stoichiometry of Wheat Germ Agglutinin as a Morphology Controlling Agent and as a Morphology Protective Agent for the Human Erythrocyte

The Journal of cell biology, 1980-06, Vol.85 (3), p.534-548

1980

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Stoichiometry of wheat germ agglutinin as a morphology controlling agent and as a morphology controlling agent and as a morphology protective agent for the human erythrocyte

The Journal of cell biology, 1980-06, Vol.85 (3), p.534-548

1980

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Rapid Flow Titration and the Rate of the Acid Expansion of Bovine Serum Albumin

Journal of physical chemistry (1952), 1959-06, Vol.63 (6), p.1025-1026

1959

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Discriminating activities of DEAD-Box Helicase 41 from myeloid malignancy-associated germline variants by genetic rescue

Leukemia, 2023-01, Vol.37 (1), p.235-239

2023

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Autosomal Dominant Congenital Cataract Associated with a Missense Mutation in the Human Alpha Crystallin Gene CRYAA

Human molecular genetics, 1998-03, Vol.7 (3), p.471-474

1998

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Molecular Genetics of Human Blue Cone Monochromacy

Science (American Association for the Advancement of Science), 1989-08, Vol.245 (4920), p.831-838

1989

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A Second Gene for Cerulean Cataracts Maps to the β Crystallin Region on Chromosome 22

Genomics (San Diego, Calif.), 1996-08, Vol.35 (3), p.539-542

1996

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Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families

American journal of human genetics, 1990-04, Vol.46 (4), p.652-660

1990

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Familial Cutaneous Malignant Melanoma: Autosomal Dominant Trait Possibly Linked to the Rh Locus

Proceedings of the National Academy of Sciences - PNAS, 1983-10, Vol.80 (19), p.6071-6075

1983

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Human chromosome variation: the discriminatory power of Q-band heteromorphism (variant) analysis in distinguishing between individuals, with specific application to cases of questionable paternity

American journal of human genetics, 1986-02, Vol.38 (2), p.235-252

1986

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Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man

Science (American Association for the Advancement of Science), 1970-10, Vol.170 (3953), p.85-87

1970

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Gene Dosage: Evidence for Assignment of Erythrocyte Acid Phosphatase Locus to Chromosome 2

Proceedings of the National Academy of Sciences - PNAS, 1975-11, Vol.72 (11), p.4526-4530

1975

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Factor IXPortland: a nonsense mutation (CGA to TGA) resulting in hemophilia B

American journal of human genetics, 1989-04, Vol.44 (4), p.567-569

1989

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A locus for the nystagmus-associated form of episodic ataxia maps to an 11-cM region on chromosome 19p

American journal of human genetics, 1995-07, Vol.57 (1), p.182-185

1995

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Human chromosome variations: The discriminatory power of Q-band heteromorphism (variant) analysis in distinguishing between individuals, with specific application to cases of questionable paternity

American journal of human genetics, 1986-01, Vol.38 (2), p.235-252

1986

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Acquired immunodeficiency syndrome-associated non-Hodgkin's lymphomas and other malignancies in patients with hemophilia

Blood, 1993-04, Vol.81 (7), p.1889-1897

1993

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Factor IX sub(Portland): A nonsense mutation (CGA to TGA) resulting in hemophilia B

American journal of human genetics, 1989-01, Vol.44 (4), p.567-569

1989

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Dyschondrosteosis and Madelung's deformity. Report of three kindreds and review of the literature

Clinical orthopaedics and related research, 1976-05 (116), p.24-28

1976

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Mannosidosis in three brothers--a review of the literature

Medicine (Baltimore), 1977-07, Vol.56 (4), p.335-348

1977

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Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-)

Journal of medical genetics, 1972-09, Vol.9 (3), p.280-286

1972

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A time-dependent, two-step binding mode of the nitro dye flavianic acid to trypsin in acid media

Calorimetric versus Growth Microbial Analysis of Cellulase Enzymes Acting on Cellulose

Human red cell hemolysis rates in the subsecond to seconds range. An analysis

Colloidal Gold Cytochemistry of Endo-1,4-β-Glucanase, 1,4-β-D-Glucan Cellobiohydrolase, and Endo-1,4-β-Xylanase: Ultrastructure of Sound and Decayed Birch Wood

Stoichiometry of Wheat Germ Agglutinin as a Morphology Controlling Agent and as a Morphology Protective Agent for the Human Erythrocyte

Stoichiometry of wheat germ agglutinin as a morphology controlling agent and as a morphology controlling agent and as a morphology protective agent for the human erythrocyte

Rapid Flow Titration and the Rate of the Acid Expansion of Bovine Serum Albumin

Discriminating activities of DEAD-Box Helicase 41 from myeloid malignancy-associated germline variants by genetic rescue

Autosomal Dominant Congenital Cataract Associated with a Missense Mutation in the Human Alpha Crystallin Gene CRYAA

Acquired Immunodeficiency Syndrome-Associated Non-Hodgkin’s Lymphomas and Other Malignancies in Patients With Hemophilia

Molecular Genetics of Human Blue Cone Monochromacy

A Second Gene for Cerulean Cataracts Maps to the β Crystallin Region on Chromosome 22

Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families

Familial Cutaneous Malignant Melanoma: Autosomal Dominant Trait Possibly Linked to the Rh Locus

Human chromosome variation: the discriminatory power of Q-band heteromorphism (variant) analysis in distinguishing between individuals, with specific application to cases of questionable paternity

Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man

Gene Dosage: Evidence for Assignment of Erythrocyte Acid Phosphatase Locus to Chromosome 2

Factor IXPortland: a nonsense mutation (CGA to TGA) resulting in hemophilia B

A locus for the nystagmus-associated form of episodic ataxia maps to an 11-cM region on chromosome 19p

Human chromosome variations: The discriminatory power of Q-band heteromorphism (variant) analysis in distinguishing between individuals, with specific application to cases of questionable paternity

Acquired immunodeficiency syndrome-associated non-Hodgkin's lymphomas and other malignancies in patients with hemophilia

Factor IX sub(Portland): A nonsense mutation (CGA to TGA) resulting in hemophilia B

Dyschondrosteosis and Madelung's deformity. Report of three kindreds and review of the literature

Mannosidosis in three brothers--a review of the literature

Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-)

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